Ligand source activities (1 row/activity)





Ligands (move mouse cursor over ligand name to see structure) Receptor Assay information Chemical information
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DOI

93149 216841 57 None -1 3 Human 6.0 pEC50 = 6 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 194 0 0 2 3.1 Cc1ccnc2c1ccc1cccnc12 10.1021/jm301121j
CHEMBL316589 216841 57 None -1 3 Human 6.0 pEC50 = 6 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 194 0 0 2 3.1 Cc1ccnc2c1ccc1cccnc12 10.1021/jm301121j
336912 174771 18 None None None Human 5.0 pEC50 = 5 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 240 2 2 4 1.8 OCc1ccc2ccc3ccc(CO)nc3c2n1 10.1021/jm301121j
CHEMBL2205802 174771 18 None None None Human 5.0 pEC50 = 5 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 240 2 2 4 1.8 OCc1ccc2ccc3ccc(CO)nc3c2n1 10.1021/jm301121j
2733927 174776 61 None -1 3 Human 5.0 pEC50 = 5 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 216 3 0 4 2.2 COc1ccnc(-c2cc(OC)ccn2)c1 10.1021/jm301121j
CHEMBL2205808 174776 61 None -1 3 Human 5.0 pEC50 = 5 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 216 3 0 4 2.2 COc1ccnc(-c2cc(OC)ccn2)c1 10.1021/jm301121j
667748 174773 59 None -3 2 Human 5.9 pEC50 = 5.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 267 2 0 3 3.9 Clc1cc(-c2ccccn2)nc(-c2ccccn2)c1 10.1021/jm301121j
CHEMBL2205805 174773 59 None -3 2 Human 5.9 pEC50 = 5.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 267 2 0 3 3.9 Clc1cc(-c2ccccn2)nc(-c2ccccn2)c1 10.1021/jm301121j
20445 174774 65 None -2 2 Human 4.9 pEC50 = 4.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1cccc(-c2cccc(C)n2)n1 10.1021/jm301121j
CHEMBL2205806 174774 65 None -2 2 Human 4.9 pEC50 = 4.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1cccc(-c2cccc(C)n2)n1 10.1021/jm301121j
667748 174773 59 None -3 2 Human 5.9 pEC50 = 5.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 267 2 0 3 3.9 Clc1cc(-c2ccccn2)nc(-c2ccccn2)c1 10.1021/jm301121j
CHEMBL2205805 174773 59 None -3 2 Human 5.9 pEC50 = 5.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 267 2 0 3 3.9 Clc1cc(-c2ccccn2)nc(-c2ccccn2)c1 10.1021/jm301121j
15783796 174779 3 None -1 3 Human 5.9 pEC50 = 5.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 194 0 0 2 3.1 Cc1cnc2c(ccc3cccnc32)c1 10.1021/jm301121j
CHEMBL2205810 174779 3 None -1 3 Human 5.9 pEC50 = 5.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 194 0 0 2 3.1 Cc1cnc2c(ccc3cccnc32)c1 10.1021/jm301121j
602123 174772 48 None None None Human 4.9 pEC50 = 4.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 236 2 0 4 2.4 O=Cc1ccc2ccc3ccc(C=O)nc3c2n1 10.1021/jm301121j
CHEMBL2205803 174772 48 None None None Human 4.9 pEC50 = 4.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 236 2 0 4 2.4 O=Cc1ccc2ccc3ccc(C=O)nc3c2n1 10.1021/jm301121j
20445 174774 65 None -2 2 Human 4.9 pEC50 = 4.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1cccc(-c2cccc(C)n2)n1 10.1021/jm301121j
CHEMBL2205806 174774 65 None -2 2 Human 4.9 pEC50 = 4.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1cccc(-c2cccc(C)n2)n1 10.1021/jm301121j
15783796 174779 3 None -1 3 Human 5.9 pEC50 = 5.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 194 0 0 2 3.1 Cc1cnc2c(ccc3cccnc32)c1 10.1021/jm301121j
CHEMBL2205810 174779 3 None -1 3 Human 5.9 pEC50 = 5.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 194 0 0 2 3.1 Cc1cnc2c(ccc3cccnc32)c1 10.1021/jm301121j
602123 174772 48 None None None Human 4.9 pEC50 = 4.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 236 2 0 4 2.4 O=Cc1ccc2ccc3ccc(C=O)nc3c2n1 10.1021/jm301121j
CHEMBL2205803 174772 48 None None None Human 4.9 pEC50 = 4.9 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 236 2 0 4 2.4 O=Cc1ccc2ccc3ccc(C=O)nc3c2n1 10.1021/jm301121j
74265 475171 73 None -3 3 Human 5.8 pEC50 = 5.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 236 0 0 2 4.0 Cc1cnc2c(ccc3c(C)c(C)cnc32)c1C 10.1021/jm301121j
CHEMBL99384 475171 73 None -3 3 Human 5.8 pEC50 = 5.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 236 0 0 2 4.0 Cc1cnc2c(ccc3c(C)c(C)cnc32)c1C 10.1021/jm301121j
353741 144287 4 None None None Human 4.8 pEC50 = 4.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 364 2 0 2 4.6 BrCc1ccc2ccc3ccc(CBr)nc3c2n1 10.1021/jm301121j
CHEMBL1976682 144287 4 None None None Human 4.8 pEC50 = 4.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 364 2 0 2 4.6 BrCc1ccc2ccc3ccc(CBr)nc3c2n1 10.1021/jm301121j
65237 275021 69 None 40 2 Human 5.8 pEC50 = 5.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1ccc2ccc3ccc(C)nc3c2n1 10.1021/jm301121j
CHEMBL375781 275021 69 None 40 2 Human 5.8 pEC50 = 5.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1ccc2ccc3ccc(C)nc3c2n1 10.1021/jm301121j
74265 475171 73 None -3 3 Human 5.8 pEC50 = 5.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 236 0 0 2 4.0 Cc1cnc2c(ccc3c(C)c(C)cnc32)c1C 10.1021/jm301121j
CHEMBL99384 475171 73 None -3 3 Human 5.8 pEC50 = 5.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 236 0 0 2 4.0 Cc1cnc2c(ccc3c(C)c(C)cnc32)c1C 10.1021/jm301121j
353741 144287 4 None None None Human 4.8 pEC50 = 4.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 364 2 0 2 4.6 BrCc1ccc2ccc3ccc(CBr)nc3c2n1 10.1021/jm301121j
CHEMBL1976682 144287 4 None None None Human 4.8 pEC50 = 4.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 364 2 0 2 4.6 BrCc1ccc2ccc3ccc(CBr)nc3c2n1 10.1021/jm301121j
15664 174775 66 None -3 3 Human 4.8 pEC50 = 4.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1ccc(-c2ccc(C)cn2)nc1 10.1021/jm301121j
5403 174775 66 None -3 3 Human 4.8 pEC50 = 4.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1ccc(-c2ccc(C)cn2)nc1 10.1021/jm301121j
CHEMBL2205807 174775 66 None -3 3 Human 4.8 pEC50 = 4.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1ccc(-c2ccc(C)cn2)nc1 10.1021/jm301121j
DB11932 174775 66 None -3 3 Human 4.8 pEC50 = 4.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1ccc(-c2ccc(C)cn2)nc1 10.1021/jm301121j
65237 275021 69 None 40 2 Human 5.8 pEC50 = 5.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1ccc2ccc3ccc(C)nc3c2n1 10.1021/jm301121j
CHEMBL375781 275021 69 None 40 2 Human 5.8 pEC50 = 5.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1ccc2ccc3ccc(C)nc3c2n1 10.1021/jm301121j
15664 174775 66 None -3 3 Human 4.8 pEC50 = 4.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1ccc(-c2ccc(C)cn2)nc1 10.1021/jm301121j
5403 174775 66 None -3 3 Human 4.8 pEC50 = 4.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1ccc(-c2ccc(C)cn2)nc1 10.1021/jm301121j
CHEMBL2205807 174775 66 None -3 3 Human 4.8 pEC50 = 4.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1ccc(-c2ccc(C)cn2)nc1 10.1021/jm301121j
DB11932 174775 66 None -3 3 Human 4.8 pEC50 = 4.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1ccc(-c2ccc(C)cn2)nc1 10.1021/jm301121j
72791 475073 52 None 1 2 Human 5.8 pEC50 = 5.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 194 0 0 2 3.1 Cc1cc2cccnc2c2ncccc12 10.1021/jm301121j
CHEMBL98682 475073 52 None 1 2 Human 5.8 pEC50 = 5.8 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 194 0 0 2 3.1 Cc1cc2cccnc2c2ncccc12 10.1021/jm301121j
77865 216919 57 None 1 2 Human 5.7 pEC50 = 5.7 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 214 0 0 2 3.4 Clc1cc2cccnc2c2ncccc12 10.1021/jm301121j
CHEMBL317115 216919 57 None 1 2 Human 5.7 pEC50 = 5.7 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 214 0 0 2 3.4 Clc1cc2cccnc2c2ncccc12 10.1021/jm301121j
72791 475073 52 None 1 2 Human 5.7 pEC50 = 5.7 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 194 0 0 2 3.1 Cc1cc2cccnc2c2ncccc12 10.1021/jm301121j
CHEMBL98682 475073 52 None 1 2 Human 5.7 pEC50 = 5.7 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 194 0 0 2 3.1 Cc1cc2cccnc2c2ncccc12 10.1021/jm301121j
12041800 468506 1 None None None Human 5.7 pEC50 = 5.7 Functional
Agonist activity at human CCR1 expressed in CHO cells by cellular dielectric spectroscopyAgonist activity at human CCR1 expressed in CHO cells by cellular dielectric spectroscopy
ChEMBL 410 7 2 4 6.4 Clc1ccc2c(NCCCCNc3ccnc4cc(Cl)ccc34)ccnc2c1 10.1016/j.bmcl.2011.11.014
CHEMBL66165 468506 1 None None None Human 5.7 pEC50 = 5.7 Functional
Agonist activity at human CCR1 expressed in CHO cells by cellular dielectric spectroscopyAgonist activity at human CCR1 expressed in CHO cells by cellular dielectric spectroscopy
ChEMBL 410 7 2 4 6.4 Clc1ccc2c(NCCCCNc3ccnc4cc(Cl)ccc34)ccnc2c1 10.1016/j.bmcl.2011.11.014
77865 216919 57 None 1 2 Human 5.7 pEC50 = 5.7 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 214 0 0 2 3.4 Clc1cc2cccnc2c2ncccc12 10.1021/jm301121j
CHEMBL317115 216919 57 None 1 2 Human 5.7 pEC50 = 5.7 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 214 0 0 2 3.4 Clc1cc2cccnc2c2ncccc12 10.1021/jm301121j
1474 310449 80 None -1 3 Human 4.5 pEC50 = 4.5 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 156 1 0 2 2.1 c1ccc(-c2ccccn2)nc1 10.1021/jm301121j
46936282 310449 80 None -1 3 Human 4.5 pEC50 = 4.5 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 156 1 0 2 2.1 c1ccc(-c2ccccn2)nc1 10.1021/jm301121j
CHEMBL39879 310449 80 None -1 3 Human 4.5 pEC50 = 4.5 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 156 1 0 2 2.1 c1ccc(-c2ccccn2)nc1 10.1021/jm301121j
DB03871 310449 80 None -1 3 Human 4.5 pEC50 = 4.5 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 156 1 0 2 2.1 c1ccc(-c2ccccn2)nc1 10.1021/jm301121j
1474 310449 80 None -1 3 Human 4.5 pEC50 = 4.5 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 156 1 0 2 2.1 c1ccc(-c2ccccn2)nc1 10.1021/jm301121j
46936282 310449 80 None -1 3 Human 4.5 pEC50 = 4.5 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 156 1 0 2 2.1 c1ccc(-c2ccccn2)nc1 10.1021/jm301121j
CHEMBL39879 310449 80 None -1 3 Human 4.5 pEC50 = 4.5 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 156 1 0 2 2.1 c1ccc(-c2ccccn2)nc1 10.1021/jm301121j
DB03871 310449 80 None -1 3 Human 4.5 pEC50 = 4.5 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 156 1 0 2 2.1 c1ccc(-c2ccccn2)nc1 10.1021/jm301121j
14338 18716 77 None -1 3 Human 5.4 pEC50 = 5.4 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1ccnc(-c2cc(C)ccn2)c1 10.1021/jm301121j
CHEMBL101165 18716 77 None -1 3 Human 5.4 pEC50 = 5.4 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1ccnc(-c2cc(C)ccn2)c1 10.1021/jm301121j
14338 18716 77 None -1 3 Human 5.4 pEC50 = 5.4 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1ccnc(-c2cc(C)ccn2)c1 10.1021/jm301121j
CHEMBL101165 18716 77 None -1 3 Human 5.4 pEC50 = 5.4 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 184 1 0 2 2.8 Cc1ccnc(-c2cc(C)ccn2)c1 10.1021/jm301121j
12987698 174777 3 None -2 3 Human 5.3 pEC50 = 5.3 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1cnc2c(ccc3cc(C)cnc32)c1 10.1021/jm301121j
CHEMBL2205809 174777 3 None -2 3 Human 5.3 pEC50 = 5.3 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1cnc2c(ccc3cc(C)cnc32)c1 10.1021/jm301121j
14434082 174770 20 None 1 3 Human 5.3 pEC50 = 5.3 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 236 2 0 4 2.4 O=Cc1ccnc2c1ccc1c(C=O)ccnc12 10.1021/jm301121j
CHEMBL2205801 174770 20 None 1 3 Human 5.3 pEC50 = 5.3 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 236 2 0 4 2.4 O=Cc1ccnc2c1ccc1c(C=O)ccnc12 10.1021/jm301121j
14434082 174770 20 None 1 3 Human 5.3 pEC50 = 5.3 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 236 2 0 4 2.4 O=Cc1ccnc2c1ccc1c(C=O)ccnc12 10.1021/jm301121j
CHEMBL2205801 174770 20 None 1 3 Human 5.3 pEC50 = 5.3 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 236 2 0 4 2.4 O=Cc1ccnc2c1ccc1c(C=O)ccnc12 10.1021/jm301121j
12987698 174777 3 None -2 3 Human 5.3 pEC50 = 5.3 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1cnc2c(ccc3cc(C)cnc32)c1 10.1021/jm301121j
CHEMBL2205809 174777 3 None -2 3 Human 5.3 pEC50 = 5.3 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1cnc2c(ccc3cc(C)cnc32)c1 10.1021/jm301121j
12425 11 80 None -1 3 Human 5.2 pEC50 = 5.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
1318 11 80 None -1 3 Human 5.2 pEC50 = 5.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
CHEMBL415879 11 80 None -1 3 Human 5.2 pEC50 = 5.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
DB02365 11 80 None -1 3 Human 5.2 pEC50 = 5.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
12425 11 80 None -1 3 Human 5.2 pEC50 = 5.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
1318 11 80 None -1 3 Human 5.2 pEC50 = 5.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
CHEMBL415879 11 80 None -1 3 Human 5.2 pEC50 = 5.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
DB02365 11 80 None -1 3 Human 5.2 pEC50 = 5.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
124734 473621 72 None -12 3 Human 4.2 pEC50 = 4.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 233 2 0 3 3.2 c1ccc(-c2cccc(-c3ccccn3)n2)nc1 10.1021/jm301121j
70848 473621 72 None -12 3 Human 4.2 pEC50 = 4.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 233 2 0 3 3.2 c1ccc(-c2cccc(-c3ccccn3)n2)nc1 10.1021/jm301121j
CHEMBL89445 473621 72 None -12 3 Human 4.2 pEC50 = 4.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 233 2 0 3 3.2 c1ccc(-c2cccc(-c3ccccn3)n2)nc1 10.1021/jm301121j
DB01912 473621 72 None -12 3 Human 4.2 pEC50 = 4.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 233 2 0 3 3.2 c1ccc(-c2cccc(-c3ccccn3)n2)nc1 10.1021/jm301121j
124734 473621 72 None -12 3 Human 4.2 pEC50 = 4.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 233 2 0 3 3.2 c1ccc(-c2cccc(-c3ccccn3)n2)nc1 10.1021/jm301121j
70848 473621 72 None -12 3 Human 4.2 pEC50 = 4.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 233 2 0 3 3.2 c1ccc(-c2cccc(-c3ccccn3)n2)nc1 10.1021/jm301121j
CHEMBL89445 473621 72 None -12 3 Human 4.2 pEC50 = 4.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 233 2 0 3 3.2 c1ccc(-c2cccc(-c3ccccn3)n2)nc1 10.1021/jm301121j
DB01912 473621 72 None -12 3 Human 4.2 pEC50 = 4.2 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 233 2 0 3 3.2 c1ccc(-c2cccc(-c3ccccn3)n2)nc1 10.1021/jm301121j
72792 433102 57 None -1 3 Human 6.1 pEC50 = 6.1 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1ccnc2c1ccc1c(C)ccnc12 10.1021/jm301121j
CHEMBL593442 433102 57 None -1 3 Human 6.1 pEC50 = 6.1 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1ccnc2c1ccc1c(C)ccnc12 10.1021/jm301121j
DB02586 433102 57 None -1 3 Human 6.1 pEC50 = 6.1 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1ccnc2c1ccc1c(C)ccnc12 10.1021/jm301121j
72792 433102 57 None -1 3 Human 6.1 pEC50 = 6.1 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1ccnc2c1ccc1c(C)ccnc12 10.1021/jm301121j
CHEMBL593442 433102 57 None -1 3 Human 6.1 pEC50 = 6.1 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1ccnc2c1ccc1c(C)ccnc12 10.1021/jm301121j
DB02586 433102 57 None -1 3 Human 6.1 pEC50 = 6.1 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
ChEMBL 208 0 0 2 3.4 Cc1ccnc2c1ccc1c(C)ccnc12 10.1021/jm301121j
11151928 352668 0 None 4 4 Human 9.8 pED50 = 9.8 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 2 hrs by microtiter format trans-well migration assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 2 hrs by microtiter format trans-well migration assay
ChEMBL 338 11 2 2 4.3 CCCCCCCCCCC(C)(C)C(=O)N[C@@H]1CCCCNC1=O 10.1021/jm900133w
11359715 352668 0 None 4 4 Human 9.8 pED50 = 9.8 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 2 hrs by microtiter format trans-well migration assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 2 hrs by microtiter format trans-well migration assay
ChEMBL 338 11 2 2 4.3 CCCCCCCCCCC(C)(C)C(=O)N[C@@H]1CCCCNC1=O 10.1021/jm900133w
CHEMBL468720 352668 0 None 4 4 Human 9.8 pED50 = 9.8 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 2 hrs by microtiter format trans-well migration assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 2 hrs by microtiter format trans-well migration assay
ChEMBL 338 11 2 2 4.3 CCCCCCCCCCC(C)(C)C(=O)N[C@@H]1CCCCNC1=O 10.1021/jm900133w
CHEMBL513863 352668 0 None 4 4 Human 9.8 pED50 = 9.8 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 2 hrs by microtiter format trans-well migration assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 2 hrs by microtiter format trans-well migration assay
ChEMBL 338 11 2 2 4.3 CCCCCCCCCCC(C)(C)C(=O)N[C@@H]1CCCCNC1=O 10.1021/jm900133w
10456104 144205 0 None 56 2 Human 10.0 pIC50 = 10 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL197375 144205 0 None 56 2 Human 10.0 pIC50 = 10 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
59278332 335613 0 None None None Human 9.7 pIC50 = 9.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 453 6 1 7 3.2 CCC(NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4457209 335613 0 None None None Human 9.7 pIC50 = 9.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 453 6 1 7 3.2 CCC(NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
59278286 336088 1 None 112 2 Human 9.7 pIC50 = 9.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 453 6 1 7 3.2 CC[C@H](NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4464625 336088 1 None 112 2 Human 9.7 pIC50 = 9.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 453 6 1 7 3.2 CC[C@H](NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
45138759 336858 0 None None None Human 9.5 pIC50 = 9.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 467 7 1 7 3.6 CCCC(NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4475581 336858 0 None None None Human 9.5 pIC50 = 9.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 467 7 1 7 3.6 CCCC(NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
512282 1562 44 None 141 4 Human 9.4 pIC50 = 9.4 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
767 1562 44 None 141 4 Human 9.4 pIC50 = 9.4 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
CHEMBL232656 1562 44 None 141 4 Human 9.4 pIC50 = 9.4 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
6918497 232475 1 None -1 4 Human 9.1 pIC50 = 9.1 Functional
Inhibitory activity against MIP-1 alpha- induced [Ca2+] response in U937 cells expressing human CCR1 receptorInhibitory activity against MIP-1 alpha- induced [Ca2+] response in U937 cells expressing human CCR1 receptor
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
CHEMBL331897 232475 1 None -1 4 Human 9.1 pIC50 = 9.1 Functional
Inhibitory activity against MIP-1 alpha- induced [Ca2+] response in U937 cells expressing human CCR1 receptorInhibitory activity against MIP-1 alpha- induced [Ca2+] response in U937 cells expressing human CCR1 receptor
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
66686405 346689 0 None None None Human 9.1 pIC50 = 9.1 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 532 5 2 5 6.3 CC(C)(O)c1ccc2c(c1)/C(=C\CCN1CC[C@](O)(c3ccc(Cl)cc3)C(C)(C)C1)c1cccnc1CO2 10.1016/j.bmcl.2018.11.015
CHEMBL4571977 346689 0 None None None Human 9.1 pIC50 = 9.1 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 532 5 2 5 6.3 CC(C)(O)c1ccc2c(c1)/C(=C\CCN1CC[C@](O)(c3ccc(Cl)cc3)C(C)(C)C1)c1cccnc1CO2 10.1016/j.bmcl.2018.11.015
9980155 144042 0 None 23 2 Human 9.1 pIC50 = 9.1 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 430 5 2 3 3.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1NC(N)=O 10.1016/j.bmcl.2005.08.057
CHEMBL196860 144042 0 None 23 2 Human 9.1 pIC50 = 9.1 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 430 5 2 3 3.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1NC(N)=O 10.1016/j.bmcl.2005.08.057
10003548 144195 0 None 223 2 Human 9.0 pIC50 = 9 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@@H](C)N(Cc2ccc(F)cc2)C[C@@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL197345 144195 0 None 223 2 Human 9.0 pIC50 = 9 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@@H](C)N(Cc2ccc(F)cc2)C[C@@H]1C 10.1016/j.bmcl.2005.08.057
11743399 144696 8 None 32 2 Human 9.0 pIC50 = 9 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 429 5 1 3 4.2 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL198949 144696 8 None 32 2 Human 9.0 pIC50 = 9 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 429 5 1 3 4.2 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
44405176 272843 0 None 1 2 Human 9.0 pIC50 = 9 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 471 6 1 4 4.3 COc1cc(/C=C/C(=O)N2C3CCC2CN(Cc2ccc(F)cc2)C3)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
CHEMBL372807 272843 0 None 1 2 Human 9.0 pIC50 = 9 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 471 6 1 4 4.3 COc1cc(/C=C/C(=O)N2C3CCC2CN(Cc2ccc(F)cc2)C3)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
44309143 468504 0 None None None Human 9.0 pIC50 = 9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 481 11 4 6 2.9 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)NN 10.1016/j.bmcl.2004.02.022
CHEMBL66159 468504 0 None None None Human 9.0 pIC50 = 9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 481 11 4 6 2.9 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)NN 10.1016/j.bmcl.2004.02.022
59278147 347111 0 None None None Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 492 5 1 6 3.9 CS(=O)(=O)c1cc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)cc(C(F)(F)F)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4518015 347111 0 None None None Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 492 5 1 6 3.9 CS(=O)(=O)c1cc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)cc(C(F)(F)F)c1 10.1016/j.bmcl.2018.12.024
512282 1562 44 None 141 4 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2018.11.015
767 1562 44 None 141 4 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2018.11.015
CHEMBL232656 1562 44 None 141 4 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2018.11.015
59278115 348867 0 None None None Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 439 5 1 7 2.8 CC(NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4562738 348867 0 None None None Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 439 5 1 7 2.8 CC(NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
512282 1562 44 None 141 4 Human 8.8 pIC50 = 8.8 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm801416q
767 1562 44 None 141 4 Human 8.8 pIC50 = 8.8 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm801416q
CHEMBL232656 1562 44 None 141 4 Human 8.8 pIC50 = 8.8 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm801416q
10434371 145166 0 None 5 2 Human 8.8 pIC50 = 8.8 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 459 6 1 4 4.2 COc1cc(/C=C/C(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
CHEMBL200629 145166 0 None 5 2 Human 8.8 pIC50 = 8.8 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 459 6 1 4 4.2 COc1cc(/C=C/C(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
52916803 335526 28 None None None Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.1016/j.bmcl.2018.12.024
CHEMBL4456123 335526 28 None None None Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.1016/j.bmcl.2018.12.024
155511620 334156 0 None None None Human 8.0 pIC50 = 8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 453 6 1 3 6.3 CCC[C@H](NC(=O)c1cnn(-c2ccc(Cl)cc2)c1C)c1cccc(C(F)(F)F)c1F 10.1016/j.bmcl.2018.11.015
CHEMBL4436061 334156 0 None None None Human 8.0 pIC50 = 8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 453 6 1 3 6.3 CCC[C@H](NC(=O)c1cnn(-c2ccc(Cl)cc2)c1C)c1cccc(C(F)(F)F)c1F 10.1016/j.bmcl.2018.11.015
11554849 145064 0 None 2 2 Human 8.0 pIC50 = 8 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 484 7 1 4 3.9 CN(C)CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
CHEMBL200242 145064 0 None 2 2 Human 8.0 pIC50 = 8 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 484 7 1 4 3.9 CN(C)CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
44453265 195757 0 None None None Human 7.0 pIC50 = 7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 442 7 2 4 3.6 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(Cl)c1 10.1016/j.bmcl.2007.09.068
CHEMBL256821 195757 0 None None None Human 7.0 pIC50 = 7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 442 7 2 4 3.6 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(Cl)c1 10.1016/j.bmcl.2007.09.068
44453400 195899 0 None None None Human 7.0 pIC50 = 7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 460 7 2 4 3.8 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(F)cc1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL257509 195899 0 None None None Human 7.0 pIC50 = 7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 460 7 2 4 3.8 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(F)cc1Cl 10.1016/j.bmcl.2007.09.068
10003548 144195 0 None 223 2 Human 7.0 pIC50 = 7 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@@H](C)N(Cc2ccc(F)cc2)C[C@@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL197345 144195 0 None 223 2 Human 7.0 pIC50 = 7 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@@H](C)N(Cc2ccc(F)cc2)C[C@@H]1C 10.1016/j.bmcl.2005.08.057
10072252 144831 0 None -17 2 Mouse 6.0 pIC50 = 6 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 446 5 1 4 4.1 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL199412 144831 0 None -17 2 Mouse 6.0 pIC50 = 6 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 446 5 1 4 4.1 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
44405203 144699 0 None 31 2 Human 6.0 pIC50 = 6 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 443 4 1 4 4.5 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)oc12 10.1016/j.bmcl.2005.08.057
CHEMBL198966 144699 0 None 31 2 Human 6.0 pIC50 = 6 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 443 4 1 4 4.5 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)oc12 10.1016/j.bmcl.2005.08.057
44405202 145203 0 None 17 2 Human 6.0 pIC50 = 6 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 442 4 2 3 4.3 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)[nH]c12 10.1016/j.bmcl.2005.08.057
CHEMBL200794 145203 0 None 17 2 Human 6.0 pIC50 = 6 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 442 4 2 3 4.3 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)[nH]c12 10.1016/j.bmcl.2005.08.057
76322249 215859 0 None None None Human 5.0 pIC50 = 5 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 880 16 6 6 11.0 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(O)c(C(=O)NCC(=O)O)c5)c5cc(Cl)c(O)c(C(=O)NCC(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
CHEMBL3137848 215859 0 None None None Human 5.0 pIC50 = 5 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 880 16 6 6 11.0 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(O)c(C(=O)NCC(=O)O)c5)c5cc(Cl)c(O)c(C(=O)NCC(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
CHEMBL3138130 477896 0 None None None Human 5.0 pIC50 = 5 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 1034 20 4 6 15.9 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(OCc6cccc(C(=O)O)c6)c(C(=O)O)c5)c5cc(Cl)c(OCc6cccc(C(=O)O)c6)c(C(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
CHEMBL3138370 477896 0 None None None Human 5.0 pIC50 = 5 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 1034 20 4 6 15.9 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(OCc6cccc(C(=O)O)c6)c(C(=O)O)c5)c5cc(Cl)c(OCc6cccc(C(=O)O)c6)c(C(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
44453225 196100 0 None None None Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 440 4 1 5 3.5 O=S(=O)(c1cccs1)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL258368 196100 0 None None None Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 440 4 1 5 3.5 O=S(=O)(c1cccs1)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
10003548 144195 0 None 223 2 Human 5.0 pIC50 = 5.0 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@@H](C)N(Cc2ccc(F)cc2)C[C@@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL197345 144195 0 None 223 2 Human 5.0 pIC50 = 5.0 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@@H](C)N(Cc2ccc(F)cc2)C[C@@H]1C 10.1016/j.bmcl.2005.08.057
10789018 78655 0 None None None Human 5.0 pIC50 = 5.0 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 435 7 1 4 5.1 N#Cc1ccc(C2(O)CCN(CCCC(C#N)(c3ccccc3)c3ccccc3)CC2)cc1 10.1021/jm990316l
CHEMBL143499 78655 0 None None None Human 5.0 pIC50 = 5.0 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 435 7 1 4 5.1 N#Cc1ccc(C2(O)CCN(CCCC(C#N)(c3ccccc3)c3ccccc3)CC2)cc1 10.1021/jm990316l
44453503 195455 0 None None None Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 490 8 2 5 4.7 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1-c1ccsc1 10.1016/j.bmcl.2007.09.068
CHEMBL255338 195455 0 None None None Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 490 8 2 5 4.7 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1-c1ccsc1 10.1016/j.bmcl.2007.09.068
58138765 348466 0 None None None Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 413 4 1 3 5.1 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1cccc(F)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4552741 348466 0 None None None Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 413 4 1 3 5.1 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1cccc(F)c1 10.1016/j.bmcl.2018.12.024
44309194 468546 0 None None None Human 5.9 pIC50 = 5.9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 464 11 4 6 2.4 CC(C)(O)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
CHEMBL66457 468546 0 None None None Human 5.9 pIC50 = 5.9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 464 11 4 6 2.4 CC(C)(O)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
44430752 178860 0 None 147 2 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 599 11 2 9 2.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCOCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL234295 178860 0 None 147 2 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 599 11 2 9 2.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCOCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44430752 178860 0 None 147 2 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 599 11 2 9 2.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCOCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL234295 178860 0 None 147 2 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 599 11 2 9 2.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCOCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
59278305 334593 0 None None None Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 424 5 1 6 2.9 CS(=O)(=O)c1ccc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4442765 334593 0 None None None Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 424 5 1 6 2.9 CS(=O)(=O)c1ccc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)cc1 10.1016/j.bmcl.2018.12.024
59278307 336084 0 None None None Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 453 5 1 7 3.0 CC(C)(NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4464575 336084 0 None None None Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 453 5 1 7 3.0 CC(C)(NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
44470374 349853 0 None None None Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 507 6 1 6 3.0 CN1CCN(S(=O)(=O)c2ccc(CNC(=O)c3cccc4c3cnn4-c3ccc(F)cc3)cc2)CC1 10.1016/j.bmcl.2018.12.024
CHEMBL4586189 349853 0 None None None Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 507 6 1 6 3.0 CN1CCN(S(=O)(=O)c2ccc(CNC(=O)c3cccc4c3cnn4-c3ccc(F)cc3)cc2)CC1 10.1016/j.bmcl.2018.12.024
44453162 195643 0 None None None Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 526 4 1 4 4.6 CC1CC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN1S(=O)(=O)c1ccccc1Br 10.1016/j.bmcl.2007.09.068
CHEMBL256272 195643 0 None None None Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 526 4 1 4 4.6 CC1CC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN1S(=O)(=O)c1ccccc1Br 10.1016/j.bmcl.2007.09.068
44453199 196031 0 None None None Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 422 7 2 4 3.3 Cc1ccc(S(=O)(=O)NCCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL258064 196031 0 None None None Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 422 7 2 4 3.3 Cc1ccc(S(=O)(=O)NCCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1 10.1016/j.bmcl.2007.09.068
44469804 336545 0 None None None Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 424 5 1 6 2.9 CS(=O)(=O)c1ccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)cn1 10.1016/j.bmcl.2018.12.024
CHEMBL4471579 336545 0 None None None Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 424 5 1 6 2.9 CS(=O)(=O)c1ccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)cn1 10.1016/j.bmcl.2018.12.024
44405203 144699 0 None 31 2 Human 6.9 pIC50 = 6.9 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 443 4 1 4 4.5 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)oc12 10.1016/j.bmcl.2005.08.057
CHEMBL198966 144699 0 None 31 2 Human 6.9 pIC50 = 6.9 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 443 4 1 4 4.5 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)oc12 10.1016/j.bmcl.2005.08.057
44309407 203014 0 None None None Human 6.9 pIC50 = 6.9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 476 9 4 6 2.5 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1(O)CCCCC1 10.1016/j.bmcl.2004.02.022
CHEMBL306457 203014 0 None None None Human 6.9 pIC50 = 6.9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 476 9 4 6 2.5 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1(O)CCCCC1 10.1016/j.bmcl.2004.02.022
44468442 335102 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 413 4 1 3 5.1 O=C(NCc1ccccc1C(F)(F)F)c1cccc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4450029 335102 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 413 4 1 3 5.1 O=C(NCc1ccccc1C(F)(F)F)c1cccc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
155530458 336072 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 409 5 2 4 4.0 O=C(NCc1cccc(C(F)(F)F)c1)c1cnn(-c2ccc(Cl)cc2)c1CO 10.1016/j.bmcl.2018.11.015
CHEMBL4464403 336072 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 409 5 2 4 4.0 O=C(NCc1cccc(C(F)(F)F)c1)c1cnn(-c2ccc(Cl)cc2)c1CO 10.1016/j.bmcl.2018.11.015
44468440 347455 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 346 4 1 4 3.5 O=C(NCc1ccncc1)c1cccc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4527255 347455 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 346 4 1 4 3.5 O=C(NCc1ccncc1)c1cccc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4647642 478360 0 None None None Human 5.9 pIC50 = 5.9 Functional
CCR1 cellular Ca2+-flux assayCCR1 cellular Ca2+-flux assay
ChEMBL 475 4 1 5 3.0 O=C([C@H]1C[C@H](O)CN1c1ccc(Cl)cc1)N1CC2COCC(C1)N2Cc1ccc(Cl)cc1 10.6019/CHEMBL4630906
44453357 197826 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 434 4 1 4 3.5 O=S(=O)(c1ccccc1)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL270419 197826 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 434 4 1 4 3.5 O=S(=O)(c1ccccc1)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44453525 197806 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 452 4 1 4 3.6 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(F)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL270358 197806 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 452 4 1 4 3.6 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(F)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44309161 468792 0 None None None Human 4.9 pIC50 = 4.9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 462 9 3 6 2.3 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCOCC1 10.1016/j.bmcl.2004.02.022
44309166 468792 0 None None None Human 4.9 pIC50 = 4.9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 462 9 3 6 2.3 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCOCC1 10.1016/j.bmcl.2004.02.022
CHEMBL68368 468792 0 None None None Human 4.9 pIC50 = 4.9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 462 9 3 6 2.3 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCOCC1 10.1016/j.bmcl.2004.02.022
CHEMBL69876 468792 0 None None None Human 4.9 pIC50 = 4.9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 462 9 3 6 2.3 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCOCC1 10.1016/j.bmcl.2004.02.022
CHEMBL3138123 477894 0 None None None Human 4.9 pIC50 = 4.9 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 1028 22 6 8 13.2 CSCC[C@H](NC(=O)c1cc(C(=CCC[C@H]2CC[C@@]3(C)C(CC[C@@H]4[C@@H]3CC[C@@]3(C)[C@H]4CC[C@@H]3C(C)CCCC(C)C)C2)c2cc(Cl)c(O)c(C(=O)N[C@@H](CCSC)C(=O)O)c2)cc(Cl)c1O)C(=O)O 10.1016/s0960-894x(00)00601-6
44453638 327635 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC[C@@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
CHEMBL427834 327635 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC[C@@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
44430746 177992 0 None 41 2 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 530 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCO)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232638 177992 0 None 41 2 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 530 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCO)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
155564974 349474 0 None None None Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 439 5 1 3 5.9 CC[C@H](NC(=O)c1cnn(-c2ccc(Cl)cc2)c1C)c1cccc(C(F)(F)F)c1F 10.1016/j.bmcl.2018.11.015
CHEMBL4577357 349474 0 None None None Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 439 5 1 3 5.9 CC[C@H](NC(=O)c1cnn(-c2ccc(Cl)cc2)c1C)c1cccc(C(F)(F)F)c1F 10.1016/j.bmcl.2018.11.015
10388824 270926 0 None 4 2 Human 7.9 pIC50 = 7.9 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 445 5 1 3 4.7 CC(=O)Nc1cc2ccccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL370596 270926 0 None 4 2 Human 7.9 pIC50 = 7.9 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 445 5 1 3 4.7 CC(=O)Nc1cc2ccccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
44309397 468791 0 None None None Human 7.9 pIC50 = 7.9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 466 11 3 5 3.4 CC(C)(F)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
CHEMBL68366 468791 0 None None None Human 7.9 pIC50 = 7.9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 466 11 3 5 3.4 CC(C)(F)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
44453320 197794 0 None None None Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL270253 197794 0 None None None Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44453579 311536 0 None None None Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 482 4 1 4 4.5 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL404465 311536 0 None None None Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 482 4 1 4 4.5 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44309364 468890 0 None None None Human 6.9 pIC50 = 6.9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 494 12 3 5 4.0 CCNC(=O)C(CCC(C)(C)F)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.022
CHEMBL69123 468890 0 None None None Human 6.9 pIC50 = 6.9 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 494 12 3 5 4.0 CCNC(=O)C(CCC(C)(C)F)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.022
44453615 195538 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Br)N1CCC[C@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
CHEMBL255797 195538 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Br)N1CCC[C@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
44453402 195937 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cc(Cl)cc(Cl)c1 10.1016/j.bmcl.2007.09.068
CHEMBL257698 195937 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cc(Cl)cc(Cl)c1 10.1016/j.bmcl.2007.09.068
10456104 144205 0 None 56 2 Human 5.9 pIC50 = 5.9 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL197375 144205 0 None 56 2 Human 5.9 pIC50 = 5.9 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
44430723 177717 0 None None None Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 544 8 2 7 3.1 CNc1c(Nc2cc(Br)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232253 177717 0 None None None Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 544 8 2 7 3.1 CNc1c(Nc2cc(Br)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453614 308735 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Br)N1CCC[C@@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
CHEMBL402825 308735 0 None None None Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Br)N1CCC[C@@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
24758044 164277 0 None 5 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced calcium flux by FLIPRAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced calcium flux by FLIPR
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57888953 164277 0 None 5 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced calcium flux by FLIPRAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced calcium flux by FLIPR
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
71455572 164277 0 None 5 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced calcium flux by FLIPRAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced calcium flux by FLIPR
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180523 164277 0 None 5 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced calcium flux by FLIPRAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced calcium flux by FLIPR
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180528 164277 0 None 5 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced calcium flux by FLIPRAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced calcium flux by FLIPR
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180534 164277 0 None 5 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced calcium flux by FLIPRAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced calcium flux by FLIPR
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44480600 349086 1 None None None Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 446 7 1 6 3.9 CCCC(NC(=O)c1cnn(-c2ccc(Cl)cc2)c1C)c1cncc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.11.015
CHEMBL4568048 349086 1 None None None Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 446 7 1 6 3.9 CCCC(NC(=O)c1cnn(-c2ccc(Cl)cc2)c1C)c1cncc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.11.015
44405212 145177 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 458 5 1 4 4.2 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
CHEMBL200680 145177 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 458 5 1 4 4.2 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
10001921 144665 0 None 3 2 Human 6.8 pIC50 = 6.8 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 415 5 1 3 3.8 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)CC1 10.1016/j.bmcl.2005.08.057
CHEMBL198852 144665 0 None 3 2 Human 6.8 pIC50 = 6.8 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 415 5 1 3 3.8 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)CC1 10.1016/j.bmcl.2005.08.057
512282 1562 44 None -141 4 Mouse 5.8 pIC50 = 5.8 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
767 1562 44 None -141 4 Mouse 5.8 pIC50 = 5.8 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
CHEMBL232656 1562 44 None -141 4 Mouse 5.8 pIC50 = 5.8 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
10388824 270926 0 None 4 2 Human 5.8 pIC50 = 5.8 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 445 5 1 3 4.7 CC(=O)Nc1cc2ccccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL370596 270926 0 None 4 2 Human 5.8 pIC50 = 5.8 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 445 5 1 3 4.7 CC(=O)Nc1cc2ccccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
49865900 40073 0 None None None Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrsAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrs
ChEMBL 448 4 1 3 6.0 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCCC1c1nccn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
CHEMBL1224118 40073 0 None None None Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrsAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrs
ChEMBL 448 4 1 3 6.0 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCCC1c1nccn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
24782574 353253 0 None None None Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 453 4 1 2 5.3 Cc1cc(C(F)(F)F)ccc1NC(=O)N1CCC[C@@H]1C(=O)N(C)Cc1ccc(Cl)cc1 10.1021/jm801416q
CHEMBL473734 353253 0 None None None Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 453 4 1 2 5.3 Cc1cc(C(F)(F)F)ccc1NC(=O)N1CCC[C@@H]1C(=O)N(C)Cc1ccc(Cl)cc1 10.1021/jm801416q
9980155 144042 0 None 23 2 Human 7.8 pIC50 = 7.8 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 430 5 2 3 3.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1NC(N)=O 10.1016/j.bmcl.2005.08.057
CHEMBL196860 144042 0 None 23 2 Human 7.8 pIC50 = 7.8 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 430 5 2 3 3.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1NC(N)=O 10.1016/j.bmcl.2005.08.057
44405234 270765 0 None None None Human 5.8 pIC50 = 5.8 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL370447 270765 0 None None None Human 5.8 pIC50 = 5.8 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
10575889 67305 0 None None None Human 5.8 pIC50 = 5.8 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 458 8 1 3 6.3 N#CC(CCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL142199 67305 0 None None None Human 5.8 pIC50 = 5.8 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 458 8 1 3 6.3 N#CC(CCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
44453084 195641 0 None None None Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 422 6 2 3 4.6 O=C(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc2ccccc2c1 10.1016/j.bmcl.2007.09.068
CHEMBL256264 195641 0 None None None Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 422 6 2 3 4.6 O=C(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc2ccccc2c1 10.1016/j.bmcl.2007.09.068
44430713 177592 0 None 30 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 500 8 2 7 3.0 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL231829 177592 0 None 30 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 500 8 2 7 3.0 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
58138868 335099 0 None None None Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 414 4 1 4 4.5 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1ccc(F)nc1 10.1016/j.bmcl.2018.12.024
CHEMBL4449996 335099 0 None None None Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 414 4 1 4 4.5 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1ccc(F)nc1 10.1016/j.bmcl.2018.12.024
58138852 348131 0 None None None Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 452 7 2 5 3.4 CCNS(=O)(=O)c1cccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4544186 348131 0 None None None Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 452 7 2 5 3.4 CCNS(=O)(=O)c1cccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
58138832 334441 0 None None None Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 403 5 1 5 3.9 COC(=O)c1cccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4440452 334441 0 None None None Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 403 5 1 5 3.9 COC(=O)c1cccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
155544726 348970 0 None None None Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 403 5 1 5 3.2 Cc1c(C(=O)NCc2ccc(S(C)(=O)=O)cc2)cnn1-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.11.015
CHEMBL4565390 348970 0 None None None Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 403 5 1 5 3.2 Cc1c(C(=O)NCc2ccc(S(C)(=O)=O)cc2)cnn1-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.11.015
44405194 144059 0 None None None Human 5.8 pIC50 = 5.8 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 427 5 1 3 3.9 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@H]2C[C@@H]1CN2Cc1ccc(F)cc1 10.1016/j.bmcl.2005.08.057
CHEMBL196908 144059 0 None None None Human 5.8 pIC50 = 5.8 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 427 5 1 3 3.9 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@H]2C[C@@H]1CN2Cc1ccc(F)cc1 10.1016/j.bmcl.2005.08.057
44405181 260685 0 None 51 2 Human 5.8 pIC50 = 5.8 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 432 6 2 4 3.6 CC(=O)Nc1cc(Cl)ccc1NCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL370162 260685 0 None 51 2 Human 5.8 pIC50 = 5.8 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 432 6 2 4 3.6 CC(=O)Nc1cc(Cl)ccc1NCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
512282 1562 44 None 141 4 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2007.03.104
767 1562 44 None 141 4 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2007.03.104
CHEMBL232656 1562 44 None 141 4 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2007.03.104
512282 1562 44 None 141 4 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2007.03.104
767 1562 44 None 141 4 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2007.03.104
CHEMBL232656 1562 44 None 141 4 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2007.03.104
44430713 177592 0 None 30 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 500 8 2 7 3.0 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL231829 177592 0 None 30 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 500 8 2 7 3.0 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453467 196094 0 None None None Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 502 4 1 4 4.8 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)c(Cl)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL258359 196094 0 None None None Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 502 4 1 4 4.8 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)c(Cl)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44453363 197829 0 None None None Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 458 7 2 4 4.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc2ccccc12 10.1016/j.bmcl.2007.09.068
CHEMBL270433 197829 0 None None None Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 458 7 2 4 4.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc2ccccc12 10.1016/j.bmcl.2007.09.068
44453501 198109 0 None None None Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Br)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL271903 198109 0 None None None Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Br)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44453292 311437 0 None None None Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 448 4 1 4 3.8 Cc1ccccc1S(=O)(=O)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL404033 311437 0 None None None Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 448 4 1 4 3.8 Cc1ccccc1S(=O)(=O)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
58138893 349481 0 None None None Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 466 7 2 5 3.8 CC(C)NS(=O)(=O)c1cccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4577460 349481 0 None None None Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 466 7 2 5 3.8 CC(C)NS(=O)(=O)c1cccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
11801020 26518 0 None None None Human 5.8 pIC50 = 5.8 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 434 7 1 1 6.4 C[N+]1(CCCC(c2ccccc2)c2ccccc2)CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
CHEMBL1184558 26518 0 None None None Human 5.8 pIC50 = 5.8 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 434 7 1 1 6.4 C[N+]1(CCCC(c2ccccc2)c2ccccc2)CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
22725647 347783 0 None -52 2 Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 347 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)c(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4535696 347783 0 None -52 2 Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 347 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)c(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
44430745 279221 0 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 544 11 2 8 3.0 COCCNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL387822 279221 0 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 544 11 2 8 3.0 COCCNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
45138458 336220 0 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 439 6 1 7 2.7 CCS(=O)(=O)c1cc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)ccn1 10.1016/j.bmcl.2018.12.024
CHEMBL4466500 336220 0 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 439 6 1 7 2.7 CCS(=O)(=O)c1cc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)ccn1 10.1016/j.bmcl.2018.12.024
44453164 196096 0 None None None Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 492 8 2 5 3.9 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1OC(F)(F)F 10.1016/j.bmcl.2007.09.068
CHEMBL258361 196096 0 None None None Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 492 8 2 5 3.9 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1OC(F)(F)F 10.1016/j.bmcl.2007.09.068
10001921 144665 0 None 3 2 Human 6.7 pIC50 = 6.7 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 415 5 1 3 3.8 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)CC1 10.1016/j.bmcl.2005.08.057
CHEMBL198852 144665 0 None 3 2 Human 6.7 pIC50 = 6.7 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 415 5 1 3 3.8 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)CC1 10.1016/j.bmcl.2005.08.057
155533145 336351 0 None None None Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 409 4 1 2 6.3 Cc1cc(-c2ccc(Cl)cc2)sc1C(=O)NCc1cccc(C(F)(F)F)c1 10.1016/j.bmcl.2018.11.015
CHEMBL4468514 336351 0 None None None Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 409 4 1 2 6.3 Cc1cc(-c2ccc(Cl)cc2)sc1C(=O)NCc1cccc(C(F)(F)F)c1 10.1016/j.bmcl.2018.11.015
10766998 77515 0 None None None Human 5.7 pIC50 = 5.7 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 476 7 1 4 5.5 COc1ccc(C(C#N)CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1Br 10.1021/jm990316l
CHEMBL142468 77515 0 None None None Human 5.7 pIC50 = 5.7 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 476 7 1 4 5.5 COc1ccc(C(C#N)CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1Br 10.1021/jm990316l
22725647 347783 0 None -52 2 Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 347 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)c(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4535696 347783 0 None -52 2 Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 347 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)c(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
10164 1805 30 None None None Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 451 4 1 8 2.2 COc1cc(ccc1Cl)N1CCN(CC1)C(=O)Cn1[nH]c(=C2N=CC=N2)c2c1nccc2 10.1016/j.bmcl.2018.11.015
135565361 1805 30 None None None Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 451 4 1 8 2.2 COc1cc(ccc1Cl)N1CCN(CC1)C(=O)Cn1[nH]c(=C2N=CC=N2)c2c1nccc2 10.1016/j.bmcl.2018.11.015
25016615 1805 30 None None None Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 451 4 1 8 2.2 COc1cc(ccc1Cl)N1CCN(CC1)C(=O)Cn1[nH]c(=C2N=CC=N2)c2c1nccc2 10.1016/j.bmcl.2018.11.015
CHEMBL4444976 1805 30 None None None Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 451 4 1 8 2.2 COc1cc(ccc1Cl)N1CCN(CC1)C(=O)Cn1[nH]c(=C2N=CC=N2)c2c1nccc2 10.1016/j.bmcl.2018.11.015
DB12963 1805 30 None None None Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 451 4 1 8 2.2 COc1cc(ccc1Cl)N1CCN(CC1)C(=O)Cn1[nH]c(=C2N=CC=N2)c2c1nccc2 10.1016/j.bmcl.2018.11.015
52917500 336792 0 None None None Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 465 5 1 7 3.2 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CCC2)ccn1 10.1016/j.bmcl.2018.12.024
CHEMBL4474606 336792 0 None None None Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 465 5 1 7 3.2 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CCC2)ccn1 10.1016/j.bmcl.2018.12.024
59278436 336829 0 None None None Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 439 6 2 6 2.4 CNS(=O)(=O)c1ccc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4475173 336829 0 None None None Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 439 6 2 6 2.4 CNS(=O)(=O)c1ccc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)cc1 10.1016/j.bmcl.2018.12.024
10049340 202703 0 None None None Human 8.7 pIC50 = 8.7 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 448 11 3 5 3.3 CC(C)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
CHEMBL304358 202703 0 None None None Human 8.7 pIC50 = 8.7 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 448 11 3 5 3.3 CC(C)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
512282 1562 44 None 141 4 Human 8.6 pIC50 = 8.6 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
767 1562 44 None 141 4 Human 8.6 pIC50 = 8.6 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
CHEMBL232656 1562 44 None 141 4 Human 8.6 pIC50 = 8.6 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
44405181 260685 0 None 51 2 Human 8.6 pIC50 = 8.6 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 432 6 2 4 3.6 CC(=O)Nc1cc(Cl)ccc1NCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL370162 260685 0 None 51 2 Human 8.6 pIC50 = 8.6 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 432 6 2 4 3.6 CC(=O)Nc1cc(Cl)ccc1NCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
49865951 40089 0 None None None Human 8.5 pIC50 = 8.5 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrsAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrs
ChEMBL 463 4 1 4 5.7 Cc1nnc([C@H]2CCCN2C(=O)Nc2ccc(C(F)(F)F)cc2)n1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
CHEMBL1224189 40089 0 None None None Human 8.5 pIC50 = 8.5 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrsAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrs
ChEMBL 463 4 1 4 5.7 Cc1nnc([C@H]2CCCN2C(=O)Nc2ccc(C(F)(F)F)cc2)n1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
10072252 144831 0 None 17 2 Human 7.7 pIC50 = 7.7 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 446 5 1 4 4.1 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL199412 144831 0 None 17 2 Human 7.7 pIC50 = 7.7 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 446 5 1 4 4.1 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
10434371 145166 0 None 5 2 Human 7.7 pIC50 = 7.7 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 459 6 1 4 4.2 COc1cc(/C=C/C(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
CHEMBL200629 145166 0 None 5 2 Human 7.7 pIC50 = 7.7 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 459 6 1 4 4.2 COc1cc(/C=C/C(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
11719164 277557 0 None None None Human 6.7 pIC50 = 6.7 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 441 5 1 3 4.3 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
CHEMBL380568 277557 0 None None None Human 6.7 pIC50 = 6.7 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 441 5 1 3 4.3 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
44453637 198288 0 None None None Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC[C@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
CHEMBL272758 198288 0 None None None Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC[C@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
6918497 232475 1 None -17 4 Mouse 7.7 pIC50 = 7.7 Functional
inhibitory activity against MIP-1 alpha- induced [Ca2+] response in U937 cells expressing mouse CCR1 receptorinhibitory activity against MIP-1 alpha- induced [Ca2+] response in U937 cells expressing mouse CCR1 receptor
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
CHEMBL331897 232475 1 None -17 4 Mouse 7.7 pIC50 = 7.7 Functional
inhibitory activity against MIP-1 alpha- induced [Ca2+] response in U937 cells expressing mouse CCR1 receptorinhibitory activity against MIP-1 alpha- induced [Ca2+] response in U937 cells expressing mouse CCR1 receptor
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
44453229 195770 0 None None None Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 426 7 2 4 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(F)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL256889 195770 0 None None None Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 426 7 2 4 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(F)cc1 10.1016/j.bmcl.2007.09.068
58138845 350091 0 None None None Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 429 4 1 3 5.6 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4591935 350091 0 None None None Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 429 4 1 3 5.6 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.12.024
155562877 349241 0 None None None Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 403 5 1 5 3.2 Cc1c(C(=O)NCc2cccc(S(C)(=O)=O)c2)cnn1-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.11.015
CHEMBL4571547 349241 0 None None None Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 403 5 1 5 3.2 Cc1c(C(=O)NCc2cccc(S(C)(=O)=O)c2)cnn1-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.11.015
25254218 40075 0 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrsAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrs
ChEMBL 449 4 1 4 5.4 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCC[C@@H]1c1ncnn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
CHEMBL1224120 40075 0 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrsAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrs
ChEMBL 449 4 1 4 5.4 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCC[C@@H]1c1ncnn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
24782826 372710 4 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrsAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrs
ChEMBL 439 4 1 2 5.0 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1 10.1016/j.bmcl.2010.07.082
CHEMBL514611 372710 4 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrsAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrs
ChEMBL 439 4 1 2 5.0 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1 10.1016/j.bmcl.2010.07.082
25233755 353230 0 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 457 4 1 2 5.2 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1F 10.1021/jm801416q
CHEMBL473532 353230 0 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 457 4 1 2 5.2 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1F 10.1021/jm801416q
24782826 372710 4 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 439 4 1 2 5.0 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1 10.1021/jm801416q
CHEMBL514611 372710 4 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 439 4 1 2 5.0 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1 10.1021/jm801416q
58138826 334956 0 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 413 4 1 3 5.1 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4448064 334956 0 None None None Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 413 4 1 3 5.1 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
44309195 202240 0 None None None Human 6.7 pIC50 = 6.7 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 496 9 3 5 3.6 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCC(F)(F)CC1 10.1016/j.bmcl.2004.02.022
CHEMBL302533 202240 0 None None None Human 6.7 pIC50 = 6.7 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 496 9 3 5 3.6 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCC(F)(F)CC1 10.1016/j.bmcl.2004.02.022
44453167 196098 0 None None None Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.0 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(C(F)(F)F)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL258363 196098 0 None None None Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.0 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(C(F)(F)F)cc1 10.1016/j.bmcl.2007.09.068
44453195 311166 0 None None None Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 496 4 1 4 4.8 Cc1cccc(Cl)c1S(=O)(=O)N1CCC(C)(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL402327 311166 0 None None None Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 496 4 1 4 4.8 Cc1cccc(Cl)c1S(=O)(=O)N1CCC(C)(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44453197 311380 0 None None None Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 482 4 1 4 4.5 CC1(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN(S(=O)(=O)c2ccccc2Cl)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL403665 311380 0 None None None Human 5.7 pIC50 = 5.7 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 482 4 1 4 4.5 CC1(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN(S(=O)(=O)c2ccccc2Cl)CC1 10.1016/j.bmcl.2007.09.068
44430748 178095 0 None 72 2 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 529 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232837 178095 0 None 72 2 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 529 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453504 195893 0 None None None Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 490 8 2 5 4.7 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1-c1cccs1 10.1016/j.bmcl.2007.09.068
CHEMBL257452 195893 0 None None None Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 490 8 2 5 4.7 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1-c1cccs1 10.1016/j.bmcl.2007.09.068
10003548 144195 0 None -223 2 Mouse 4.6 pIC50 = 4.6 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@@H](C)N(Cc2ccc(F)cc2)C[C@@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL197345 144195 0 None -223 2 Mouse 4.6 pIC50 = 4.6 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@@H](C)N(Cc2ccc(F)cc2)C[C@@H]1C 10.1016/j.bmcl.2005.08.057
52916803 335526 28 None None None Human 7.6 pIC50 = 7.6 Functional
Affinity Phenotypic Cellular interaction (Functional cellular assay (measuring calcium flux in response to MIP-1a in CCR1-transfected cells)) EUB0000352a CCR1Affinity Phenotypic Cellular interaction (Functional cellular assay (measuring calcium flux in response to MIP-1a in CCR1-transfected cells)) EUB0000352a CCR1
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL5209897
CHEMBL4456123 335526 28 None None None Human 7.6 pIC50 = 7.6 Functional
Affinity Phenotypic Cellular interaction (Functional cellular assay (measuring calcium flux in response to MIP-1a in CCR1-transfected cells)) EUB0000352a CCR1Affinity Phenotypic Cellular interaction (Functional cellular assay (measuring calcium flux in response to MIP-1a in CCR1-transfected cells)) EUB0000352a CCR1
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL5209897
46858281 335946 2 None None None Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 394 4 1 4 4.2 Cc1c(C(=O)NCc2cccc(C(F)(F)F)c2)nnn1-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.11.015
CHEMBL4462565 335946 2 None None None Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 394 4 1 4 4.2 Cc1c(C(=O)NCc2cccc(C(F)(F)F)c2)nnn1-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.11.015
44453433 316434 0 None None None Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2007.09.068
CHEMBL411476 316434 0 None None None Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2007.09.068
44430723 177717 0 None None None Human 7.6 pIC50 = 7.6 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 544 8 2 7 3.1 CNc1c(Nc2cc(Br)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232253 177717 0 None None None Human 7.6 pIC50 = 7.6 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 544 8 2 7 3.1 CNc1c(Nc2cc(Br)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44469380 334803 0 None None None Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 413 4 1 3 5.1 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1ccccc1F 10.1016/j.bmcl.2018.12.024
CHEMBL4445779 334803 0 None None None Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 413 4 1 3 5.1 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1ccccc1F 10.1016/j.bmcl.2018.12.024
9889700 237386 15 None 11 4 Human 5.6 pIC50 = 5.6 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 444 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL34166 237386 15 None 11 4 Human 5.6 pIC50 = 5.6 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 444 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
44453464 195673 0 None None None Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 488 4 1 4 3.9 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3cc(F)c(F)c(F)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL256449 195673 0 None None None Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 488 4 1 4 3.9 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3cc(F)c(F)c(F)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
58138911 348658 0 None None None Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 463 4 1 3 6.3 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4557554 348658 0 None None None Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 463 4 1 3 6.3 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2018.12.024
76336764 215866 0 None None None Human 6.6 pIC50 = 6.6 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 766 12 4 4 12.8 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(O)c(C(=O)O)c5)c5cc(Cl)c(O)c(C(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
CHEMBL3138187 215866 0 None None None Human 6.6 pIC50 = 6.6 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 766 12 4 4 12.8 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(O)c(C(=O)O)c5)c5cc(Cl)c(O)c(C(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
CHEMBL3138134 477897 0 None None None Human 6.6 pIC50 = 6.6 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 1034 20 4 6 15.9 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(OCc6ccccc6C(=O)O)c(C(=O)O)c5)c5cc(Cl)c(OCc6ccccc6C(=O)O)c(C(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
CHEMBL3138376 477897 0 None None None Human 6.6 pIC50 = 6.6 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 1034 20 4 6 15.9 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(OCc6ccccc6C(=O)O)c(C(=O)O)c5)c5cc(Cl)c(OCc6ccccc6C(=O)O)c(C(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
44453157 311251 0 None None None Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 482 4 1 4 4.4 Cc1cccc(Cl)c1S(=O)(=O)N1CCC[C@@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
CHEMBL402827 311251 0 None None None Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 482 4 1 4 4.4 Cc1cccc(Cl)c1S(=O)(=O)N1CCC[C@@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
155538947 346912 0 None None None Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 425 4 1 3 5.5 Cc1c(C(=O)N[C@@H](C)c2cccc(C(F)(F)F)c2F)cnn1-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.11.015
CHEMBL4513370 346912 0 None None None Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 425 4 1 3 5.5 Cc1c(C(=O)N[C@@H](C)c2cccc(C(F)(F)F)c2F)cnn1-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.11.015
44405203 144699 0 None 31 2 Human 7.6 pIC50 = 7.6 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 443 4 1 4 4.5 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)oc12 10.1016/j.bmcl.2005.08.057
CHEMBL198966 144699 0 None 31 2 Human 7.6 pIC50 = 7.6 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 443 4 1 4 4.5 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)oc12 10.1016/j.bmcl.2005.08.057
44453161 195642 0 None None None Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 482 4 1 4 4.5 CC1CC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN1S(=O)(=O)c1ccccc1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL256271 195642 0 None None None Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 482 4 1 4 4.5 CC1CC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN1S(=O)(=O)c1ccccc1Cl 10.1016/j.bmcl.2007.09.068
44453435 197904 0 None None None Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cc(Cl)ccc1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL270863 197904 0 None None None Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cc(Cl)ccc1Cl 10.1016/j.bmcl.2007.09.068
44537841 1390 22 None 114 2 Human 8.5 pIC50 = 8.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2018.11.015
57889181 1390 22 None 114 2 Human 8.5 pIC50 = 8.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2018.11.015
9497 1390 22 None 114 2 Human 8.5 pIC50 = 8.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2018.11.015
CHEMBL2398716 1390 22 None 114 2 Human 8.5 pIC50 = 8.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2018.11.015
CHEMBL3334824 1390 22 None 114 2 Human 8.5 pIC50 = 8.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2018.11.015
45138007 335004 0 None None None Human 8.5 pIC50 = 8.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 414 4 1 4 4.5 O=C(NCc1cccc(C(F)(F)F)c1)c1cncc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4448761 335004 0 None None None Human 8.5 pIC50 = 8.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 414 4 1 4 4.5 O=C(NCc1cccc(C(F)(F)F)c1)c1cncc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4638406 478355 5 None None None Human 8.5 pIC50 = 8.5 Functional
CCR1 cellular Ca2+-flux assayCCR1 cellular Ca2+-flux assay
ChEMBL 505 5 1 6 3.4 CCOc1cc(N2C3COCC2CN(C(=O)[C@H]2C[C@H](O)CN2c2ccc(Cl)cc2)C3)ccc1Cl 10.6019/CHEMBL4630906
71462570 163992 0 None None None Human 8.5 pIC50 = 8.5 Functional
Antagonist activity at CCR1 assessed as inhibition of CCL3-induced chemotaxis by cell based assayAntagonist activity at CCR1 assessed as inhibition of CCL3-induced chemotaxis by cell based assay
ChEMBL 518 5 2 5 5.6 CC1(C)CN(CC/C=C2/c3cc(C(=O)O)ccc3OCc3ncccc32)C[C@H](c2ccc(Cl)cc2)[C@H]1O 10.1021/jm300682j
CHEMBL2178569 163992 0 None None None Human 8.5 pIC50 = 8.5 Functional
Antagonist activity at CCR1 assessed as inhibition of CCL3-induced chemotaxis by cell based assayAntagonist activity at CCR1 assessed as inhibition of CCL3-induced chemotaxis by cell based assay
ChEMBL 518 5 2 5 5.6 CC1(C)CN(CC/C=C2/c3cc(C(=O)O)ccc3OCc3ncccc32)C[C@H](c2ccc(Cl)cc2)[C@H]1O 10.1021/jm300682j
44453403 195510 0 None None None Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1c(Cl)cccc1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL255629 195510 0 None None None Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1c(Cl)cccc1Cl 10.1016/j.bmcl.2007.09.068
44453202 195665 0 None None None Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 422 7 2 4 3.3 Cc1ccccc1S(=O)(=O)NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL256404 195665 0 None None None Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 422 7 2 4 3.3 Cc1ccccc1S(=O)(=O)NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2007.09.068
11743399 144696 8 None 32 2 Human 7.5 pIC50 = 7.5 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 429 5 1 3 4.2 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL198949 144696 8 None 32 2 Human 7.5 pIC50 = 7.5 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 429 5 1 3 4.2 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
10072252 144831 0 None 17 2 Human 7.5 pIC50 = 7.5 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 446 5 1 4 4.1 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL199412 144831 0 None 17 2 Human 7.5 pIC50 = 7.5 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 446 5 1 4 4.1 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
11554849 145064 0 None 2 2 Human 7.5 pIC50 = 7.5 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 484 7 1 4 3.9 CN(C)CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
CHEMBL200242 145064 0 None 2 2 Human 7.5 pIC50 = 7.5 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 484 7 1 4 3.9 CN(C)CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
44405211 271068 0 None None None Human 6.5 pIC50 = 6.5 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 441 5 1 3 4.3 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CC2CCC(C1)N2Cc1ccc(F)cc1 10.1016/j.bmcl.2005.08.057
CHEMBL371248 271068 0 None None None Human 6.5 pIC50 = 6.5 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 441 5 1 3 4.3 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CC2CCC(C1)N2Cc1ccc(F)cc1 10.1016/j.bmcl.2005.08.057
9980155 144042 0 None -23 2 Mouse 6.5 pIC50 = 6.5 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 430 5 2 3 3.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1NC(N)=O 10.1016/j.bmcl.2005.08.057
CHEMBL196860 144042 0 None -23 2 Mouse 6.5 pIC50 = 6.5 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 430 5 2 3 3.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1NC(N)=O 10.1016/j.bmcl.2005.08.057
10072252 144831 0 None 17 2 Human 6.5 pIC50 = 6.5 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 446 5 1 4 4.1 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL199412 144831 0 None 17 2 Human 6.5 pIC50 = 6.5 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 446 5 1 4 4.1 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
44405202 145203 0 None -17 2 Mouse 5.5 pIC50 = 5.5 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 442 4 2 3 4.3 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)[nH]c12 10.1016/j.bmcl.2005.08.057
CHEMBL200794 145203 0 None -17 2 Mouse 5.5 pIC50 = 5.5 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 442 4 2 3 4.3 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)[nH]c12 10.1016/j.bmcl.2005.08.057
44405181 260685 0 None -51 2 Mouse 5.5 pIC50 = 5.5 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 432 6 2 4 3.6 CC(=O)Nc1cc(Cl)ccc1NCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL370162 260685 0 None -51 2 Mouse 5.5 pIC50 = 5.5 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 432 6 2 4 3.6 CC(=O)Nc1cc(Cl)ccc1NCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
9804868 67454 1 None None None Human 5.5 pIC50 = 5.5 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 472 5 1 4 6.0 N#CC1(CCCN2CCC(O)(c3ccc(F)cc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
CHEMBL142318 67454 1 None None None Human 5.5 pIC50 = 5.5 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 472 5 1 4 6.0 N#CC1(CCCN2CCC(O)(c3ccc(F)cc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
44309122 202876 0 None None None Human 7.5 pIC50 = 7.5 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 482 11 4 6 3.4 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)NO 10.1016/j.bmcl.2004.02.022
CHEMBL305423 202876 0 None None None Human 7.5 pIC50 = 7.5 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 482 11 4 6 3.4 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)NO 10.1016/j.bmcl.2004.02.022
1370410 177778 10 None None None Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced calcium flux by FLIPR assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced calcium flux by FLIPR assay
ChEMBL 404 3 0 4 3.4 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(F)cc2)CC1 10.1016/j.bmcl.2013.01.005
CHEMBL2322888 177778 10 None None None Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced calcium flux by FLIPR assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced calcium flux by FLIPR assay
ChEMBL 404 3 0 4 3.4 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(F)cc2)CC1 10.1016/j.bmcl.2013.01.005
11743399 144696 8 None 32 2 Human 6.5 pIC50 = 6.5 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 429 5 1 3 4.2 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL198949 144696 8 None 32 2 Human 6.5 pIC50 = 6.5 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 429 5 1 3 4.2 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
10811393 78377 0 None None None Human 5.5 pIC50 = 5.5 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 407 7 1 4 4.8 N#CCC(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
CHEMBL143194 78377 0 None None None Human 5.5 pIC50 = 5.5 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 407 7 1 4 4.8 N#CCC(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
44453227 195768 0 None None None Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 548 4 1 4 4.5 O=S(=O)(c1c(F)cc(F)cc1Br)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL256887 195768 0 None None None Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 548 4 1 4 4.5 O=S(=O)(c1c(F)cc(F)cc1Br)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
10649043 78046 0 None None None Human 5.5 pIC50 = 5.5 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 499 5 1 4 5.5 CN1C(=O)c2ccccc2C(C#N)(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc21 10.1021/jm990316l
CHEMBL142925 78046 0 None None None Human 5.5 pIC50 = 5.5 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 499 5 1 4 5.5 CN1C(=O)c2ccccc2C(C#N)(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc21 10.1021/jm990316l
45138010 335404 0 None None None Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 425 5 1 7 2.3 CS(=O)(=O)c1ccc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)cn1 10.1016/j.bmcl.2018.12.024
CHEMBL4454067 335404 0 None None None Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 425 5 1 7 2.3 CS(=O)(=O)c1ccc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)cn1 10.1016/j.bmcl.2018.12.024
25233754 353229 0 None None None Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 473 4 1 2 5.7 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1Cl 10.1021/jm801416q
CHEMBL473531 353229 0 None None None Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 473 4 1 2 5.7 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1Cl 10.1021/jm801416q
44453469 196095 0 None None None Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(Cl)c1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL258360 196095 0 None None None Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(Cl)c1Cl 10.1016/j.bmcl.2007.09.068
155526212 335579 0 None None None Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 406 4 1 2 5.7 Cc1cc(C(=O)NCc2cccc(C(F)(F)F)c2)c(C)n1-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.11.015
CHEMBL4456839 335579 0 None None None Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 406 4 1 2 5.7 Cc1cc(C(=O)NCc2cccc(C(F)(F)F)c2)c(C)n1-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.11.015
44453437 316435 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)cc1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL411477 316435 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)cc1Cl 10.1016/j.bmcl.2007.09.068
44405180 277910 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 431 6 1 3 4.1 CC(=O)Nc1cc(Cl)ccc1CCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL381446 277910 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 431 6 1 3 4.1 CC(=O)Nc1cc(Cl)ccc1CCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
44453165 196097 0 None None None Human 5.4 pIC50 = 5.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 492 8 2 5 3.9 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(OC(F)(F)F)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL258362 196097 0 None None None Human 5.4 pIC50 = 5.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 492 8 2 5 3.9 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(OC(F)(F)F)cc1 10.1016/j.bmcl.2007.09.068
44453263 311580 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 442 7 2 4 3.6 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL404732 311580 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 442 7 2 4 3.6 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)cc1 10.1016/j.bmcl.2007.09.068
44430755 309540 0 None 42 2 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 577 10 2 8 3.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2cccnc2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL397910 309540 0 None 42 2 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 577 10 2 8 3.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2cccnc2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453528 197843 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 414 7 2 5 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccsc1 10.1016/j.bmcl.2007.09.068
CHEMBL270564 197843 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 414 7 2 5 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccsc1 10.1016/j.bmcl.2007.09.068
44430753 279194 0 None 77 2 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 598 11 3 9 2.2 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCNCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL387608 279194 0 None 77 2 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 598 11 3 9 2.2 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCNCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
25252974 40088 0 None None None Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrsAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrs
ChEMBL 449 4 1 4 5.4 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCC[C@@H]1c1nncn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
CHEMBL1224188 40088 0 None None None Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrsAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrs
ChEMBL 449 4 1 4 5.4 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCC[C@@H]1c1nncn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
17753030 177887 0 None 39 2 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 486 7 2 7 2.5 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(N)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232441 177887 0 None 39 2 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 486 7 2 7 2.5 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(N)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
10434371 145166 0 None 5 2 Human 8.4 pIC50 = 8.4 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 459 6 1 4 4.2 COc1cc(/C=C/C(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
CHEMBL200629 145166 0 None 5 2 Human 8.4 pIC50 = 8.4 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 459 6 1 4 4.2 COc1cc(/C=C/C(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
44405176 272843 0 None -1 2 Mouse 8.4 pIC50 = 8.4 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 471 6 1 4 4.3 COc1cc(/C=C/C(=O)N2C3CCC2CN(Cc2ccc(F)cc2)C3)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
CHEMBL372807 272843 0 None -1 2 Mouse 8.4 pIC50 = 8.4 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 471 6 1 4 4.3 COc1cc(/C=C/C(=O)N2C3CCC2CN(Cc2ccc(F)cc2)C3)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
58138789 336834 0 None None None Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 438 6 2 5 3.0 CNS(=O)(=O)c1ccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4475237 336834 0 None None None Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 438 6 2 5 3.0 CNS(=O)(=O)c1ccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)cc1 10.1016/j.bmcl.2018.12.024
21070989 177765 0 None 354 2 Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL15/Leukotactin1-induced calcium flux by FLIPR assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL15/Leukotactin1-induced calcium flux by FLIPR assay
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None 354 2 Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL15/Leukotactin1-induced calcium flux by FLIPR assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL15/Leukotactin1-induced calcium flux by FLIPR assay
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
44453291 197729 0 None None None Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 442 7 2 4 3.6 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL269957 197729 0 None None None Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 442 7 2 4 3.6 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1Cl 10.1016/j.bmcl.2007.09.068
44453361 332112 0 None None None Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 456 7 2 4 4.0 Cc1cccc(Cl)c1S(=O)(=O)NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL429419 332112 0 None None None Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 456 7 2 4 4.0 Cc1cccc(Cl)c1S(=O)(=O)NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2007.09.068
512282 1562 44 None 141 4 Human 7.4 pIC50 = 7.4 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
767 1562 44 None 141 4 Human 7.4 pIC50 = 7.4 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
CHEMBL232656 1562 44 None 141 4 Human 7.4 pIC50 = 7.4 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
11554849 145064 0 None -2 2 Mouse 7.4 pIC50 = 7.4 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 484 7 1 4 3.9 CN(C)CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
CHEMBL200242 145064 0 None -2 2 Mouse 7.4 pIC50 = 7.4 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 484 7 1 4 3.9 CN(C)CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
9980155 144042 0 None 23 2 Human 7.4 pIC50 = 7.4 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 430 5 2 3 3.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1NC(N)=O 10.1016/j.bmcl.2005.08.057
CHEMBL196860 144042 0 None 23 2 Human 7.4 pIC50 = 7.4 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 430 5 2 3 3.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1NC(N)=O 10.1016/j.bmcl.2005.08.057
9845614 239888 19 None None None Human 6.4 pIC50 = 6.4 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 430 6 1 3 5.5 N#CC(CCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL357919 239888 19 None None None Human 6.4 pIC50 = 6.4 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 430 6 1 3 5.5 N#CC(CCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL3138115 477899 0 None None None Human 5.4 pIC50 = 5.4 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 1034 20 6 8 11.9 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(OCc6cccc(B(O)O)c6)c(C(=O)O)c5)c5cc(Cl)c(OCc6cccc(B(O)O)c6)c(C(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
CHEMBL3138540 477899 0 None None None Human 5.4 pIC50 = 5.4 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 1034 20 6 8 11.9 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(OCc6cccc(B(O)O)c6)c(C(=O)O)c5)c5cc(Cl)c(OCc6cccc(B(O)O)c6)c(C(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
59278474 336657 0 None None None Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 451 6 1 7 2.8 O=C(NCc1ccnc(S(=O)(=O)C2CC2)c1)c1cncc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4472994 336657 0 None None None Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 451 6 1 7 2.8 O=C(NCc1ccnc(S(=O)(=O)C2CC2)c1)c1cncc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
11554849 145064 0 None 2 2 Human 7.4 pIC50 = 7.4 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 484 7 1 4 3.9 CN(C)CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
CHEMBL200242 145064 0 None 2 2 Human 7.4 pIC50 = 7.4 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 484 7 1 4 3.9 CN(C)CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
44453321 197795 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 502 4 1 4 4.8 O=S(=O)(c1c(Cl)cccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL270254 197795 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 502 4 1 4 4.8 O=S(=O)(c1c(Cl)cccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
155561040 349376 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 418 6 2 5 2.7 CNS(=O)(=O)c1ccc(CNC(=O)c2cnn(-c3ccc(Cl)cc3)c2C)cc1 10.1016/j.bmcl.2018.11.015
CHEMBL4574870 349376 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 418 6 2 5 2.7 CNS(=O)(=O)c1ccc(CNC(=O)c2cnn(-c3ccc(Cl)cc3)c2C)cc1 10.1016/j.bmcl.2018.11.015
44453290 197728 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 482 4 1 4 4.4 Cc1cccc(Cl)c1S(=O)(=O)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL269956 197728 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 482 4 1 4 4.4 Cc1cccc(Cl)c1S(=O)(=O)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
59278286 336088 1 None -112 2 Mouse 7.4 pIC50 = 7.4 Functional
Antagonist activity at mouse CCR1 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at mouse CCR1 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 453 6 1 7 3.2 CC[C@H](NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4464625 336088 1 None -112 2 Mouse 7.4 pIC50 = 7.4 Functional
Antagonist activity at mouse CCR1 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at mouse CCR1 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 453 6 1 7 3.2 CC[C@H](NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
44469942 348976 0 None None None Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 452 6 1 5 3.3 CN(C)S(=O)(=O)c1cccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4565496 348976 0 None None None Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 452 6 1 5 3.3 CN(C)S(=O)(=O)c1cccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
25233582 373199 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 401 5 1 3 4.0 COc1ccc(NC(=O)N2CCC[C@@H]2C(=O)N(C)Cc2ccc(Cl)cc2)cc1 10.1021/jm801416q
CHEMBL517290 373199 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 401 5 1 3 4.0 COc1ccc(NC(=O)N2CCC[C@@H]2C(=O)N(C)Cc2ccc(Cl)cc2)cc1 10.1021/jm801416q
44309245 468458 0 None None None Human 6.4 pIC50 = 6.4 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 556 13 3 5 5.2 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)NCc1ccccc1 10.1016/j.bmcl.2004.02.022
CHEMBL65784 468458 0 None None None Human 6.4 pIC50 = 6.4 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 556 13 3 5 5.2 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)NCc1ccccc1 10.1016/j.bmcl.2004.02.022
10001921 144665 0 None -3 2 Mouse 6.4 pIC50 = 6.4 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 415 5 1 3 3.8 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)CC1 10.1016/j.bmcl.2005.08.057
CHEMBL198852 144665 0 None -3 2 Mouse 6.4 pIC50 = 6.4 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 415 5 1 3 3.8 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)CC1 10.1016/j.bmcl.2005.08.057
9980155 144042 0 None 23 2 Human 7.4 pIC50 = 7.4 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 430 5 2 3 3.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1NC(N)=O 10.1016/j.bmcl.2005.08.057
CHEMBL196860 144042 0 None 23 2 Human 7.4 pIC50 = 7.4 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 430 5 2 3 3.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1NC(N)=O 10.1016/j.bmcl.2005.08.057
45138012 334767 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 414 4 1 4 4.5 O=C(NCc1cccc(C(F)(F)F)c1)c1nccc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4445316 334767 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 414 4 1 4 4.5 O=C(NCc1cccc(C(F)(F)F)c1)c1nccc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
58138781 349123 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 379 4 1 3 4.7 O=C(NCc1cccc(Cl)c1)c1cccc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4568987 349123 0 None None None Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 379 4 1 3 4.7 O=C(NCc1cccc(Cl)c1)c1cccc2c1cnn2-c1ccc(F)cc1 10.1016/j.bmcl.2018.12.024
44453198 195981 0 None None None Human 5.3 pIC50 = 5.3 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 516 4 1 4 5.2 CC1(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN(S(=O)(=O)c2c(Cl)cccc2Cl)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL257853 195981 0 None None None Human 5.3 pIC50 = 5.3 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 516 4 1 4 5.2 CC1(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN(S(=O)(=O)c2c(Cl)cccc2Cl)CC1 10.1016/j.bmcl.2007.09.068
44430746 177992 0 None 41 2 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 530 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCO)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232638 177992 0 None 41 2 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 530 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCO)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44480348 349760 0 None None None Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 446 7 1 6 3.9 CCCC(NC(=O)c1cnn(-c2ccc(Cl)cc2)c1C)c1ccc(S(C)(=O)=O)nc1 10.1016/j.bmcl.2018.11.015
CHEMBL4583870 349760 0 None None None Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 446 7 1 6 3.9 CCCC(NC(=O)c1cnn(-c2ccc(Cl)cc2)c1C)c1ccc(S(C)(=O)=O)nc1 10.1016/j.bmcl.2018.11.015
44453639 314727 0 None None None Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 482 4 1 4 4.4 Cc1cccc(Cl)c1S(=O)(=O)N1CCC[C@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
CHEMBL409498 314727 0 None None None Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 482 4 1 4 4.4 Cc1cccc(Cl)c1S(=O)(=O)N1CCC[C@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
44405203 144699 0 None -31 2 Mouse 5.3 pIC50 = 5.3 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 443 4 1 4 4.5 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)oc12 10.1016/j.bmcl.2005.08.057
CHEMBL198966 144699 0 None -31 2 Mouse 5.3 pIC50 = 5.3 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 443 4 1 4 4.5 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)oc12 10.1016/j.bmcl.2005.08.057
10503785 239731 0 None None None Human 5.3 pIC50 = 5.3 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 451 7 1 4 5.3 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)N1CCCCC1 10.1021/jm990316l
CHEMBL357434 239731 0 None None None Human 5.3 pIC50 = 5.3 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 451 7 1 4 5.3 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)N1CCCCC1 10.1021/jm990316l
59687824 155196 0 None None None Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at CCR1Antagonist activity at CCR1
ChEMBL 469 5 1 5 3.6 CO[C@@H]1COCC[C@@H]1NC1CC[C@@](C(=O)N2CCc3ncc(C(F)(F)F)cc3C2)(C(C)C)C1 10.1021/jm300682j
CHEMBL2178572 155196 0 None None None Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at CCR1Antagonist activity at CCR1
ChEMBL 469 5 1 5 3.6 CO[C@@H]1COCC[C@@H]1NC1CC[C@@](C(=O)N2CCc3ncc(C(F)(F)F)cc3C2)(C(C)C)C1 10.1021/jm300682j
44430753 279194 0 None 77 2 Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 598 11 3 9 2.2 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCNCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL387608 279194 0 None 77 2 Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 598 11 3 9 2.2 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCNCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44470083 336111 0 None None None Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 466 7 2 5 3.8 CC(C)NS(=O)(=O)c1ccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4465000 336111 0 None None None Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 466 7 2 5 3.8 CC(C)NS(=O)(=O)c1ccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)cc1 10.1016/j.bmcl.2018.12.024
44309312 468765 0 None None None Human 8.3 pIC50 = 8.3 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 460 9 3 5 3.4 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCCC1 10.1016/j.bmcl.2004.02.022
44309337 468765 0 None None None Human 8.3 pIC50 = 8.3 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 460 9 3 5 3.4 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCCC1 10.1016/j.bmcl.2004.02.022
CHEMBL68145 468765 0 None None None Human 8.3 pIC50 = 8.3 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 460 9 3 5 3.4 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCCC1 10.1016/j.bmcl.2004.02.022
CHEMBL69375 468765 0 None None None Human 8.3 pIC50 = 8.3 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 460 9 3 5 3.4 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCCC1 10.1016/j.bmcl.2004.02.022
21070989 177765 0 None 354 2 Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced calcium flux by FLIPR assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced calcium flux by FLIPR assay
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None 354 2 Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced calcium flux by FLIPR assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced calcium flux by FLIPR assay
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
44453200 196032 0 None None None Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.0 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1C(F)(F)F 10.1016/j.bmcl.2007.09.068
CHEMBL258065 196032 0 None None None Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 476 7 2 4 4.0 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1C(F)(F)F 10.1016/j.bmcl.2007.09.068
44405181 260685 0 None 51 2 Human 7.3 pIC50 = 7.3 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 432 6 2 4 3.6 CC(=O)Nc1cc(Cl)ccc1NCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL370162 260685 0 None 51 2 Human 7.3 pIC50 = 7.3 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 432 6 2 4 3.6 CC(=O)Nc1cc(Cl)ccc1NCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
10434371 145166 0 None -5 2 Mouse 7.3 pIC50 = 7.3 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 459 6 1 4 4.2 COc1cc(/C=C/C(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
CHEMBL200629 145166 0 None -5 2 Mouse 7.3 pIC50 = 7.3 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 459 6 1 4 4.2 COc1cc(/C=C/C(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
44405212 145177 0 None -1 2 Mouse 7.3 pIC50 = 7.3 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 458 5 1 4 4.2 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
CHEMBL200680 145177 0 None -1 2 Mouse 7.3 pIC50 = 7.3 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 458 5 1 4 4.2 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
155549724 347937 0 None None None Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 427 4 1 3 5.4 Cc1c(C(=O)NCc2cccc(C(F)(F)F)c2)cnn1-c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2018.11.015
CHEMBL4539264 347937 0 None None None Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 427 4 1 3 5.4 Cc1c(C(=O)NCc2cccc(C(F)(F)F)c2)cnn1-c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2018.11.015
10388824 270926 0 None -4 2 Mouse 6.3 pIC50 = 6.3 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 445 5 1 3 4.7 CC(=O)Nc1cc2ccccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL370596 270926 0 None -4 2 Mouse 6.3 pIC50 = 6.3 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 445 5 1 3 4.7 CC(=O)Nc1cc2ccccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
9870185 175084 0 None None None Human 5.3 pIC50 = 5.3 Functional
Antagonist activity at CCR1Antagonist activity at CCR1
ChEMBL 489 7 3 5 3.5 O=C(NC[C@@H](O)CN1CCC(Oc2ccc(Cl)c(Cl)c2)CC1)c1c[nH]c(=O)c2ccccc12 10.1016/j.bmcl.2012.09.113
CHEMBL2207666 175084 0 None None None Human 5.3 pIC50 = 5.3 Functional
Antagonist activity at CCR1Antagonist activity at CCR1
ChEMBL 489 7 3 5 3.5 O=C(NC[C@@H](O)CN1CCC(Oc2ccc(Cl)c(Cl)c2)CC1)c1c[nH]c(=O)c2ccccc12 10.1016/j.bmcl.2012.09.113
162658125 354955 0 None -125 3 Human 5.3 pIC50 = 5.3 Functional
Antagonist activity at human CCR1 expressed in human U2OS cell membranes as inhibition of [35S]GTPgammaS binding pre-incubated for 30 mins before CCL3 stimulation and followed by further incubation for 90 mins by scintillation counting methodAntagonist activity at human CCR1 expressed in human U2OS cell membranes as inhibition of [35S]GTPgammaS binding pre-incubated for 30 mins before CCL3 stimulation and followed by further incubation for 90 mins by scintillation counting method
ChEMBL 471 6 2 4 5.9 O=C(O)c1ccc(Oc2ccc(Cl)cc2NS(=O)(=O)c2ccc(Cl)c(Cl)c2)cc1 10.1021/acs.jmedchem.0c01137
CHEMBL4760108 354955 0 None -125 3 Human 5.3 pIC50 = 5.3 Functional
Antagonist activity at human CCR1 expressed in human U2OS cell membranes as inhibition of [35S]GTPgammaS binding pre-incubated for 30 mins before CCL3 stimulation and followed by further incubation for 90 mins by scintillation counting methodAntagonist activity at human CCR1 expressed in human U2OS cell membranes as inhibition of [35S]GTPgammaS binding pre-incubated for 30 mins before CCL3 stimulation and followed by further incubation for 90 mins by scintillation counting method
ChEMBL 471 6 2 4 5.9 O=C(O)c1ccc(Oc2ccc(Cl)cc2NS(=O)(=O)c2ccc(Cl)c(Cl)c2)cc1 10.1021/acs.jmedchem.0c01137
162666730 356101 1 None -707 3 Human 5.3 pIC50 = 5.3 Functional
Antagonist activity at human CCR1 expressed in human U2OS cell membranes as inhibition of [35S]GTPgammaS binding pre-incubated for 30 mins before CCL3 stimulation and followed by further incubation for 90 mins by scintillation counting methodAntagonist activity at human CCR1 expressed in human U2OS cell membranes as inhibition of [35S]GTPgammaS binding pre-incubated for 30 mins before CCL3 stimulation and followed by further incubation for 90 mins by scintillation counting method
ChEMBL 589 9 2 6 6.5 N#CSCCNC(=O)c1ccc(Oc2ccc(Cl)cc2NS(=O)(=O)c2ccc(Cl)c(C(F)(F)F)c2)cc1 10.1021/acs.jmedchem.0c01137
CHEMBL4783861 356101 1 None -707 3 Human 5.3 pIC50 = 5.3 Functional
Antagonist activity at human CCR1 expressed in human U2OS cell membranes as inhibition of [35S]GTPgammaS binding pre-incubated for 30 mins before CCL3 stimulation and followed by further incubation for 90 mins by scintillation counting methodAntagonist activity at human CCR1 expressed in human U2OS cell membranes as inhibition of [35S]GTPgammaS binding pre-incubated for 30 mins before CCL3 stimulation and followed by further incubation for 90 mins by scintillation counting method
ChEMBL 589 9 2 6 6.5 N#CSCCNC(=O)c1ccc(Oc2ccc(Cl)cc2NS(=O)(=O)c2ccc(Cl)c(C(F)(F)F)c2)cc1 10.1021/acs.jmedchem.0c01137
44453436 197950 0 None None None Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 458 7 2 4 4.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc2ccccc2c1 10.1016/j.bmcl.2007.09.068
CHEMBL271079 197950 0 None None None Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 458 7 2 4 4.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc2ccccc2c1 10.1016/j.bmcl.2007.09.068
44453293 332188 0 None None None Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 486 7 2 4 3.8 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1Br 10.1016/j.bmcl.2007.09.068
CHEMBL429591 332188 0 None None None Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 486 7 2 4 3.8 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1Br 10.1016/j.bmcl.2007.09.068
9869274 238077 0 None None None Human 5.3 pIC50 = 5.3 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 468 5 1 3 6.4 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2C=Cc2ccccc21 10.1021/jm990316l
CHEMBL344073 238077 0 None None None Human 5.3 pIC50 = 5.3 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 468 5 1 3 6.4 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2C=Cc2ccccc21 10.1021/jm990316l
44430745 279221 0 None None None Human 7.3 pIC50 = 7.3 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 544 11 2 8 3.0 COCCNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL387822 279221 0 None None None Human 7.3 pIC50 = 7.3 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 544 11 2 8 3.0 COCCNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
10111333 349467 0 None -19 2 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 395 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4577133 349467 0 None -19 2 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 395 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
58138841 334206 0 None None None Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 438 6 2 5 3.0 CNS(=O)(=O)c1cccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4437170 334206 0 None None None Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 438 6 2 5 3.0 CNS(=O)(=O)c1cccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
512282 1562 44 None 141 4 Human 6.3 pIC50 = 6.3 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
767 1562 44 None 141 4 Human 6.3 pIC50 = 6.3 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
CHEMBL232656 1562 44 None 141 4 Human 6.3 pIC50 = 6.3 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2005.08.057
44405202 145203 0 None 17 2 Human 6.3 pIC50 = 6.3 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 442 4 2 3 4.3 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)[nH]c12 10.1016/j.bmcl.2005.08.057
CHEMBL200794 145203 0 None 17 2 Human 6.3 pIC50 = 6.3 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 442 4 2 3 4.3 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)[nH]c12 10.1016/j.bmcl.2005.08.057
10576419 77690 0 None None None Human 5.3 pIC50 = 5.3 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 472 9 1 3 6.7 N#CC(CCCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL142620 77690 0 None None None Human 5.3 pIC50 = 5.3 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 472 9 1 3 6.7 N#CC(CCCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL3138380 477898 0 None None None Human 5.2 pIC50 = 5.2 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 1036 20 2 8 16.3 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(OCc6cccc([N+](=O)[O-])c6)c(C(=O)O)c5)c5cc(Cl)c(OCc6cccc([N+](=O)[O-])c6)c(C(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
CHEMBL3138437 477898 0 None None None Human 5.2 pIC50 = 5.2 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 1036 20 2 8 16.3 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(OCc6cccc([N+](=O)[O-])c6)c(C(=O)O)c5)c5cc(Cl)c(OCc6cccc([N+](=O)[O-])c6)c(C(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
10001921 144665 0 None 3 2 Human 7.2 pIC50 = 7.2 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 415 5 1 3 3.8 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)CC1 10.1016/j.bmcl.2005.08.057
CHEMBL198852 144665 0 None 3 2 Human 7.2 pIC50 = 7.2 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 415 5 1 3 3.8 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)CC1 10.1016/j.bmcl.2005.08.057
11743399 144696 8 None -32 2 Mouse 6.2 pIC50 = 6.2 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 429 5 1 3 4.2 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL198949 144696 8 None -32 2 Mouse 6.2 pIC50 = 6.2 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 429 5 1 3 4.2 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
10572669 238197 0 None None None Human 5.2 pIC50 = 5.2 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 393 6 1 4 4.6 N#Cc1ccccc1C(C#N)CCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
CHEMBL344989 238197 0 None None None Human 5.2 pIC50 = 5.2 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 393 6 1 4 4.6 N#Cc1ccccc1C(C#N)CCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
3497 2447 26 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2018.11.015
44309353 2447 26 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2018.11.015
5311123 2447 26 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2018.11.015
CHEMBL1628706 2447 26 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2018.11.015
CHEMBL308473 2447 26 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2018.11.015
44453499 311371 0 None None None Human 6.2 pIC50 = 6.2 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 486 4 1 4 4.3 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(F)c(Cl)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL403613 311371 0 None None None Human 6.2 pIC50 = 6.2 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 486 4 1 4 4.3 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(F)c(Cl)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
10111333 349467 0 None -19 2 Human 6.2 pIC50 = 6.2 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 395 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4577133 349467 0 None -19 2 Human 6.2 pIC50 = 6.2 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 395 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
44430748 178095 0 None 72 2 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 529 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232837 178095 0 None 72 2 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 529 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44430758 279954 0 None None None Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 482 6 2 6 3.1 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1Nc1c(N)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL389293 279954 0 None None None Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 482 6 2 6 3.1 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1Nc1c(N)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
25233756 354749 0 None None None Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 467 4 1 2 5.6 Cc1cc(C(F)(F)F)cc(C)c1NC(=O)N1CCC[C@@H]1C(=O)N(C)Cc1ccc(Cl)cc1 10.1021/jm801416q
CHEMBL475748 354749 0 None None None Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrsAntagonist activity at human CCR1 in THP1 cells assessed as inhibition of MIP-1-alpha-induced chemotaxis after 3 hrs
ChEMBL 467 4 1 2 5.6 Cc1cc(C(F)(F)F)cc(C)c1NC(=O)N1CCC[C@@H]1C(=O)N(C)Cc1ccc(Cl)cc1 10.1021/jm801416q
58138880 336873 0 None None None Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 452 6 1 5 3.3 CN(C)S(=O)(=O)c1ccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4475918 336873 0 None None None Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 452 6 1 5 3.3 CN(C)S(=O)(=O)c1ccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)cc1 10.1016/j.bmcl.2018.12.024
44405212 145177 0 None 1 2 Human 8.2 pIC50 = 8.2 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 458 5 1 4 4.2 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
CHEMBL200680 145177 0 None 1 2 Human 8.2 pIC50 = 8.2 Functional
Antagonistic activity at rat CCR1 in CHO-K1 cellsAntagonistic activity at rat CCR1 in CHO-K1 cells
ChEMBL 458 5 1 4 4.2 CC(=O)Nc1cc2ncccc2cc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
25253284 40074 0 None None None Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrsAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrs
ChEMBL 450 4 1 5 4.8 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCC[C@@H]1c1nnnn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
CHEMBL1224119 40074 0 None None None Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrsAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3-induced chemotaxis after 3 hrs
ChEMBL 450 4 1 5 4.8 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCC[C@@H]1c1nnnn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
59278314 334482 29 None 54 2 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 425 5 1 7 2.3 CS(=O)(=O)c1cc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)ccn1 10.1016/j.bmcl.2018.12.024
CHEMBL4441094 334482 29 None 54 2 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 425 5 1 7 2.3 CS(=O)(=O)c1cc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)ccn1 10.1016/j.bmcl.2018.12.024
11211557 334419 0 None None None Human 6.2 pIC50 = 6.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 393 4 1 3 4.8 Cc1c(C(=O)NCc2cccc(C(F)(F)F)c2)cnn1-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.11.015
CHEMBL4440166 334419 0 None None None Human 6.2 pIC50 = 6.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 393 4 1 3 4.8 Cc1c(C(=O)NCc2cccc(C(F)(F)F)c2)cnn1-c1ccc(Cl)cc1 10.1016/j.bmcl.2018.11.015
10456104 144205 0 None -56 2 Mouse 6.2 pIC50 = 6.2 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL197375 144205 0 None -56 2 Mouse 6.2 pIC50 = 6.2 Functional
Antagonistic activity at mouse CCR1 in CHO-K1 cellsAntagonistic activity at mouse CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
59278235 347198 0 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 425 5 1 7 2.3 CS(=O)(=O)c1cncc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4519965 347198 0 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 425 5 1 7 2.3 CS(=O)(=O)c1cncc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
44468708 348731 0 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 423 5 1 5 3.5 CS(=O)(=O)c1cccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4559388 348731 0 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 423 5 1 5 3.5 CS(=O)(=O)c1cccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
44453466 311588 0 None None None Human 6.2 pIC50 = 6.2 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 486 4 1 4 4.3 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)c(F)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL404757 311588 0 None None None Human 6.2 pIC50 = 6.2 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 486 4 1 4 4.3 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)c(F)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44453502 311135 0 None None None Human 5.2 pIC50 = 5.2 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3cccc(Cl)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL402110 311135 0 None None None Human 5.2 pIC50 = 5.2 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3cccc(Cl)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
3497 2447 26 None None None Human 7.2 pIC50 = 7.2 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2004.02.022
44309353 2447 26 None None None Human 7.2 pIC50 = 7.2 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2004.02.022
5311123 2447 26 None None None Human 7.2 pIC50 = 7.2 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2004.02.022
CHEMBL1628706 2447 26 None None None Human 7.2 pIC50 = 7.2 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2004.02.022
CHEMBL308473 2447 26 None None None Human 7.2 pIC50 = 7.2 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2004.02.022
44453226 196101 0 None None None Human 6.2 pIC50 = 6.2 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 536 4 1 4 5.4 O=S(=O)(c1ccc(Cl)c(Cl)c1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL258369 196101 0 None None None Human 6.2 pIC50 = 6.2 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 536 4 1 4 5.4 O=S(=O)(c1ccc(Cl)c(Cl)c1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
59278314 334482 29 None -54 2 Mouse 6.2 pIC50 = 6.2 Functional
Antagonist activity at mouse CCR1 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at mouse CCR1 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 425 5 1 7 2.3 CS(=O)(=O)c1cc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)ccn1 10.1016/j.bmcl.2018.12.024
CHEMBL4441094 334482 29 None -54 2 Mouse 6.2 pIC50 = 6.2 Functional
Antagonist activity at mouse CCR1 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at mouse CCR1 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 425 5 1 7 2.3 CS(=O)(=O)c1cc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)ccn1 10.1016/j.bmcl.2018.12.024
44468570 336398 0 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 423 5 1 5 3.5 CS(=O)(=O)c1ccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)cc1 10.1016/j.bmcl.2018.12.024
CHEMBL4469176 336398 0 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 423 5 1 5 3.5 CS(=O)(=O)c1ccc(CNC(=O)c2cccc3c2cnn3-c2ccc(F)cc2)cc1 10.1016/j.bmcl.2018.12.024
44309219 202205 0 None None None Human 7.2 pIC50 = 7.2 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 512 9 4 6 2.8 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1(O)CCC(F)(F)CC1 10.1016/j.bmcl.2004.02.022
CHEMBL302320 202205 0 None None None Human 7.2 pIC50 = 7.2 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 512 9 4 6 2.8 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1(O)CCC(F)(F)CC1 10.1016/j.bmcl.2004.02.022
44309313 202594 0 None None None Human 6.2 pIC50 = 6.2 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 482 11 4 6 2.5 CC(C)(O)CCC(C[C@H](O)[C@H](Cc1ccccc1F)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
CHEMBL304053 202594 0 None None None Human 6.2 pIC50 = 6.2 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 482 11 4 6 2.5 CC(C)(O)CCC(C[C@H](O)[C@H](Cc1ccccc1F)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
10434371 145166 0 None 5 2 Human 7.2 pIC50 = 7.2 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 459 6 1 4 4.2 COc1cc(/C=C/C(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
CHEMBL200629 145166 0 None 5 2 Human 7.2 pIC50 = 7.2 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 459 6 1 4 4.2 COc1cc(/C=C/C(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
17753030 177887 0 None 39 2 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 486 7 2 7 2.5 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(N)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232441 177887 0 None 39 2 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxisAntagonist activity against human CCR1 receptor expressed in THP1 cells assessed as inhibition of chemotaxis
ChEMBL 486 7 2 7 2.5 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(N)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44405176 272843 0 None 1 2 Human 8.2 pIC50 = 8.2 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 471 6 1 4 4.3 COc1cc(/C=C/C(=O)N2C3CCC2CN(Cc2ccc(F)cc2)C3)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
CHEMBL372807 272843 0 None 1 2 Human 8.2 pIC50 = 8.2 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 471 6 1 4 4.3 COc1cc(/C=C/C(=O)N2C3CCC2CN(Cc2ccc(F)cc2)C3)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
44405176 272843 0 None 1 2 Human 8.1 pIC50 = 8.1 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 471 6 1 4 4.3 COc1cc(/C=C/C(=O)N2C3CCC2CN(Cc2ccc(F)cc2)C3)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
CHEMBL372807 272843 0 None 1 2 Human 8.1 pIC50 = 8.1 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 471 6 1 4 4.3 COc1cc(/C=C/C(=O)N2C3CCC2CN(Cc2ccc(F)cc2)C3)c(NC(C)=O)cc1Cl 10.1016/j.bmcl.2005.08.057
44453529 198142 0 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 414 7 2 5 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccs1 10.1016/j.bmcl.2007.09.068
CHEMBL272097 198142 0 None None None Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 414 7 2 5 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccs1 10.1016/j.bmcl.2007.09.068
10076510 25915 0 None None None Human 6.2 pIC50 = 6.2 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 433 6 1 2 6.0 C[N+]1(CCCC(C#N)c2ccc3ccccc3c2)CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
CHEMBL1180795 25915 0 None None None Human 6.2 pIC50 = 6.2 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 433 6 1 2 6.0 C[N+]1(CCCC(C#N)c2ccc3ccccc3c2)CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
5311125 78652 0 None None None Human 5.2 pIC50 = 5.2 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 488 5 1 4 6.5 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
CHEMBL143492 78652 0 None None None Human 5.2 pIC50 = 5.2 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 488 5 1 4 6.5 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
10717972 238111 0 None None None Human 5.2 pIC50 = 5.2 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 440 8 1 5 4.4 CCOC(=O)C(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
CHEMBL344324 238111 0 None None None Human 5.2 pIC50 = 5.2 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 440 8 1 5 4.4 CCOC(=O)C(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
44309077 469245 0 None None None Human 5.2 pIC50 = 5.2 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 549 11 2 6 3.6 CN1CCN(C(=O)C(CCC(C)(C)F)C[C@H](O)[C@H](Cc2ccccc2)NC(=O)c2cnc3ccccc3n2)CC1 10.1016/j.bmcl.2004.02.022
CHEMBL71499 469245 0 None None None Human 5.2 pIC50 = 5.2 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 549 11 2 6 3.6 CN1CCN(C(=O)C(CCC(C)(C)F)C[C@H](O)[C@H](Cc2ccccc2)NC(=O)c2cnc3ccccc3n2)CC1 10.1016/j.bmcl.2004.02.022
10695080 26473 0 None None None Human 5.2 pIC50 = 5.2 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 418 6 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc2ccccc2c1 10.1021/jm990316l
CHEMBL1184276 26473 0 None None None Human 5.2 pIC50 = 5.2 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 418 6 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc2ccccc2c1 10.1021/jm990316l
44453163 311382 0 None None None Human 5.1 pIC50 = 5.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 454 4 1 5 3.9 CC1(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN(S(=O)(=O)c2cccs2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL403692 311382 0 None None None Human 5.1 pIC50 = 5.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 454 4 1 5 3.9 CC1(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN(S(=O)(=O)c2cccs2)CC1 10.1016/j.bmcl.2007.09.068
44309124 468838 0 None None None Human 6.1 pIC50 = 6.1 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 520 11 2 5 4.5 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)N1CCCC1 10.1016/j.bmcl.2004.02.022
CHEMBL68692 468838 0 None None None Human 6.1 pIC50 = 6.1 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 520 11 2 5 4.5 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)N1CCCC1 10.1016/j.bmcl.2004.02.022
58138788 335697 0 None None None Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 395 4 1 3 5.0 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1ccccc1 10.1016/j.bmcl.2018.12.024
CHEMBL4458721 335697 0 None None None Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 395 4 1 3 5.0 O=C(NCc1cccc(C(F)(F)F)c1)c1cccc2c1cnn2-c1ccccc1 10.1016/j.bmcl.2018.12.024
9956488 238012 0 None None None Human 5.1 pIC50 = 5.1 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 472 5 1 4 5.8 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2COc2ccccc21 10.1021/jm990316l
CHEMBL343511 238012 0 None None None Human 5.1 pIC50 = 5.1 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 472 5 1 4 5.8 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2COc2ccccc21 10.1021/jm990316l
9956380 332961 0 None None None Human 5.1 pIC50 = 5.1 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 470 5 1 3 6.0 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2CCc2ccccc21 10.1021/jm990316l
CHEMBL433746 332961 0 None None None Human 5.1 pIC50 = 5.1 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 470 5 1 3 6.0 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2CCc2ccccc21 10.1021/jm990316l
24758044 164277 0 None 5 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis incubated for 60 mins at 37 degCAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis incubated for 60 mins at 37 degC
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57888953 164277 0 None 5 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis incubated for 60 mins at 37 degCAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis incubated for 60 mins at 37 degC
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
71455572 164277 0 None 5 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis incubated for 60 mins at 37 degCAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis incubated for 60 mins at 37 degC
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180523 164277 0 None 5 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis incubated for 60 mins at 37 degCAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis incubated for 60 mins at 37 degC
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180528 164277 0 None 5 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis incubated for 60 mins at 37 degCAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis incubated for 60 mins at 37 degC
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180534 164277 0 None 5 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis incubated for 60 mins at 37 degCAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis incubated for 60 mins at 37 degC
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
37664972 335049 0 None None None Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 377 4 1 3 4.3 Cc1c(C(=O)NCc2cccc(C(F)(F)F)c2)cnn1-c1ccc(F)cc1 10.1016/j.bmcl.2018.11.015
CHEMBL4449368 335049 0 None None None Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 377 4 1 3 4.3 Cc1c(C(=O)NCc2cccc(C(F)(F)F)c2)cnn1-c1ccc(F)cc1 10.1016/j.bmcl.2018.11.015
44453317 197751 0 None None None Human 5.1 pIC50 = 5.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 480 5 1 5 4.2 CSc1ccc(C2(O)CCN(C3CCN(S(=O)(=O)c4ccccc4Cl)CC3)CC2)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL270033 197751 0 None None None Human 5.1 pIC50 = 5.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 480 5 1 5 4.2 CSc1ccc(C2(O)CCN(C3CCN(S(=O)(=O)c4ccccc4Cl)CC3)CC2)cc1 10.1016/j.bmcl.2007.09.068
44430755 309540 0 None 42 2 Human 8.1 pIC50 = 8.1 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 577 10 2 8 3.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2cccnc2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL397910 309540 0 None 42 2 Human 8.1 pIC50 = 8.1 Functional
Antagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPRAntagonist activity at human CCR1 expressed in THP1 cells assessed as effect on MIP-1-alpha-induced calcium flux by FLIPR
ChEMBL 577 10 2 8 3.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2cccnc2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
59278123 336868 0 None None None Human 8.1 pIC50 = 8.1 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 424 5 1 6 2.9 CS(=O)(=O)c1cccc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4475801 336868 0 None None None Human 8.1 pIC50 = 8.1 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 424 5 1 6 2.9 CS(=O)(=O)c1cccc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)c1 10.1016/j.bmcl.2018.12.024
44309286 202416 0 None None None Human 8.1 pIC50 = 8.1 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 512 9 4 6 3.7 O=C(N[C@@H](Cc1ccccc1)[C@@H](O)CC(C(=O)NO)C1CCC(F)(F)CC1)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.022
CHEMBL303673 202416 0 None None None Human 8.1 pIC50 = 8.1 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 512 9 4 6 3.7 O=C(N[C@@H](Cc1ccccc1)[C@@H](O)CC(C(=O)NO)C1CCC(F)(F)CC1)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.022
44453228 195769 0 None None None Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 426 7 2 4 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1F 10.1016/j.bmcl.2007.09.068
CHEMBL256888 195769 0 None None None Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 426 7 2 4 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1F 10.1016/j.bmcl.2007.09.068
10388824 270926 0 None 4 2 Human 7.1 pIC50 = 7.1 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 445 5 1 3 4.7 CC(=O)Nc1cc2ccccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL370596 270926 0 None 4 2 Human 7.1 pIC50 = 7.1 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 445 5 1 3 4.7 CC(=O)Nc1cc2ccccc2cc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
44405196 277849 0 None None None Human 6.1 pIC50 = 6.1 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 460 5 2 4 3.8 COc1cc2c(cc1Cl)NC(=O)NC2CC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL381223 277849 0 None None None Human 6.1 pIC50 = 6.1 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 460 5 2 4 3.8 COc1cc2c(cc1Cl)NC(=O)NC2CC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
44453641 198235 0 None None None Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 438 8 2 5 3.0 COc1ccc(S(=O)(=O)NCCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL272559 198235 0 None None None Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 438 8 2 5 3.0 COc1ccc(S(=O)(=O)NCCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1 10.1016/j.bmcl.2007.09.068
10789482 67301 0 None None None Human 5.1 pIC50 = 5.1 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 444 9 1 3 5.9 N#CC(CCCCl)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
CHEMBL142191 67301 0 None None None Human 5.1 pIC50 = 5.1 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 444 9 1 3 5.9 N#CC(CCCCl)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
44453584 198222 0 None None None Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 484 8 2 4 4.7 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1-c1ccccc1 10.1016/j.bmcl.2007.09.068
CHEMBL272523 198222 0 None None None Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 484 8 2 4 4.7 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1-c1ccccc1 10.1016/j.bmcl.2007.09.068
44308819 203236 0 None None None Human 6.1 pIC50 = 6.1 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.022
44308902 203236 0 None None None Human 6.1 pIC50 = 6.1 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.022
CHEMBL308243 203236 0 None None None Human 6.1 pIC50 = 6.1 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.022
CHEMBL68937 203236 0 None None None Human 6.1 pIC50 = 6.1 Functional
Inhibition of CCL3 induced chemotaxis in human T lymphocytesInhibition of CCL3 induced chemotaxis in human T lymphocytes
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.022
10547456 238325 0 None None None Human 5.1 pIC50 = 5.1 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 374 6 1 4 4.8 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccs1 10.1021/jm990316l
CHEMBL346205 238325 0 None None None Human 5.1 pIC50 = 5.1 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 374 6 1 4 4.8 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccs1 10.1021/jm990316l
24758044 164277 0 None 5 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CK-8beta-induced calcium flux by FLIPRAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CK-8beta-induced calcium flux by FLIPR
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57888953 164277 0 None 5 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CK-8beta-induced calcium flux by FLIPRAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CK-8beta-induced calcium flux by FLIPR
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
71455572 164277 0 None 5 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CK-8beta-induced calcium flux by FLIPRAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CK-8beta-induced calcium flux by FLIPR
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180523 164277 0 None 5 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CK-8beta-induced calcium flux by FLIPRAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CK-8beta-induced calcium flux by FLIPR
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180528 164277 0 None 5 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CK-8beta-induced calcium flux by FLIPRAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CK-8beta-induced calcium flux by FLIPR
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180534 164277 0 None 5 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CK-8beta-induced calcium flux by FLIPRAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CK-8beta-induced calcium flux by FLIPR
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
155514261 334402 0 None 1 2 Human 5.1 pIC50 = 5.1 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 493 4 1 3 5.2 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1c1cccc(Br)c1)C1CC1 10.1021/acs.jmedchem.8b00605
CHEMBL4439854 334402 0 None 1 2 Human 5.1 pIC50 = 5.1 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 493 4 1 3 5.2 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1c1cccc(Br)c1)C1CC1 10.1021/acs.jmedchem.8b00605
155514261 334402 0 None 1 2 Human 5.1 pIC50 = 5.1 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 493 4 1 3 5.2 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1c1cccc(Br)c1)C1CC1 10.1021/acs.jmedchem.8b00605
CHEMBL4439854 334402 0 None 1 2 Human 5.1 pIC50 = 5.1 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 493 4 1 3 5.2 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1c1cccc(Br)c1)C1CC1 10.1021/acs.jmedchem.8b00605
10526132 144690 0 None -1 2 Human 5.1 pIC50 = 5.1 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 419 7 1 2 6.2 OC1(c2ccc(Cl)cc2)CCN(CCCC(c2ccccc2)c2ccccc2)CC1 10.1021/jm990316l
CHEMBL198935 144690 0 None -1 2 Human 5.1 pIC50 = 5.1 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 419 7 1 2 6.2 OC1(c2ccc(Cl)cc2)CCN(CCCC(c2ccccc2)c2ccccc2)CC1 10.1021/jm990316l
11554849 145064 0 None 2 2 Human 8.1 pIC50 = 8.1 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 484 7 1 4 3.9 CN(C)CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
CHEMBL200242 145064 0 None 2 2 Human 8.1 pIC50 = 8.1 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 484 7 1 4 3.9 CN(C)CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C2CCC1CN(Cc1ccc(F)cc1)C2 10.1016/j.bmcl.2005.08.057
10456104 144205 0 None 56 2 Human 8.1 pIC50 = 8.1 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL197375 144205 0 None 56 2 Human 8.1 pIC50 = 8.1 Functional
Antagonistic activity at human CCR1 in CHO-K1 cellsAntagonistic activity at human CCR1 in CHO-K1 cells
ChEMBL 443 5 1 3 4.6 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
3536 8490 0 None 9 2 Human 8.0 pIC50 = 8.0 Functional
Antagonist activity at CCR1 assessed as inhibition of CCL3-induced chemotaxis by cell based assayAntagonist activity at CCR1 assessed as inhibition of CCL3-induced chemotaxis by cell based assay
ChEMBL 515 5 1 2 7.3 CC[N+]1(CCC(CC1)NC(=O)C1c2cc(Cl)ccc2Oc2c1cc(Cl)cc2)CC1CCCCCC1 10.1021/jm300682j
44560289 8490 0 None 9 2 Human 8.0 pIC50 = 8.0 Functional
Antagonist activity at CCR1 assessed as inhibition of CCL3-induced chemotaxis by cell based assayAntagonist activity at CCR1 assessed as inhibition of CCL3-induced chemotaxis by cell based assay
ChEMBL 515 5 1 2 7.3 CC[N+]1(CCC(CC1)NC(=O)C1c2cc(Cl)ccc2Oc2c1cc(Cl)cc2)CC1CCCCCC1 10.1021/jm300682j
CHEMBL1186993 8490 0 None 9 2 Human 8.0 pIC50 = 8.0 Functional
Antagonist activity at CCR1 assessed as inhibition of CCL3-induced chemotaxis by cell based assayAntagonist activity at CCR1 assessed as inhibition of CCL3-induced chemotaxis by cell based assay
ChEMBL 515 5 1 2 7.3 CC[N+]1(CCC(CC1)NC(=O)C1c2cc(Cl)ccc2Oc2c1cc(Cl)cc2)CC1CCCCCC1 10.1021/jm300682j
44405202 145203 0 None 17 2 Human 8.0 pIC50 = 8.0 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 442 4 2 3 4.3 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)[nH]c12 10.1016/j.bmcl.2005.08.057
CHEMBL200794 145203 0 None 17 2 Human 8.0 pIC50 = 8.0 Functional
Antagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cellsAntagonistic activity at human CCR1 by inhibition of MIP-1alpha induced calcium mobilization in THP1 cells
ChEMBL 442 4 2 3 4.3 CC(=O)Nc1cc(Cl)cc2cc(C(=O)N3CCN(Cc4ccc(F)cc4)C[C@H]3C)[nH]c12 10.1016/j.bmcl.2005.08.057
11743399 144696 8 None 32 2 Human 8.0 pIC50 = 8 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 429 5 1 3 4.2 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
CHEMBL198949 144696 8 None 32 2 Human 8.0 pIC50 = 8 Functional
Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1Inhibitory effect on transwell chemotaxis induced by 1 nM MIP-1alpha in mouse pre-B cells transfected with human CCR1
ChEMBL 429 5 1 3 4.2 CC(=O)Nc1cc(Cl)ccc1/C=C/C(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2005.08.057
44453359 197863 0 None None None Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 408 7 2 4 3.0 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1016/j.bmcl.2007.09.068
CHEMBL270631 197863 0 None None None Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 408 7 2 4 3.0 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1016/j.bmcl.2007.09.068
25022507 311387 0 None None None Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Br)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL403728 311387 0 None None None Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assayAntagonist activity at human CCR1 receptor expressed in THP1 cells assessed as human MIP-1-alpha-stimulated intracellular calcium level by FLIPR assay
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Br)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
10833944 237552 0 None None None Human 5.1 pIC50 = 5.1 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 384 6 2 4 4.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(O)c1 10.1021/jm990316l
CHEMBL341840 237552 0 None None None Human 5.1 pIC50 = 5.1 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 384 6 2 4 4.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(O)c1 10.1021/jm990316l
CHEMBL3138118 477895 0 None None None Human 5.0 pIC50 = 5.0 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 1187 22 4 6 19.2 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(OCc6ccc(-c7cccc(C(=O)O)c7)cc6)c(C(=O)O)c5)c5cc(Cl)c(OCc6ccc(-c7cccc(C(=O)O)c7)cc6)c(C(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
CHEMBL3138133 477895 0 None None None Human 5.0 pIC50 = 5.0 Functional
Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsInhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectants
ChEMBL 1187 22 4 6 19.2 CC(C)CCCC(C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](CCC=C(c5cc(Cl)c(OCc6ccc(-c7cccc(C(=O)O)c7)cc6)c(C(=O)O)c5)c5cc(Cl)c(OCc6ccc(-c7cccc(C(=O)O)c7)cc6)c(C(=O)O)c5)CC[C@]4(C)[C@H]3CC[C@@]21C 10.1016/s0960-894x(00)00601-6
155521447 335135 0 None -3 2 Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 421 4 1 3 4.7 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1)C1CC1 10.1021/acs.jmedchem.8b00605
CHEMBL4450561 335135 0 None -3 2 Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 421 4 1 3 4.7 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1)C1CC1 10.1021/acs.jmedchem.8b00605
155521447 335135 0 None -3 2 Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 421 4 1 3 4.7 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1)C1CC1 10.1021/acs.jmedchem.8b00605
CHEMBL4450561 335135 0 None -3 2 Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assayAntagonist activity at human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor assessed as reduction in CCL3-induced G-protein activation preincubated for 30 mins in presence of CCL3 followed by incubation of 90 mins by [35S]GTPgammaS binding assay
ChEMBL 421 4 1 3 4.7 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1)C1CC1 10.1021/acs.jmedchem.8b00605
155549273 347912 0 None None None Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 404 5 1 5 4.0 Cc1c(C(=O)NCc2cccc(C(F)(F)F)c2)cnn1-c1ccc([N+](=O)[O-])cc1 10.1016/j.bmcl.2018.11.015
CHEMBL4538794 347912 0 None None None Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assayAntagonist activity at recombinant CCR1 (unknown origin) expressed in non-adherent cells co-expressing Galpha16 assessed as inhibition of MIP-1 alpha-induced calcium flux by Fluo-4 NW or Calcium 4 dye based FLIPR TETRA assay
ChEMBL 404 5 1 5 4.0 Cc1c(C(=O)NCc2cccc(C(F)(F)F)c2)cnn1-c1ccc([N+](=O)[O-])cc1 10.1016/j.bmcl.2018.11.015
10690854 66372 0 None None None Human 5.0 pIC50 = 5.0 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 374 6 1 4 4.8 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccsc1 10.1021/jm990316l
CHEMBL141387 66372 0 None None None Human 5.0 pIC50 = 5.0 Functional
Inhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptorInhibition of MIP-1-alpha-induced intracellular calcium mobilization in HEK293 cells expressing human CCR1 receptor
ChEMBL 374 6 1 4 4.8 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccsc1 10.1021/jm990316l
49798289 24930 0 None None None Human 6.9 pKi = 6.9 Functional
Antagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrsAntagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrs
ChEMBL 489 6 2 4 5.8 O=C(O)c1c(F)cccc1Oc1ccc(C(F)(F)F)cc1NS(=O)(=O)c1ccc(Cl)cc1 10.1016/j.bmcl.2010.04.142
CHEMBL1170391 24930 0 None None None Human 6.9 pKi = 6.9 Functional
Antagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrsAntagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrs
ChEMBL 489 6 2 4 5.8 O=C(O)c1c(F)cccc1Oc1ccc(C(F)(F)F)cc1NS(=O)(=O)c1ccc(Cl)cc1 10.1016/j.bmcl.2010.04.142
49798265 25009 0 None None None Human 6.9 pKi = 6.9 Functional
Antagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrsAntagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrs
ChEMBL 489 6 2 4 5.8 O=C(O)c1ccccc1Oc1c(F)cc(C(F)(F)F)cc1NS(=O)(=O)c1ccc(Cl)cc1 10.1016/j.bmcl.2010.04.142
CHEMBL1171006 25009 0 None None None Human 6.9 pKi = 6.9 Functional
Antagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrsAntagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrs
ChEMBL 489 6 2 4 5.8 O=C(O)c1ccccc1Oc1c(F)cc(C(F)(F)F)cc1NS(=O)(=O)c1ccc(Cl)cc1 10.1016/j.bmcl.2010.04.142
10300214 175175 0 None None None Human 7.8 pKi = 7.8 Functional
Antagonist activity at CCR1Antagonist activity at CCR1
ChEMBL 492 9 2 5 5.0 O=C(Nc1ccccc1OCC(O)CN1CCC(Oc2ccc(Cl)c(Cl)c2)CC1)C1CCC1 10.1016/j.bmcl.2012.09.113
CHEMBL2208416 175175 0 None None None Human 7.8 pKi = 7.8 Functional
Antagonist activity at CCR1Antagonist activity at CCR1
ChEMBL 492 9 2 5 5.0 O=C(Nc1ccccc1OCC(O)CN1CCC(Oc2ccc(Cl)c(Cl)c2)CC1)C1CCC1 10.1016/j.bmcl.2012.09.113
49798264 25068 0 None None None Human 6.5 pKi = 6.5 Functional
Antagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrsAntagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrs
ChEMBL 403 6 2 4 4.6 O=C(O)c1ccccc1Oc1ccccc1NS(=O)(=O)c1ccc(Cl)cc1 10.1016/j.bmcl.2010.04.142
CHEMBL1171758 25068 0 None None None Human 6.5 pKi = 6.5 Functional
Antagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrsAntagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrs
ChEMBL 403 6 2 4 4.6 O=C(O)c1ccccc1Oc1ccccc1NS(=O)(=O)c1ccc(Cl)cc1 10.1016/j.bmcl.2010.04.142
19430534 25053 0 None None None Human 6.3 pKi = 6.3 Functional
Antagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrsAntagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrs
ChEMBL 471 6 2 4 5.7 O=C(O)c1ccccc1Oc1ccc(C(F)(F)F)cc1NS(=O)(=O)c1ccc(Cl)cc1 10.1016/j.bmcl.2010.04.142
CHEMBL1171586 25053 0 None None None Human 6.3 pKi = 6.3 Functional
Antagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrsAntagonist activity at human CCR1 assessed as inhibition of MIP-1-alpha-induced [35S]-GTPgammaS binding after 3 to 4 hrs
ChEMBL 471 6 2 4 5.7 O=C(O)c1ccccc1Oc1ccc(C(F)(F)F)cc1NS(=O)(=O)c1ccc(Cl)cc1 10.1016/j.bmcl.2010.04.142
15664 174775 66 None -3 3 Human 8.3 pEC50 = 8.3 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
Drug Central 184 1 0 2 2.8 Cc1ccc(-c2ccc(C)cn2)nc1 None
5403 174775 66 None -3 3 Human 8.3 pEC50 = 8.3 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
Drug Central 184 1 0 2 2.8 Cc1ccc(-c2ccc(C)cn2)nc1 None
CHEMBL2205807 174775 66 None -3 3 Human 8.3 pEC50 = 8.3 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
Drug Central 184 1 0 2 2.8 Cc1ccc(-c2ccc(C)cn2)nc1 None
DB11932 174775 66 None -3 3 Human 8.3 pEC50 = 8.3 Functional
Allosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysisAllosteric modulation at human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr assessed as {3H]IP3 turnover by liquid scintillation counting analysis
Drug Central 184 1 0 2 2.8 Cc1ccc(-c2ccc(C)cn2)nc1 None
3536 8490 0 None 9 2 Human 8.0 pIC50 = 8.0 Functional
Measuring antagonism of CCL3-induced chemotaxis <i>in vitro</i>.Measuring antagonism of CCL3-induced chemotaxis <i>in vitro</i>.
Guide to Pharmacology 515 5 1 2 7.3 CC[N+]1(CCC(CC1)NC(=O)C1c2cc(Cl)ccc2Oc2c1cc(Cl)cc2)CC1CCCCCC1 10854442
44560289 8490 0 None 9 2 Human 8.0 pIC50 = 8.0 Functional
Measuring antagonism of CCL3-induced chemotaxis <i>in vitro</i>.Measuring antagonism of CCL3-induced chemotaxis <i>in vitro</i>.
Guide to Pharmacology 515 5 1 2 7.3 CC[N+]1(CCC(CC1)NC(=O)C1c2cc(Cl)ccc2Oc2c1cc(Cl)cc2)CC1CCCCCC1 10854442
CHEMBL1186993 8490 0 None 9 2 Human 8.0 pIC50 = 8.0 Functional
Measuring antagonism of CCL3-induced chemotaxis <i>in vitro</i>.Measuring antagonism of CCL3-induced chemotaxis <i>in vitro</i>.
Guide to Pharmacology 515 5 1 2 7.3 CC[N+]1(CCC(CC1)NC(=O)C1c2cc(Cl)ccc2Oc2c1cc(Cl)cc2)CC1CCCCCC1 10854442
4382 1724 0 None -25 2 Human 6.1 pIC50 = 6.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23951310
P55774 1724 0 None -25 2 Human 6.1 pIC50 = 6.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23951310
754 1718 0 None -5 2 Human 7.9 pIC50 = 7.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9346309
Q16663 1718 0 None -5 2 Human 7.9 pIC50 = 7.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9346309
3696 2178 0 None None None Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology 584 6 2 5 6.0 NC[C@@H]1CCCN(C1)C(=O)c1ccc2c(c1)C(C(=O)NC1CCN(CC1)CC1=CCCCCCCC1)c1c(O2)cccc1 12614873
73755059 2178 0 None None None Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology 584 6 2 5 6.0 NC[C@@H]1CCCN(C1)C(=O)c1ccc2c(c1)C(C(=O)NC1CCN(CC1)CC1=CCCCCCCC1)c1c(O2)cccc1 12614873
10750 5246 0 None 5011 2 Human 9.1 pIC50 = 9.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 532 5 2 5 6.3 Clc1ccc(cc1)C1(O)CCN(CC1(C)C)CC/C=C\1/c2cc(ccc2OCc2c1cccn2)C(O)(C)C None
18437138 5246 0 None 5011 2 Human 9.1 pIC50 = 9.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 532 5 2 5 6.3 Clc1ccc(cc1)C1(O)CCN(CC1(C)C)CC/C=C\1/c2cc(ccc2OCc2c1cccn2)C(O)(C)C None
486830 8678 0 None -10 5 Human 8.1 pIC50 None 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 1308 22 19 19 -5.9 NCCCC[C@@H]1NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)CNC(=O)[C@@H](NC1=O)CCCN=C(N)N)CCCN=C(N)N)CCC(=O)N)C(C)C)C(=O)O)[C@H](O)C 9287217
768 8678 0 None -10 5 Human 8.1 pIC50 None 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 1308 22 19 19 -5.9 NCCCC[C@@H]1NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)CNC(=O)[C@@H](NC1=O)CCCN=C(N)N)CCCN=C(N)N)CCC(=O)N)C(C)C)C(=O)O)[C@H](O)C 9287217




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72548703 317107 0 None None None Human 10.1 pIC50 = 10.1 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 receptor after 120 mins by scintillation counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 receptor after 120 mins by scintillation counting analysis
ChEMBL 583 8 3 6 5.8 CC(C)(C)NS(=O)(=O)c1ccc(-c2sc(C(=O)N[C@H]3C[C@H](C(=O)O)C3)nc2CC2CCCCC2)c2ccccc12 10.1016/j.bmcl.2018.03.093
CHEMBL4128926 317107 0 None None None Human 10.1 pIC50 = 10.1 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 receptor after 120 mins by scintillation counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 receptor after 120 mins by scintillation counting analysis
ChEMBL 583 8 3 6 5.8 CC(C)(C)NS(=O)(=O)c1ccc(-c2sc(C(=O)N[C@H]3C[C@H](C(=O)O)C3)nc2CC2CCCCC2)c2ccccc12 10.1016/j.bmcl.2018.03.093
25109291 366002 9 None None None Human 10.1 pIC50 = 10.1 Binding
Displacement of radiolabeled MIP1alpha from human CCR1 receptorDisplacement of radiolabeled MIP1alpha from human CCR1 receptor
ChEMBL 327 1 2 6 1.7 Nc1nc2c(c(N3CCNCC3)n1)CCC1=C2[C@@H]2CCCC[C@@H]2O1 10.1021/jm8007618
CHEMBL519240 366002 9 None None None Human 10.1 pIC50 = 10.1 Binding
Displacement of radiolabeled MIP1alpha from human CCR1 receptorDisplacement of radiolabeled MIP1alpha from human CCR1 receptor
ChEMBL 327 1 2 6 1.7 Nc1nc2c(c(N3CCNCC3)n1)CCC1=C2[C@@H]2CCCC[C@@H]2O1 10.1021/jm8007618
59278286 336088 1 None None None Human 9.5 pIC50 = 9.5 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 453 6 1 7 3.2 CC[C@H](NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4464625 336088 1 None None None Human 9.5 pIC50 = 9.5 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 453 6 1 7 3.2 CC[C@H](NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
11744314 178226 0 None None None Human 9.4 pIC50 = 9.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 446 6 3 6 3.2 CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
CHEMBL2332935 178226 0 None None None Human 9.4 pIC50 = 9.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 446 6 3 6 3.2 CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
68959963 178224 0 None None None Human 9.4 pIC50 = 9.4 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 432 6 2 5 3.1 CC(=O)Nc1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2012.12.095
CHEMBL2332933 178224 0 None None None Human 9.4 pIC50 = 9.4 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 432 6 2 5 3.1 CC(=O)Nc1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2012.12.095
11744314 178226 0 None None None Human 9.4 pIC50 = 9.4 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 446 6 3 6 3.2 CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2012.12.095
CHEMBL2332935 178226 0 None None None Human 9.4 pIC50 = 9.4 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 446 6 3 6 3.2 CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2012.12.095
10094212 178227 0 None None None Human 9.3 pIC50 = 9.3 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 430 6 3 6 2.7 CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2013.04.047
CHEMBL2332936 178227 0 None None None Human 9.3 pIC50 = 9.3 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 430 6 3 6 2.7 CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2013.04.047
10094212 178227 0 None None None Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 430 6 3 6 2.7 CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2012.12.095
CHEMBL2332936 178227 0 None None None Human 9.3 pIC50 = 9.3 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 430 6 3 6 2.7 CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2012.12.095
72945512 214044 0 None None None Human 9.2 pIC50 = 9.2 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 471 7 4 6 3.0 O=C(Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2)NC1CC1 10.1016/j.bmcl.2013.11.062
CHEMBL3099947 214044 0 None None None Human 9.2 pIC50 = 9.2 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 471 7 4 6 3.0 O=C(Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2)NC1CC1 10.1016/j.bmcl.2013.11.062
10478859 178222 0 None None None Human 9.2 pIC50 = 9.2 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 448 6 2 5 3.6 CC(=O)Nc1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2012.12.095
CHEMBL2332931 178222 0 None None None Human 9.2 pIC50 = 9.2 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 448 6 2 5 3.6 CC(=O)Nc1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2012.12.095
25141109 258188 0 None None None Human 9.2 pIC50 = 9.2 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 493 5 4 4 3.8 C[C@H](NC(=O)N[C@@H]1CCCC[C@@H]1C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)(C)O nan
CHEMBL3679659 258188 0 None None None Human 9.2 pIC50 = 9.2 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 493 5 4 4 3.8 C[C@H](NC(=O)N[C@@H]1CCCC[C@@H]1C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)(C)O nan
71570633 178231 0 None None None Human 9.1 pIC50 = 9.1 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 445 6 3 6 3.2 CC(=O)Nc1ccc(O)cc1OC[C@@H](N)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2012.12.095
CHEMBL2332940 178231 0 None None None Human 9.1 pIC50 = 9.1 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 445 6 3 6 3.2 CC(=O)Nc1ccc(O)cc1OC[C@@H](N)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2012.12.095
21070989 177765 0 None None None Human 9.1 pIC50 = 9.1 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL5/RANTES-induced chemotaxisAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL5/RANTES-induced chemotaxis
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None None None Human 9.1 pIC50 = 9.1 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL5/RANTES-induced chemotaxisAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL5/RANTES-induced chemotaxis
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
57889003 181969 9 None None None Human 9.1 pIC50 = 9.1 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889430 181969 9 None None None Human 9.1 pIC50 = 9.1 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398726 181969 9 None None None Human 9.1 pIC50 = 9.1 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398728 181969 9 None None None Human 9.1 pIC50 = 9.1 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57888919 181970 0 None None None Human 9.1 pIC50 = 9.1 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889974 181970 0 None None None Human 9.1 pIC50 = 9.1 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398727 181970 0 None None None Human 9.1 pIC50 = 9.1 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398729 181970 0 None None None Human 9.1 pIC50 = 9.1 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
72945510 214042 0 None None None Human 9.1 pIC50 = 9.1 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 487 7 4 6 3.5 O=C(Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)NC1CC1 10.1016/j.bmcl.2013.11.062
CHEMBL3099945 214042 0 None None None Human 9.1 pIC50 = 9.1 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 487 7 4 6 3.5 O=C(Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)NC1CC1 10.1016/j.bmcl.2013.11.062
6918497 232475 1 None None None Human 9.1 pIC50 = 9.1 Binding
Binding affinity towards C-C chemokine receptor type 1Binding affinity towards C-C chemokine receptor type 1
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1016/s0960-894x(03)00748-0
CHEMBL331897 232475 1 None None None Human 9.1 pIC50 = 9.1 Binding
Binding affinity towards C-C chemokine receptor type 1Binding affinity towards C-C chemokine receptor type 1
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1016/s0960-894x(03)00748-0
6918497 232475 1 None None None Human 9.1 pIC50 = 9.1 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1016/s0960-894x(01)00176-7
CHEMBL331897 232475 1 None None None Human 9.1 pIC50 = 9.1 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1016/s0960-894x(01)00176-7
10389562 178221 0 None None None Human 9.1 pIC50 = 9.1 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 460 7 2 6 3.5 COc1ccc(NC(C)=O)c(OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)c1 10.1016/j.bmcl.2012.12.095
CHEMBL2332930 178221 0 None None None Human 9.1 pIC50 = 9.1 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 460 7 2 6 3.5 COc1ccc(NC(C)=O)c(OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)c1 10.1016/j.bmcl.2012.12.095
6918497 232475 1 None None None Human 9.1 pIC50 = 9.1 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
CHEMBL331897 232475 1 None None None Human 9.1 pIC50 = 9.1 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
10032207 181601 0 None None None Human 9.0 pIC50 = 9.0 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 536 6 3 7 3.1 O=C(c1cc(Cl)c(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CC[C@H](O)C1 10.1016/j.bmcl.2013.04.047
CHEMBL2391803 181601 0 None None None Human 9.0 pIC50 = 9.0 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 536 6 3 7 3.1 O=C(c1cc(Cl)c(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CC[C@H](O)C1 10.1016/j.bmcl.2013.04.047
9954423 178223 0 None None None Human 9.0 pIC50 = 9.0 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 430 6 2 5 3.5 CC(=O)Nc1ccccc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2012.12.095
CHEMBL2332932 178223 0 None None None Human 9.0 pIC50 = 9.0 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 430 6 2 5 3.5 CC(=O)Nc1ccccc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2012.12.095
10409538 178225 0 None None None Human 9.0 pIC50 = 9.0 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 414 6 2 5 3.0 CC(=O)Nc1ccccc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2012.12.095
CHEMBL2332934 178225 0 None None None Human 9.0 pIC50 = 9.0 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 414 6 2 5 3.0 CC(=O)Nc1ccccc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2012.12.095
57889003 181969 9 None None None Human 9.0 pIC50 = 9 Binding
Antagonist activity at human CCR1 assessed as inhibition of RANTES-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of RANTES-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889430 181969 9 None None None Human 9.0 pIC50 = 9 Binding
Antagonist activity at human CCR1 assessed as inhibition of RANTES-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of RANTES-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398726 181969 9 None None None Human 9.0 pIC50 = 9 Binding
Antagonist activity at human CCR1 assessed as inhibition of RANTES-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of RANTES-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398728 181969 9 None None None Human 9.0 pIC50 = 9 Binding
Antagonist activity at human CCR1 assessed as inhibition of RANTES-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of RANTES-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889327 181961 0 None None None Human 9.0 pIC50 = 9 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 420 6 2 3 3.7 CC(C)[C@@H](NC(=O)CC1CC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398717 181961 0 None None None Human 9.0 pIC50 = 9 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 420 6 2 3 3.7 CC(C)[C@@H](NC(=O)CC1CC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
44537841 1390 22 None None None Human 9.0 pIC50 = 9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 9.0 pIC50 = 9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 9.0 pIC50 = 9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 9.0 pIC50 = 9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 9.0 pIC50 = 9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57888993 233485 0 None None None Human 9.0 pIC50 = 9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 471 6 3 3 4.3 CC(C)[C@@H](NC(=O)NCc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334818 233485 0 None None None Human 9.0 pIC50 = 9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 471 6 3 3 4.3 CC(C)[C@@H](NC(=O)NCc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
59278286 336088 1 None None None Human 9.0 pIC50 = 9 Binding
Inhibition of MIP1alpha-stimulated CCR1 internalization in human whole blood preincubated for 30 mins followed by MIP1alpha-stimulation and measured after 40 mins by Alexa647 staining based FACS analysisInhibition of MIP1alpha-stimulated CCR1 internalization in human whole blood preincubated for 30 mins followed by MIP1alpha-stimulation and measured after 40 mins by Alexa647 staining based FACS analysis
ChEMBL 453 6 1 7 3.2 CC[C@H](NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
CHEMBL4464625 336088 1 None None None Human 9.0 pIC50 = 9 Binding
Inhibition of MIP1alpha-stimulated CCR1 internalization in human whole blood preincubated for 30 mins followed by MIP1alpha-stimulation and measured after 40 mins by Alexa647 staining based FACS analysisInhibition of MIP1alpha-stimulated CCR1 internalization in human whole blood preincubated for 30 mins followed by MIP1alpha-stimulation and measured after 40 mins by Alexa647 staining based FACS analysis
ChEMBL 453 6 1 7 3.2 CC[C@H](NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(S(C)(=O)=O)c1 10.1016/j.bmcl.2018.12.024
25175119 258180 0 None None None Human 9.0 pIC50 = 9 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 533 5 3 5 3.0 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)c2cccc(S(N)(=O)=O)c2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679651 258180 0 None None None Human 9.0 pIC50 = 9 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 533 5 3 5 3.0 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)c2cccc(S(N)(=O)=O)c2)CC[C@]1(O)c1ccc(Cl)cc1 nan
68963686 181608 0 None None None Human 9.0 pIC50 = 9.0 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 516 6 3 7 2.9 O=C(c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CCC(O)CC1 10.1016/j.bmcl.2013.04.047
CHEMBL2391810 181608 0 None None None Human 9.0 pIC50 = 9.0 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 516 6 3 7 2.9 O=C(c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CCC(O)CC1 10.1016/j.bmcl.2013.04.047
512282 1562 44 None None None Human 9.0 pIC50 = 9.0 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2018.11.015
767 1562 44 None None None Human 9.0 pIC50 = 9.0 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2018.11.015
CHEMBL232656 1562 44 None None None Human 9.0 pIC50 = 9.0 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2018.11.015
57889003 181969 9 None None None Human 9.0 pIC50 = 9.0 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889430 181969 9 None None None Human 9.0 pIC50 = 9.0 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398726 181969 9 None None None Human 9.0 pIC50 = 9.0 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398728 181969 9 None None None Human 9.0 pIC50 = 9.0 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57888834 181985 0 None None None Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 436 7 2 3 4.4 CC(C)CCC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL2398744 181985 0 None None None Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 436 7 2 3 4.4 CC(C)CCC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
57889764 182007 0 None None None Human 8.9 pIC50 = 8.9 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 457 6 2 4 3.6 CC(C)[C@@H](NC(=O)Cc1ccncc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398769 182007 0 None None None Human 8.9 pIC50 = 8.9 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 457 6 2 4 3.6 CC(C)[C@@H](NC(=O)Cc1ccncc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
6918497 232475 1 None None None Human 8.9 pIC50 = 8.9 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1016/j.ejmech.2020.113085
CHEMBL331897 232475 1 None None None Human 8.9 pIC50 = 8.9 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1016/j.ejmech.2020.113085
6918497 232475 1 None None None Human 8.9 pIC50 = 8.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
CHEMBL331897 232475 1 None None None Human 8.9 pIC50 = 8.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
71655299 181595 0 None None None Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 529 7 2 7 3.0 CN(C)[C@@H]1CCN(C(=O)c2ccc(O)cc2OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)C1 10.1016/j.bmcl.2013.04.047
CHEMBL2391797 181595 0 None None None Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 529 7 2 7 3.0 CN(C)[C@@H]1CCN(C(=O)c2ccc(O)cc2OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)C1 10.1016/j.bmcl.2013.04.047
72945311 214039 0 None None None Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 461 6 4 6 3.0 CNC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.11.062
CHEMBL3099942 214039 0 None None None Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 461 6 4 6 3.0 CNC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.11.062
25175289 258184 0 None None None Human 8.9 pIC50 = 8.9 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 446 4 2 3 4.3 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)C2CCCC2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679655 258184 0 None None None Human 8.9 pIC50 = 8.9 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 446 4 2 3 4.3 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)C2CCCC2)CC[C@]1(O)c1ccc(Cl)cc1 nan
10367570 181593 0 None None None Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 472 7 3 6 3.1 O=C(NC1CC1)c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
CHEMBL2391795 181593 0 None None None Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 472 7 3 6 3.1 O=C(NC1CC1)c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
10412648 181632 0 None None None Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 474 7 2 5 3.6 O=C(NC1CC1)c1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
CHEMBL2391939 181632 0 None None None Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 474 7 2 5 3.6 O=C(NC1CC1)c1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
57889423 181988 0 None None None Human 8.9 pIC50 = 8.9 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 434 5 2 3 4.1 CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398747 181988 0 None None None Human 8.9 pIC50 = 8.9 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 434 5 2 3 4.1 CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
68959770 214037 0 None None None Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 485 6 2 5 4.2 O=C(Nc1ccccc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CCCC1 10.1016/j.bmcl.2013.11.062
CHEMBL3099940 214037 0 None None None Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 485 6 2 5 4.2 O=C(Nc1ccccc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CCCC1 10.1016/j.bmcl.2013.11.062
42602331 178232 0 None None None Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 429 6 3 6 2.7 CC(=O)Nc1ccc(O)cc1OC[C@@H](N)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2012.12.095
CHEMBL2332941 178232 0 None None None Human 8.9 pIC50 = 8.9 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 429 6 3 6 2.7 CC(=O)Nc1ccc(O)cc1OC[C@@H](N)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2012.12.095
21070989 177765 0 None None None Human 8.8 pIC50 = 8.8 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL15/Leukotactin1-induced chemotaxisAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL15/Leukotactin1-induced chemotaxis
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None None None Human 8.8 pIC50 = 8.8 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL15/Leukotactin1-induced chemotaxisAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL15/Leukotactin1-induced chemotaxis
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
44537841 1390 22 None None None Human 8.8 pIC50 = 8.8 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2018.11.015
57889181 1390 22 None None None Human 8.8 pIC50 = 8.8 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2018.11.015
9497 1390 22 None None None Human 8.8 pIC50 = 8.8 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2018.11.015
CHEMBL2398716 1390 22 None None None Human 8.8 pIC50 = 8.8 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2018.11.015
CHEMBL3334824 1390 22 None None None Human 8.8 pIC50 = 8.8 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2018.11.015
25141158 350212 0 None None None Human 8.8 pIC50 = 8.8 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 471 5 2 4 4.4 Cc1cc(C)c(C(=O)NC(C)(C)CC(=O)N2CC[C@](O)(c3ccc(Cl)cc3)C(C)(C)C2)cn1 nan
CHEMBL4594791 350212 0 None None None Human 8.8 pIC50 = 8.8 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 471 5 2 4 4.4 Cc1cc(C)c(C(=O)NC(C)(C)CC(=O)N2CC[C@](O)(c3ccc(Cl)cc3)C(C)(C)C2)cn1 nan
25175123 258182 0 None None None Human 8.8 pIC50 = 8.8 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 462 4 3 4 3.2 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)[C@H]2CC[C@@H](O)C2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679653 258182 0 None None None Human 8.8 pIC50 = 8.8 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 462 4 3 4 3.2 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)[C@H]2CC[C@@H](O)C2)CC[C@]1(O)c1ccc(Cl)cc1 nan
57889003 181969 9 None None None Human 8.8 pIC50 = 8.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889430 181969 9 None None None Human 8.8 pIC50 = 8.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398726 181969 9 None None None Human 8.8 pIC50 = 8.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398728 181969 9 None None None Human 8.8 pIC50 = 8.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
25175288 258183 0 None None None Human 8.8 pIC50 = 8.8 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 498 5 3 4 4.1 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)c2cccc(C(=O)O)c2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679654 258183 0 None None None Human 8.8 pIC50 = 8.8 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 498 5 3 4 4.1 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)c2cccc(C(=O)O)c2)CC[C@]1(O)c1ccc(Cl)cc1 nan
57889230 181980 0 None None None Human 8.8 pIC50 = 8.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 484 8 2 3 5.0 CC(C)[C@@H](NC(=O)CCCc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398739 181980 0 None None None Human 8.8 pIC50 = 8.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 484 8 2 3 5.0 CC(C)[C@@H](NC(=O)CCCc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57888834 181985 0 None None None Human 8.8 pIC50 = 8.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 436 7 2 3 4.4 CC(C)CCC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL2398744 181985 0 None None None Human 8.8 pIC50 = 8.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 436 7 2 3 4.4 CC(C)CCC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
25206951 349344 0 None None None Human 8.8 pIC50 = 8.8 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 434 5 2 3 4.3 CC(C)(CC(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)NC(=O)C1CCCC1 nan
CHEMBL4574123 349344 0 None None None Human 8.8 pIC50 = 8.8 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 434 5 2 3 4.3 CC(C)(CC(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)NC(=O)C1CCCC1 nan
42602328 181591 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 446 6 3 6 2.6 CNC(=O)c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
CHEMBL2391793 181591 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 446 6 3 6 2.6 CNC(=O)c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
10368175 181606 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 486 6 2 6 3.5 O=C(c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CCCC1 10.1016/j.bmcl.2013.04.047
CHEMBL2391808 181606 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 486 6 2 6 3.5 O=C(c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CCCC1 10.1016/j.bmcl.2013.04.047
66686405 346689 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 532 5 2 5 6.3 CC(C)(O)c1ccc2c(c1)/C(=C\CCN1CC[C@](O)(c3ccc(Cl)cc3)C(C)(C)C1)c1cccnc1CO2 10.1016/j.bmcl.2018.11.015
CHEMBL4571977 346689 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 532 5 2 5 6.3 CC(C)(O)c1ccc2c(c1)/C(=C\CCN1CC[C@](O)(c3ccc(Cl)cc3)C(C)(C)C1)c1cccnc1CO2 10.1016/j.bmcl.2018.11.015
57889897 181978 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 456 6 2 3 4.2 CC(C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398737 181978 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 456 6 2 3 4.2 CC(C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889071 181987 0 None None None Human 8.7 pIC50 = 8.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 420 5 2 3 3.7 CC(C)[C@@H](NC(=O)C1CCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398746 181987 0 None None None Human 8.7 pIC50 = 8.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 420 5 2 3 3.7 CC(C)[C@@H](NC(=O)C1CCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
59444283 336906 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 485 6 3 4 3.5 CC(C)(CC(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)NC(=O)c1cccc(C(N)=O)c1 nan
CHEMBL4476397 336906 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 485 6 3 4 3.5 CC(C)(CC(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)NC(=O)c1cccc(C(N)=O)c1 nan
72945313 214040 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 521 7 4 6 4.2 O=C(Nc1cc(Cl)c(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)NC1CC1 10.1016/j.bmcl.2013.11.062
CHEMBL3099943 214040 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 521 7 4 6 4.2 O=C(Nc1cc(Cl)c(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)NC1CC1 10.1016/j.bmcl.2013.11.062
72945314 214041 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 501 8 3 6 3.8 COc1ccc(NC(=O)NC2CC2)c(OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)c1 10.1016/j.bmcl.2013.11.062
CHEMBL3099944 214041 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 501 8 3 6 3.8 COc1ccc(NC(=O)NC2CC2)c(OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)c1 10.1016/j.bmcl.2013.11.062
59474992 258185 0 None None None Human 8.7 pIC50 = 8.7 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 497 5 3 4 3.5 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)c2cccc(C(N)=O)c2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679656 258185 0 None None None Human 8.7 pIC50 = 8.7 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 497 5 3 4 3.5 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)c2cccc(C(N)=O)c2)CC[C@]1(O)c1ccc(Cl)cc1 nan
10436125 181602 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 502 6 3 7 2.5 O=C(c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CC[C@H](O)C1 10.1016/j.bmcl.2013.04.047
CHEMBL2391804 181602 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 502 6 3 7 2.5 O=C(c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CC[C@H](O)C1 10.1016/j.bmcl.2013.04.047
57889334 181984 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 422 6 2 3 4.0 CC(C)CC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL2398743 181984 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 422 6 2 3 4.0 CC(C)CC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
59444225 336208 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 467 6 4 4 3.4 C[C@H](NC(=O)NC(C)(C)CC(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)(C)O nan
CHEMBL4466344 336208 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 467 6 4 4 3.4 C[C@H](NC(=O)NC(C)(C)CC(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)(C)O nan
11803142 26286 0 None None None Human 8.7 pIC50 = 8.7 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 615 5 1 2 7.8 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
CHEMBL1183314 26286 0 None None None Human 8.7 pIC50 = 8.7 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 615 5 1 2 7.8 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
57889736 233480 0 None None None Human 8.0 pIC50 = 8 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334727 233480 0 None None None Human 8.0 pIC50 = 8 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
57889679 181999 0 None None None Human 8.0 pIC50 = 8 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 442 5 2 3 4.2 CC(C)[C@@H](NC(=O)c1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398761 181999 0 None None None Human 8.0 pIC50 = 8 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 442 5 2 3 4.2 CC(C)[C@@H](NC(=O)c1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57888966 182009 0 None None None Human 8.0 pIC50 = 8 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1cccc(Cl)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398771 182009 0 None None None Human 8.0 pIC50 = 8 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1cccc(Cl)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889613 182000 0 None None None Human 8.0 pIC50 = 8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 432 5 2 3 4.3 CC(C)[C@@H](NC(=O)c1ccc(F)c(O)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2398762 182000 0 None None None Human 8.0 pIC50 = 8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 432 5 2 3 4.3 CC(C)[C@@H](NC(=O)c1ccc(F)c(O)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
57840192 177673 0 None None None Human 8.0 pIC50 = 8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 460 5 0 7 2.3 COc1cc(N2CCN(C(=O)Cn3nc(S(C)(=O)=O)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2321887 177673 0 None None None Human 8.0 pIC50 = 8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 460 5 0 7 2.3 COc1cc(N2CCN(C(=O)Cn3nc(S(C)(=O)=O)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
57840295 177735 0 None None None Human 8.0 pIC50 = 8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 407 4 0 6 2.7 COc1cc(N2CCN(C(=O)Cn3nc(C#N)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322847 177735 0 None None None Human 8.0 pIC50 = 8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 407 4 0 6 2.7 COc1cc(N2CCN(C(=O)Cn3nc(C#N)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
57840511 177757 0 None None None Human 8.0 pIC50 = 8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 466 5 1 6 3.1 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3CO)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322867 177757 0 None None None Human 8.0 pIC50 = 8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 466 5 1 6 3.1 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3CO)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
71719855 177770 0 None None None Human 8.0 pIC50 = 8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 484 4 0 5 4.5 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(Cl)c1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322880 177770 0 None None None Human 8.0 pIC50 = 8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 484 4 0 5 4.5 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(Cl)c1Cl 10.1016/j.bmcl.2013.01.005
17753030 177887 0 None None None Human 8.0 pIC50 = 8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 486 7 2 7 2.5 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(N)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232441 177887 0 None None None Human 8.0 pIC50 = 8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 486 7 2 7 2.5 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(N)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
59278314 334482 29 None None None Human 8.0 pIC50 = 8 Binding
Inhibition of MIP1alpha-stimulated CCR1 internalization in human whole blood preincubated for 30 mins followed by MIP1alpha-stimulation and measured after 40 mins by Alexa647 staining based FACS analysisInhibition of MIP1alpha-stimulated CCR1 internalization in human whole blood preincubated for 30 mins followed by MIP1alpha-stimulation and measured after 40 mins by Alexa647 staining based FACS analysis
ChEMBL 425 5 1 7 2.3 CS(=O)(=O)c1cc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)ccn1 10.1016/j.bmcl.2018.12.024
CHEMBL4441094 334482 29 None None None Human 8.0 pIC50 = 8 Binding
Inhibition of MIP1alpha-stimulated CCR1 internalization in human whole blood preincubated for 30 mins followed by MIP1alpha-stimulation and measured after 40 mins by Alexa647 staining based FACS analysisInhibition of MIP1alpha-stimulated CCR1 internalization in human whole blood preincubated for 30 mins followed by MIP1alpha-stimulation and measured after 40 mins by Alexa647 staining based FACS analysis
ChEMBL 425 5 1 7 2.3 CS(=O)(=O)c1cc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)ccn1 10.1016/j.bmcl.2018.12.024
512282 1562 44 None None None Human 8.0 pIC50 = 8 Binding
Inhibition of human recombinant CCR1Inhibition of human recombinant CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/acs.jmedchem.6b01309
767 1562 44 None None None Human 8.0 pIC50 = 8 Binding
Inhibition of human recombinant CCR1Inhibition of human recombinant CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/acs.jmedchem.6b01309
CHEMBL232656 1562 44 None None None Human 8.0 pIC50 = 8 Binding
Inhibition of human recombinant CCR1Inhibition of human recombinant CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/acs.jmedchem.6b01309
512282 1562 44 None None None Human 8.0 pIC50 = 8 Binding
Inhibition of human wild type CCR1Inhibition of human wild type CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/acs.jmedchem.6b01309
767 1562 44 None None None Human 8.0 pIC50 = 8 Binding
Inhibition of human wild type CCR1Inhibition of human wild type CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/acs.jmedchem.6b01309
CHEMBL232656 1562 44 None None None Human 8.0 pIC50 = 8 Binding
Inhibition of human wild type CCR1Inhibition of human wild type CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/acs.jmedchem.6b01309
21070993 177764 0 None None None Human 7.0 pIC50 = 7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 434 3 0 4 4.2 Cc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322874 177764 0 None None None Human 7.0 pIC50 = 7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 434 3 0 4 4.2 Cc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
57888715 164267 0 None None None Human 7.0 pIC50 = 7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 5 1 2 5.1 Cc1cccc(C(=O)N[C@@H](C(=O)N2CCC(c3ccc(Cl)cc3)CC2)C(C)C)c1C 10.1021/jm300896d
CHEMBL2180511 164267 0 None None None Human 7.0 pIC50 = 7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 5 1 2 5.1 Cc1cccc(C(=O)N[C@@H](C(=O)N2CCC(c3ccc(Cl)cc3)CC2)C(C)C)c1C 10.1021/jm300896d
44430755 309540 0 None None None Mouse 6.0 pIC50 = 6 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 577 10 2 8 3.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2cccnc2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL397910 309540 0 None None None Mouse 6.0 pIC50 = 6 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 577 10 2 8 3.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2cccnc2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453527 197842 0 None None None Human 6.0 pIC50 = 6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 477 4 0 4 4.7 N#CC1(c2ccc(Cl)cc2)CCN(C2CCN(S(=O)(=O)c3ccccc3Cl)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL270563 197842 0 None None None Human 6.0 pIC50 = 6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 477 4 0 4 4.7 N#CC1(c2ccc(Cl)cc2)CCN(C2CCN(S(=O)(=O)c3ccccc3Cl)CC2)CC1 10.1016/j.bmcl.2007.09.068
5481702 470631 0 None None None Human 5.0 pIC50 = 5 Binding
Compound concentration that causes 50 % inhibition of binding of specific radioligand to human CCR1 receptorCompound concentration that causes 50 % inhibition of binding of specific radioligand to human CCR1 receptor
ChEMBL 556 8 0 4 5.3 CN(C[C@@H](CCN1CCC2(CC1)C[S+]([O-])c1ccccc12)c1cccc(Cl)c1)S(=O)(=O)c1ccccc1 10.1016/s0960-894x(00)00639-9
CHEMBL83338 470631 0 None None None Human 5.0 pIC50 = 5 Binding
Compound concentration that causes 50 % inhibition of binding of specific radioligand to human CCR1 receptorCompound concentration that causes 50 % inhibition of binding of specific radioligand to human CCR1 receptor
ChEMBL 556 8 0 4 5.3 CN(C[C@@H](CCN1CCC2(CC1)C[S+]([O-])c1ccccc12)c1cccc(Cl)c1)S(=O)(=O)c1ccccc1 10.1016/s0960-894x(00)00639-9
11329244 143347 6 None None None Human 5.0 pIC50 = 5 Binding
Inhibition of C-C chemokine receptor type 1Inhibition of C-C chemokine receptor type 1
ChEMBL 486 7 2 5 5.4 CC(=O)c1sc(NC(=O)N[C@@H]2CCCC[C@H]2CN2CCC[C@@H](Cc3ccc(F)cc3)C2)nc1C 10.1021/jm049530m
CHEMBL195433 143347 6 None None None Human 5.0 pIC50 = 5 Binding
Inhibition of C-C chemokine receptor type 1Inhibition of C-C chemokine receptor type 1
ChEMBL 486 7 2 5 5.4 CC(=O)c1sc(NC(=O)N[C@@H]2CCCC[C@H]2CN2CCC[C@@H](Cc3ccc(F)cc3)C2)nc1C 10.1021/jm049530m
11272103 252399 0 None None None Human 5.0 pIC50 = 5 Binding
Inhibition of C-C chemokine receptor type 1Inhibition of C-C chemokine receptor type 1
ChEMBL 505 7 2 6 4.7 Cn1nnnc1-c1cccc(NC(=O)N[C@@H]2CCCC[C@H]2CN2CCC[C@@H](Cc3ccc(F)cc3)C2)c1 10.1021/jm049530m
CHEMBL363840 252399 0 None None None Human 5.0 pIC50 = 5 Binding
Inhibition of C-C chemokine receptor type 1Inhibition of C-C chemokine receptor type 1
ChEMBL 505 7 2 6 4.7 Cn1nnnc1-c1cccc(NC(=O)N[C@@H]2CCCC[C@H]2CN2CCC[C@@H](Cc3ccc(F)cc3)C2)c1 10.1021/jm049530m
14338 18716 77 None None None Human 4.0 pIC50 = 4 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 184 1 0 2 2.8 Cc1ccnc(-c2cc(C)ccn2)c1 10.1021/jm301121j
CHEMBL101165 18716 77 None None None Human 4.0 pIC50 = 4 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 184 1 0 2 2.8 Cc1ccnc(-c2cc(C)ccn2)c1 10.1021/jm301121j
72792 433102 57 None None None Human 4.0 pIC50 = 4 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 208 0 0 2 3.4 Cc1ccnc2c1ccc1c(C)ccnc12 10.1021/jm301121j
CHEMBL593442 433102 57 None None None Human 4.0 pIC50 = 4 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 208 0 0 2 3.4 Cc1ccnc2c1ccc1c(C)ccnc12 10.1021/jm301121j
DB02586 433102 57 None None None Human 4.0 pIC50 = 4 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 208 0 0 2 3.4 Cc1ccnc2c1ccc1c(C)ccnc12 10.1021/jm301121j
44309060 203039 0 None None None Human 5.0 pIC50 = 5.0 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 446 10 3 3 4.3 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccc2ccccc2c1 10.1016/j.bmcl.2004.02.021
CHEMBL306683 203039 0 None None None Human 5.0 pIC50 = 5.0 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 446 10 3 3 4.3 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccc2ccccc2c1 10.1016/j.bmcl.2004.02.021
57889664 164221 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 440 7 1 2 5.1 Cc1ccc(CCC(=O)N[C@@H](C(=O)N2CCC(c3ccc(Cl)cc3)CC2)C(C)C)cc1 10.1021/jm300896d
CHEMBL2180194 164221 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 440 7 1 2 5.1 Cc1ccc(CCC(=O)N[C@@H](C(=O)N2CCC(c3ccc(Cl)cc3)CC2)C(C)C)cc1 10.1021/jm300896d
25175449 258170 0 None None None Human 6.0 pIC50 = 6.0 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 526 4 2 5 4.1 CC1(C)CN(C(=O)[C@H]2CC3(CC[C@H]2NC(=O)c2ccccc2)OCCO3)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679640 258170 0 None None None Human 6.0 pIC50 = 6.0 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 526 4 2 5 4.1 CC1(C)CN(C(=O)[C@H]2CC3(CC[C@H]2NC(=O)c2ccccc2)OCCO3)CC[C@]1(O)c1ccc(Cl)cc1 nan
57888707 182006 0 None None None Human 7.0 pIC50 = 7.0 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 413 6 1 3 3.8 CC(C)[C@@H](NC(=O)Cc1ccncc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2398768 182006 0 None None None Human 7.0 pIC50 = 7.0 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 413 6 1 3 3.8 CC(C)[C@@H](NC(=O)Cc1ccncc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
71718646 177768 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 4 0 5 4.2 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(C)c1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322878 177768 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 4 0 5 4.2 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(C)c1Cl 10.1016/j.bmcl.2013.01.005
57888718 164272 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 428 6 1 3 5.0 CC(C)C(NC(=O)OCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180518 164272 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 428 6 1 3 5.0 CC(C)C(NC(=O)OCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
71719253 177743 0 None None None Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 480 5 1 6 3.2 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)[C@H](CO)C2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322854 177743 0 None None None Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 480 5 1 6 3.2 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)[C@H](CO)C2)ccc1Cl 10.1016/j.bmcl.2013.01.005
25233756 354749 0 None None None Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 467 4 1 2 5.6 Cc1cc(C(F)(F)F)cc(C)c1NC(=O)N1CCC[C@@H]1C(=O)N(C)Cc1ccc(Cl)cc1 10.1021/jm801416q
CHEMBL475748 354749 0 None None None Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 467 4 1 2 5.6 Cc1cc(C(F)(F)F)cc(C)c1NC(=O)N1CCC[C@@H]1C(=O)N(C)Cc1ccc(Cl)cc1 10.1021/jm801416q
118714034 233487 0 None None None Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 424 6 3 4 2.7 CC(C)[C@@H](NC(=O)C[C@H](C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334820 233487 0 None None None Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 424 6 3 4 2.7 CC(C)[C@@H](NC(=O)C[C@H](C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
59474993 258186 0 None None None Human 8.0 pIC50 = 8.0 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 503 5 3 4 4.4 [C-]#[N+]c1ccc([C@@]2(O)CCN(C(=O)[C@H]3CCCC[C@H]3NC(=O)c3cccc(C(=O)O)c3)CC2(C)C)cc1 nan
CHEMBL3679657 258186 0 None None None Human 8.0 pIC50 = 8.0 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 503 5 3 4 4.4 [C-]#[N+]c1ccc([C@@]2(O)CCN(C(=O)[C@H]3CCCC[C@H]3NC(=O)c3cccc(C(=O)O)c3)CC2(C)C)cc1 nan
25175448 258168 0 None None None Human 7.9 pIC50 = 7.9 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 469 4 3 3 4.8 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)Nc2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679639 258168 0 None None None Human 7.9 pIC50 = 7.9 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 469 4 3 3 4.8 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)Nc2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
71655559 181603 0 None None None Human 7.0 pIC50 = 7.0 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 529 7 2 7 3.0 CN(C)[C@H]1CCN(C(=O)c2ccc(O)cc2OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)C1 10.1016/j.bmcl.2013.04.047
CHEMBL2391805 181603 0 None None None Human 7.0 pIC50 = 7.0 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 529 7 2 7 3.0 CN(C)[C@H]1CCN(C(=O)c2ccc(O)cc2OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)C1 10.1016/j.bmcl.2013.04.047
44453291 197729 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 442 7 2 4 3.6 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL269957 197729 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 442 7 2 4 3.6 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1Cl 10.1016/j.bmcl.2007.09.068
21071070 177755 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 478 5 0 5 4.7 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C(C)C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322865 177755 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 478 5 0 5 4.7 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C(C)C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
10811980 200129 0 None None None Human 6.0 pIC50 = 6.0 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 418 6 1 2 5.8 O=C(NC1CCN(CC2CCCCCCC2)CC1)C(c1ccccc1)c1ccccc1 10.1021/jm0004244
CHEMBL286355 200129 0 None None None Human 6.0 pIC50 = 6.0 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 418 6 1 2 5.8 O=C(NC1CCN(CC2CCCCCCC2)CC1)C(c1ccccc1)c1ccccc1 10.1021/jm0004244
21071081 177763 1 None None None Human 5.0 pIC50 = 5.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 420 3 0 4 3.9 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2cccc(Cl)c2)CC1 10.1016/j.bmcl.2013.01.005
CHEMBL2322873 177763 1 None None None Human 5.0 pIC50 = 5.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 420 3 0 4 3.9 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2cccc(Cl)c2)CC1 10.1016/j.bmcl.2013.01.005
44453227 195768 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 548 4 1 4 4.5 O=S(=O)(c1c(F)cc(F)cc1Br)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL256887 195768 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 548 4 1 4 4.5 O=S(=O)(c1c(F)cc(F)cc1Br)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
57888832 164215 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 446 6 1 2 5.1 CC(C)[C@@H](NC(=O)Cc1ccc(Cl)cc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180188 164215 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 446 6 1 2 5.1 CC(C)[C@@H](NC(=O)Cc1ccc(Cl)cc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44453436 197950 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 458 7 2 4 4.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc2ccccc2c1 10.1016/j.bmcl.2007.09.068
CHEMBL271079 197950 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 458 7 2 4 4.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc2ccccc2c1 10.1016/j.bmcl.2007.09.068
44453525 197806 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 452 4 1 4 3.6 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(F)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL270358 197806 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 452 4 1 4 3.6 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(F)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
24758046 164263 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 416 5 1 2 4.6 CC(C)[C@@H](NC(=O)c1ccc(F)cc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180507 164263 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 416 5 1 2 4.6 CC(C)[C@@H](NC(=O)c1ccc(F)cc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
12015739 213342 0 None None None Human 4.9 pIC50 = 4.9 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 413 10 3 4 3.5 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](CC(C)C)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
CHEMBL308690 213342 0 None None None Human 4.9 pIC50 = 4.9 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 413 10 3 4 3.5 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](CC(C)C)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
59444213 335839 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 484 5 2 4 4.2 CC1(C)CN(C(=O)CC2(NC(=O)c3ccccc3)CCOCC2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL4460796 335839 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 484 5 2 4 4.2 CC1(C)CN(C(=O)CC2(NC(=O)c3ccccc3)CCOCC2)CC[C@]1(O)c1ccc(Cl)cc1 nan
59444196 349306 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 442 5 2 3 4.2 CC(NC(=O)c1ccccc1)C(C)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
CHEMBL4573109 349306 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 442 5 2 3 4.2 CC(NC(=O)c1ccccc1)C(C)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
68963562 181600 0 None None None Human 7.9 pIC50 = 7.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 488 6 2 6 2.4 O=C(c1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2)N1CC[C@H](O)C1 10.1016/j.bmcl.2013.04.047
CHEMBL2391802 181600 0 None None None Human 7.9 pIC50 = 7.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 488 6 2 6 2.4 O=C(c1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2)N1CC[C@H](O)C1 10.1016/j.bmcl.2013.04.047
10073725 181610 0 None None None Human 7.9 pIC50 = 7.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 476 8 4 7 2.0 O=C(NCCO)c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
CHEMBL2391812 181610 0 None None None Human 7.9 pIC50 = 7.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 476 8 4 7 2.0 O=C(NCCO)c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
57888919 181970 0 None None None Human 7.9 pIC50 = 7.9 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889974 181970 0 None None None Human 7.9 pIC50 = 7.9 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398727 181970 0 None None None Human 7.9 pIC50 = 7.9 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398729 181970 0 None None None Human 7.9 pIC50 = 7.9 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
21070989 177765 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CCL15/Leukotactin1 from CCR1 in human THP1 cellsDisplacement of [125I]-CCL15/Leukotactin1 from CCR1 in human THP1 cells
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CCL15/Leukotactin1 from CCR1 in human THP1 cellsDisplacement of [125I]-CCL15/Leukotactin1 from CCR1 in human THP1 cells
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
21070983 177766 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 5 0 5 4.3 CCOc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322876 177766 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 5 0 5 4.3 CCOc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
71718022 177776 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 480 5 1 6 3.4 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(CO)c1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322886 177776 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 480 5 1 6 3.4 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(CO)c1Cl 10.1016/j.bmcl.2013.01.005
44430752 178860 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 599 11 2 9 2.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCOCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL234295 178860 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 599 11 2 9 2.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCOCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
11803142 26286 0 None None None Mouse 7.9 pIC50 = 7.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 615 5 1 2 7.8 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
CHEMBL1183314 26286 0 None None None Mouse 7.9 pIC50 = 7.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 615 5 1 2 7.8 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
6918497 232475 1 None None None Mouse 7.9 pIC50 = 7.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
CHEMBL331897 232475 1 None None None Mouse 7.9 pIC50 = 7.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
25175446 258167 0 None None None Human 7.9 pIC50 = 7.9 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 450 3 2 4 4.5 CC(C)(C)OC(=O)N[C@@H]1CCC[C@@H]1C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
CHEMBL3679638 258167 0 None None None Human 7.9 pIC50 = 7.9 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 450 3 2 4 4.5 CC(C)(C)OC(=O)N[C@@H]1CCC[C@@H]1C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
71560163 177739 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 411 5 1 6 2.3 COc1cc(N2CCN(C(=O)Cn3nc(CN)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322850 177739 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 411 5 1 6 2.3 COc1cc(N2CCN(C(=O)Cn3nc(CN)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
57840312 177761 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 382 4 0 5 2.9 COc1cc(N2CCN(C(=O)Cn3ncc(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322871 177761 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 382 4 0 5 2.9 COc1cc(N2CCN(C(=O)Cn3ncc(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
25233754 353229 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 473 4 1 2 5.7 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1Cl 10.1021/jm801416q
CHEMBL473531 353229 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 473 4 1 2 5.7 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1Cl 10.1021/jm801416q
57889591 164290 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 6 1 2 4.6 CCCC(NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180538 164290 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 6 1 2 4.6 CCCC(NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
155549724 347937 0 None None None Human 5.9 pIC50 = 5.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 427 4 1 3 5.4 Cc1c(C(=O)NCc2cccc(C(F)(F)F)c2)cnn1-c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2018.11.015
CHEMBL4539264 347937 0 None None None Human 5.9 pIC50 = 5.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 427 4 1 3 5.4 Cc1c(C(=O)NCc2cccc(C(F)(F)F)c2)cnn1-c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2018.11.015
24758630 164250 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 438 5 1 2 5.4 O=C(N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C1CCCCC1)c1ccccc1 10.1021/jm300896d
CHEMBL2180494 164250 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 438 5 1 2 5.4 O=C(N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C1CCCCC1)c1ccccc1 10.1021/jm300896d
57889696 164281 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 384 5 1 2 4.3 CC[C@@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180527 164281 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 384 5 1 2 4.3 CC[C@@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57888938 182004 0 None None None Human 6.9 pIC50 = 6.9 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 477 6 2 4 3.1 CC(C)[C@@H](NC(=O)c1cccc(S(N)(=O)=O)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2398766 182004 0 None None None Human 6.9 pIC50 = 6.9 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 477 6 2 4 3.1 CC(C)[C@@H](NC(=O)c1cccc(S(N)(=O)=O)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
11124782 237268 0 None None None Human 6.9 pIC50 = 6.9 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 587 11 3 3 7.3 O=C(NCC1CCCCC1)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
CHEMBL341306 237268 0 None None None Human 6.9 pIC50 = 6.9 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 587 11 3 3 7.3 O=C(NCC1CCCCC1)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
44453357 197826 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 434 4 1 4 3.5 O=S(=O)(c1ccccc1)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL270419 197826 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 434 4 1 4 3.5 O=S(=O)(c1ccccc1)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
57889164 182001 0 None None None Human 7.9 pIC50 = 7.9 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 476 5 3 4 4.1 CC(C)[C@@H](NC(=O)c1ccc(F)c(O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398763 182001 0 None None None Human 7.9 pIC50 = 7.9 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 476 5 3 4 4.1 CC(C)[C@@H](NC(=O)c1ccc(F)c(O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
44431529 178851 0 None None None Human 7.9 pIC50 = 7.9 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 490 9 1 5 4.0 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2C(=O)CCC(=O)O)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
CHEMBL234263 178851 0 None None None Human 7.9 pIC50 = 7.9 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 490 9 1 5 4.0 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2C(=O)CCC(=O)O)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
57889660 181981 0 None None None Human 7.9 pIC50 = 7.9 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 380 4 2 3 2.9 CC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL2398740 181981 0 None None None Human 7.9 pIC50 = 7.9 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 380 4 2 3 2.9 CC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
21070989 177765 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CCL15/Leukotactin1 from CCR1 in human monocytesDisplacement of [125I]-CCL15/Leukotactin1 from CCR1 in human monocytes
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CCL15/Leukotactin1 from CCR1 in human monocytesDisplacement of [125I]-CCL15/Leukotactin1 from CCR1 in human monocytes
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
24758296 164213 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 430 6 1 2 4.6 CC(C)[C@@H](NC(=O)Cc1ccccc1F)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180186 164213 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 430 6 1 2 4.6 CC(C)[C@@H](NC(=O)Cc1ccccc1F)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
72945111 214057 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 459 7 3 6 2.8 CNC(=O)Nc1ccc(OC)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2013.11.062
CHEMBL3099960 214057 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 459 7 3 6 2.8 CNC(=O)Nc1ccc(OC)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2013.11.062
68958915 181599 0 None None None Human 6.9 pIC50 = 6.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 470 6 2 6 2.2 O=C(c1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1ccccc1O2)N1CC[C@H](O)C1 10.1016/j.bmcl.2013.04.047
CHEMBL2391801 181599 0 None None None Human 6.9 pIC50 = 6.9 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 470 6 2 6 2.2 O=C(c1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1ccccc1O2)N1CC[C@H](O)C1 10.1016/j.bmcl.2013.04.047
57888652 164291 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 4.9 CC(C)CC(NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180539 164291 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 4.9 CC(C)CC(NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44309267 469006 0 None None None Human 6.9 pIC50 = 6.9 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccc2ccccc2n1 10.1016/j.bmcl.2004.02.021
CHEMBL69978 469006 0 None None None Human 6.9 pIC50 = 6.9 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccc2ccccc2n1 10.1016/j.bmcl.2004.02.021
25231480 373172 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 389 4 1 2 4.1 CN(Cc1ccc(F)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1 10.1021/jm801416q
CHEMBL517261 373172 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 389 4 1 2 4.1 CN(Cc1ccc(F)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1 10.1021/jm801416q
72947880 214053 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 445 5 2 7 3.7 Nc1nc2c(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)cccc2s1 10.1016/j.bmcl.2013.11.062
CHEMBL3099956 214053 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 445 5 2 7 3.7 Nc1nc2c(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)cccc2s1 10.1016/j.bmcl.2013.11.062
69437067 214054 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 444 5 1 6 4.5 Cc1nc2c(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)cccc2s1 10.1016/j.bmcl.2013.11.062
CHEMBL3099957 214054 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 444 5 1 6 4.5 Cc1nc2c(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)cccc2s1 10.1016/j.bmcl.2013.11.062
10628025 25453 0 None None None Mouse 5.9 pIC50 = 5.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 523 6 1 2 7.6 O=C(NC1CC[N+](Cc2ccccc2)(CC2CCCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
CHEMBL1178588 25453 0 None None None Mouse 5.9 pIC50 = 5.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 523 6 1 2 7.6 O=C(NC1CC[N+](Cc2ccccc2)(CC2CCCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
44453464 195673 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 488 4 1 4 3.9 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3cc(F)c(F)c(F)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL256449 195673 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 488 4 1 4 3.9 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3cc(F)c(F)c(F)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
11082578 236898 0 None None None Human 5.9 pIC50 = 5.9 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 603 10 3 3 7.5 O=C(NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1)Nc1cc(F)ccc1F 10.1021/jm0201767
CHEMBL340491 236898 0 None None None Human 5.9 pIC50 = 5.9 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 603 10 3 3 7.5 O=C(NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1)Nc1cc(F)ccc1F 10.1021/jm0201767
71719254 177771 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 528 4 0 5 4.6 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(Br)c1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322881 177771 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 528 4 0 5 4.6 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(Br)c1Cl 10.1016/j.bmcl.2013.01.005
24758297 164264 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 434 5 1 2 4.8 CC(C)[C@@H](NC(=O)c1ccc(F)c(F)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180508 164264 0 None None None Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 434 5 1 2 4.8 CC(C)[C@@H](NC(=O)c1ccc(F)c(F)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
10769447 25459 0 None None None Human 7.9 pIC50 = 7.9 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 447 4 1 2 6.0 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1016/j.ejmech.2020.113085
CHEMBL1178601 25459 0 None None None Human 7.9 pIC50 = 7.9 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 447 4 1 2 6.0 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1016/j.ejmech.2020.113085
10769447 25459 0 None None None Human 7.9 pIC50 = 7.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 447 4 1 2 6.0 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178601 25459 0 None None None Human 7.9 pIC50 = 7.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 447 4 1 2 6.0 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
25175122 258181 0 None None None Human 7.9 pIC50 = 7.9 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 462 4 3 4 3.2 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)[C@@H]2CC[C@H](O)C2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679652 258181 0 None None None Human 7.9 pIC50 = 7.9 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 462 4 3 4 3.2 CC1(C)CN(C(=O)[C@H]2CCC[C@H]2NC(=O)[C@@H]2CC[C@H](O)C2)CC[C@]1(O)c1ccc(Cl)cc1 nan
44537841 1390 22 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MPIF1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MPIF1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MPIF1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MPIF1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MPIF1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MPIF1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MPIF1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MPIF1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MPIF1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MPIF1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
25174956 258179 0 None None None Human 7.8 pIC50 = 7.8 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 465 5 4 4 3.0 C[C@@H](O)CNC(=O)N[C@@H]1CCCC[C@@H]1C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
CHEMBL3679650 258179 0 None None None Human 7.8 pIC50 = 7.8 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 465 5 4 4 3.0 C[C@@H](O)CNC(=O)N[C@@H]1CCCC[C@@H]1C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
24782826 372710 4 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 439 4 1 2 5.0 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1 10.1016/j.bmcl.2010.07.082
CHEMBL514611 372710 4 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 439 4 1 2 5.0 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1 10.1016/j.bmcl.2010.07.082
24782826 372710 4 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 439 4 1 2 5.0 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1 10.1021/jm801416q
CHEMBL514611 372710 4 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 439 4 1 2 5.0 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1 10.1021/jm801416q
57889255 164216 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 6 1 2 4.7 Cc1ccc(CC(=O)N[C@@H](C(=O)N2CCC(c3ccc(Cl)cc3)CC2)C(C)C)cc1 10.1021/jm300896d
CHEMBL2180189 164216 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 6 1 2 4.7 Cc1ccc(CC(=O)N[C@@H](C(=O)N2CCC(c3ccc(Cl)cc3)CC2)C(C)C)cc1 10.1021/jm300896d
44430726 177890 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 502 8 2 7 2.6 CNc1c(Nc2cc(F)c(F)cc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232455 177890 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 502 8 2 7 2.6 CNc1c(Nc2cc(F)c(F)cc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453293 332188 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 486 7 2 4 3.8 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1Br 10.1016/j.bmcl.2007.09.068
CHEMBL429591 332188 0 None None None Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 486 7 2 4 3.8 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1Br 10.1016/j.bmcl.2007.09.068
10765199 222294 0 None None None Human 6.9 pIC50 = 6.9 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 432 4 1 3 5.9 O=C(NC1CCN(CC2CCCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1016/j.ejmech.2020.113085
CHEMBL33074 222294 0 None None None Human 6.9 pIC50 = 6.9 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 432 4 1 3 5.9 O=C(NC1CCN(CC2CCCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1016/j.ejmech.2020.113085
10765199 222294 0 None None None Human 6.9 pIC50 = 6.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 432 4 1 3 5.9 O=C(NC1CCN(CC2CCCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
CHEMBL33074 222294 0 None None None Human 6.9 pIC50 = 6.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 432 4 1 3 5.9 O=C(NC1CCN(CC2CCCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
10676520 25452 0 None None None Mouse 6.9 pIC50 = 6.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 617 5 1 2 7.9 CC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
CHEMBL1178581 25452 0 None None None Mouse 6.9 pIC50 = 6.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 617 5 1 2 7.9 CC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
10509339 26639 0 None None None Mouse 6.9 pIC50 = 6.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 631 6 1 2 8.3 CCC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
CHEMBL1185511 26639 0 None None None Mouse 6.9 pIC50 = 6.9 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 631 6 1 2 8.3 CCC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
44453614 308735 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Br)N1CCC[C@@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
CHEMBL402825 308735 0 None None None Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Br)N1CCC[C@@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
11814253 235826 0 None None None Human 5.9 pIC50 = 5.9 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 635 10 3 3 8.2 O=C(NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1)Nc1cccc(C(F)(F)F)c1 10.1021/jm0201767
CHEMBL338624 235826 0 None None None Human 5.9 pIC50 = 5.9 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 635 10 3 3 8.2 O=C(NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1)Nc1cccc(C(F)(F)F)c1 10.1021/jm0201767
24758044 164277 0 None None None Human 4.8 pIC50 = 4.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57888953 164277 0 None None None Human 4.8 pIC50 = 4.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
71455572 164277 0 None None None Human 4.8 pIC50 = 4.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180523 164277 0 None None None Human 4.8 pIC50 = 4.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180528 164277 0 None None None Human 4.8 pIC50 = 4.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180534 164277 0 None None None Human 4.8 pIC50 = 4.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
21070989 177765 0 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at CCR1 in human monocytes assessed as inhibition of CCL15/Leukotactin1-induced chemotaxisAntagonist activity at CCR1 in human monocytes assessed as inhibition of CCL15/Leukotactin1-induced chemotaxis
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at CCR1 in human monocytes assessed as inhibition of CCL15/Leukotactin1-induced chemotaxisAntagonist activity at CCR1 in human monocytes assessed as inhibition of CCL15/Leukotactin1-induced chemotaxis
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
57889660 181981 0 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 380 4 2 3 2.9 CC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL2398740 181981 0 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 380 4 2 3 2.9 CC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
57889158 181975 0 None None None Human 7.8 pIC50 = 7.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 443 5 2 4 3.6 CC(C)[C@@H](NC(=O)c1ccccn1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398734 181975 0 None None None Human 7.8 pIC50 = 7.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 443 5 2 4 3.6 CC(C)[C@@H](NC(=O)c1ccccn1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
44430754 331491 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 577 10 2 8 3.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2ccccn2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL428193 331491 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 577 10 2 8 3.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2ccccn2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44309165 468964 0 None None None Human 7.8 pIC50 = 7.8 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 490 9 3 6 3.0 CC1CC([C@H](C[C@H](O)[C@H](Cc2ccccc2)NC(=O)c2cnc3ccccc3n2)C(N)=O)CC(C)O1 10.1016/j.bmcl.2004.02.021
CHEMBL69659 468964 0 None None None Human 7.8 pIC50 = 7.8 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 490 9 3 6 3.0 CC1CC([C@H](C[C@H](O)[C@H](Cc2ccccc2)NC(=O)c2cnc3ccccc3n2)C(N)=O)CC(C)O1 10.1016/j.bmcl.2004.02.021
25174462 258176 0 None None None Human 7.8 pIC50 = 7.8 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 496 6 2 3 5.1 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)CCc2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679646 258176 0 None None None Human 7.8 pIC50 = 7.8 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 496 6 2 3 5.1 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)CCc2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
44453202 195665 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 422 7 2 4 3.3 Cc1ccccc1S(=O)(=O)NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL256404 195665 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 422 7 2 4 3.3 Cc1ccccc1S(=O)(=O)NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2007.09.068
10555351 235084 0 None None None Human 6.8 pIC50 = 6.8 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 586 4 1 3 7.3 O=C(NC1CCN(C/C2=C/CCCCCC2)CC1)C1c2cc(Br)ccc2Oc2ccc(Br)cc21 10.1021/jm0004244
CHEMBL33580 235084 0 None None None Human 6.8 pIC50 = 6.8 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 586 4 1 3 7.3 O=C(NC1CCN(C/C2=C/CCCCCC2)CC1)C1c2cc(Br)ccc2Oc2ccc(Br)cc21 10.1021/jm0004244
44309155 461770 0 None None None Human 4.8 pIC50 = 4.8 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@@H](O)[C@@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
CHEMBL69822 461770 0 None None None Human 4.8 pIC50 = 4.8 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@@H](O)[C@@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
24758743 164278 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 364 6 1 2 4.0 CC[C@@H](NC(=O)CC(C)C)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180524 164278 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 364 6 1 2 4.0 CC[C@@H](NC(=O)CC(C)C)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57888775 164293 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 5.0 CCCC(NC(=O)c1ccccc1C)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180541 164293 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 5.0 CCCC(NC(=O)c1ccccc1C)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57889484 182002 0 None None None Human 6.8 pIC50 = 6.8 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 532 7 3 3 5.7 CC(C)[C@@H](NC(=O)c1cccc(-c2ccccc2NC(N)=O)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2398764 182002 0 None None None Human 6.8 pIC50 = 6.8 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 532 7 3 3 5.7 CC(C)[C@@H](NC(=O)c1cccc(-c2ccccc2NC(N)=O)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
11351191 177733 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 440 5 1 6 3.1 COc1cc(N2CCN(C(=O)Cn3nc(C(C)(C)O)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322845 177733 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 440 5 1 6 3.1 COc1cc(N2CCN(C(=O)Cn3nc(C(C)(C)O)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
71718023 177777 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 479 5 1 6 3.3 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(CN)c1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322887 177777 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 479 5 1 6 3.3 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(CN)c1Cl 10.1016/j.bmcl.2013.01.005
44537841 1390 22 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of LKN1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of LKN1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of LKN1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of LKN1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of LKN1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of LKN1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of LKN1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of LKN1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of LKN1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of LKN1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
69437029 214052 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 427 5 1 5 4.6 Cc1cc2c(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)cccc2o1 10.1016/j.bmcl.2013.11.062
CHEMBL3099955 214052 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 427 5 1 5 4.6 Cc1cc2c(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)cccc2o1 10.1016/j.bmcl.2013.11.062
44430742 279220 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 557 11 2 8 2.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN(C)C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL387821 279220 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 557 11 2 8 2.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN(C)C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44430724 298656 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 484 8 2 7 2.5 CNc1c(Nc2cc(F)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL396700 298656 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 484 8 2 7 2.5 CNc1c(Nc2cc(F)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453529 198142 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 414 7 2 5 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccs1 10.1016/j.bmcl.2007.09.068
CHEMBL272097 198142 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 414 7 2 5 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccs1 10.1016/j.bmcl.2007.09.068
44309347 469197 0 None None None Human 6.8 pIC50 = 6.8 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 516 10 3 5 4.4 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccc(Cl)c(Cl)c1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
CHEMBL71242 469197 0 None None None Human 6.8 pIC50 = 6.8 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 516 10 3 5 4.4 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccc(Cl)c(Cl)c1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
10502989 232372 0 None None None Human 5.8 pIC50 = 5.8 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 434 6 2 3 4.9 O=C(NC1CCN(CC2CCCCCCC2)CC1)C(O)(c1ccccc1)c1ccccc1 10.1021/jm0004244
CHEMBL33159 232372 0 None None None Human 5.8 pIC50 = 5.8 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 434 6 2 3 4.9 O=C(NC1CCN(CC2CCCCCCC2)CC1)C(O)(c1ccccc1)c1ccccc1 10.1021/jm0004244
57991685 181964 0 None None None Human 5.8 pIC50 = 5.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@H](N)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398720 181964 0 None None None Human 5.8 pIC50 = 5.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@H](N)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
10875472 232694 0 None None None Human 6.8 pIC50 = 6.8 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 568 10 3 4 6.6 O=C(NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1)Nc1ccncc1 10.1021/jm0201767
CHEMBL332277 232694 0 None None None Human 6.8 pIC50 = 6.8 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 568 10 3 4 6.6 O=C(NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1)Nc1ccncc1 10.1021/jm0201767
44430753 279194 0 None None None Mouse 5.8 pIC50 = 5.8 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 598 11 3 9 2.2 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCNCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL387608 279194 0 None None None Mouse 5.8 pIC50 = 5.8 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 598 11 3 9 2.2 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCNCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44309237 202875 0 None None None Human 4.8 pIC50 = 4.8 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 463 10 4 5 3.4 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cc2ccccc2nc1O 10.1016/j.bmcl.2004.02.021
CHEMBL305420 202875 0 None None None Human 4.8 pIC50 = 4.8 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 463 10 4 5 3.4 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cc2ccccc2nc1O 10.1016/j.bmcl.2004.02.021
71681400 181968 0 None None None Human 7.8 pIC50 = 7.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CCC[C@H]1N)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398725 181968 0 None None None Human 7.8 pIC50 = 7.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CCC[C@H]1N)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
25252974 40088 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 449 4 1 4 5.4 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCC[C@@H]1c1nncn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
CHEMBL1224188 40088 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 449 4 1 4 5.4 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCC[C@@H]1c1nncn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
10580015 25457 0 None None None Human 7.8 pIC50 = 7.8 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 515 4 1 2 7.3 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
CHEMBL1178597 25457 0 None None None Human 7.8 pIC50 = 7.8 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 515 4 1 2 7.3 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
25175450 258171 0 None None None Human 7.8 pIC50 = 7.8 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 482 4 2 4 4.0 CC1(C)CN(C(=O)[C@H]2CC(=O)CC[C@H]2NC(=O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679641 258171 0 None None None Human 7.8 pIC50 = 7.8 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 482 4 2 4 4.0 CC1(C)CN(C(=O)[C@H]2CC(=O)CC[C@H]2NC(=O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
44430735 178812 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 528 10 2 7 3.8 CCCNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL234081 178812 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 528 10 2 7 3.8 CCCNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
57889667 164284 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 458 5 2 3 3.7 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Br)cc2)CC1 10.1021/jm300896d
CHEMBL2180531 164284 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 458 5 2 3 3.7 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Br)cc2)CC1 10.1021/jm300896d
71452035 164268 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 5 1 2 5.1 Cc1cccc(C)c1C(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
CHEMBL2180512 164268 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 5 1 2 5.1 Cc1cccc(C)c1C(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
44430752 178860 0 None None None Mouse 5.8 pIC50 = 5.8 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 599 11 2 9 2.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCOCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL234295 178860 0 None None None Mouse 5.8 pIC50 = 5.8 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 599 11 2 9 2.7 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCOCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
24738063 181996 0 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 419 5 1 3 4.1 CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CCN(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398758 181996 0 None None None Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 419 5 1 3 4.1 CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CCN(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889679 181999 0 None None None Human 7.8 pIC50 = 7.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 442 5 2 3 4.2 CC(C)[C@@H](NC(=O)c1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398761 181999 0 None None None Human 7.8 pIC50 = 7.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 442 5 2 3 4.2 CC(C)[C@@H](NC(=O)c1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57840356 177753 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 436 4 0 5 3.6 COc1cc(N2CCN(C(=O)Cn3cc(Cl)c(C(F)(F)F)n3)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322863 177753 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 436 4 0 5 3.6 COc1cc(N2CCN(C(=O)Cn3cc(Cl)c(C(F)(F)F)n3)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
57889975 164219 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 444 7 1 2 5.0 CC(C)[C@@H](NC(=O)CCc1ccccc1F)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180192 164219 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 444 7 1 2 5.0 CC(C)[C@@H](NC(=O)CCc1ccccc1F)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
24758298 164222 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 455 5 1 4 5.1 CC(C)[C@@H](NC(=O)c1nc2ccccc2s1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180195 164222 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 455 5 1 4 5.1 CC(C)[C@@H](NC(=O)c1nc2ccccc2s1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
71570634 178233 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 411 6 3 6 2.5 CC(=O)Nc1ccc(O)cc1OC[C@@H](N)CN1CCC2(CC1)Cc1ccccc1O2 10.1016/j.bmcl.2012.12.095
CHEMBL2332942 178233 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 411 6 3 6 2.5 CC(=O)Nc1ccc(O)cc1OC[C@@H](N)CN1CCC2(CC1)Cc1ccccc1O2 10.1016/j.bmcl.2012.12.095
44430748 178095 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 529 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232837 178095 0 None None None Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 529 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
25176235 258172 0 None None None Human 7.7 pIC50 = 7.7 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 483 4 3 3 5.2 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)Nc2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679642 258172 0 None None None Human 7.7 pIC50 = 7.7 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 483 4 3 3 5.2 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)Nc2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
25174305 258174 0 None None None Human 7.7 pIC50 = 7.7 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 470 4 2 5 3.6 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)c2cncnc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679644 258174 0 None None None Human 7.7 pIC50 = 7.7 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 470 4 2 5 3.6 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)c2cncnc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
57889141 164275 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 427 6 2 2 4.6 CC(C)[C@@H](NC(=O)NCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180521 164275 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 427 6 2 2 4.6 CC(C)[C@@H](NC(=O)NCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57889796 164299 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 414 5 2 3 3.6 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180548 164299 0 None None None Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 414 5 2 3 3.6 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
73349030 181992 0 None None None Human 5.8 pIC50 = 5.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1ccc(Cl)cc1)C(=O)N1CC[C@@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398751 181992 0 None None None Human 5.8 pIC50 = 5.8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1ccc(Cl)cc1)C(=O)N1CC[C@@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
10555068 26282 0 None None None Human 5.8 pIC50 = 5.8 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 443 4 1 1 6.7 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)c2c3ccccc3cc3ccccc23)CC1 10.1021/jm0004244
CHEMBL1183306 26282 0 None None None Human 5.8 pIC50 = 5.8 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 443 4 1 1 6.7 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)c2c3ccccc3cc3ccccc23)CC1 10.1021/jm0004244
21070982 177781 1 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 3 0 4 4.0 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(Br)cc2)CC1 10.1016/j.bmcl.2013.01.005
CHEMBL2322891 177781 1 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 3 0 4 4.0 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(Br)cc2)CC1 10.1016/j.bmcl.2013.01.005
57889592 164285 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 396 5 1 2 4.4 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CC=C(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180532 164285 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 396 5 1 2 4.4 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CC=C(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44453433 316434 0 None None None Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2007.09.068
CHEMBL411476 316434 0 None None None Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2007.09.068
44309087 202469 0 None None None Human 4.7 pIC50 = 4.7 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccnc2ccccc12 10.1016/j.bmcl.2004.02.021
CHEMBL303947 202469 0 None None None Human 4.7 pIC50 = 4.7 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccnc2ccccc12 10.1016/j.bmcl.2004.02.021
57889180 233479 0 None None None Human 7.7 pIC50 = 7.7 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334726 233479 0 None None None Human 7.7 pIC50 = 7.7 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
57840556 177746 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 416 4 0 5 3.2 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)cc3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322857 177746 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 416 4 0 5 3.2 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)cc3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
24758299 164217 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 440 7 1 2 5.1 Cc1ccccc1CCC(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
CHEMBL2180190 164217 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 440 7 1 2 5.1 Cc1ccccc1CCC(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
795 7884 5 None None None Human 5.7 pIC50 = 5.7 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 480 6 2 6 5.1 O=C(NC1CCN(CC1)Cc1ccc(c(c1)Cl)Cl)CSc1nc2c(s1)cc(cc2)N 10.1016/s0960-894x(01)00176-7
9913085 7884 5 None None None Human 5.7 pIC50 = 5.7 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 480 6 2 6 5.1 O=C(NC1CCN(CC1)Cc1ccc(c(c1)Cl)Cl)CSc1nc2c(s1)cc(cc2)N 10.1016/s0960-894x(01)00176-7
CHEMBL20921 7884 5 None None None Human 5.7 pIC50 = 5.7 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 480 6 2 6 5.1 O=C(NC1CCN(CC1)Cc1ccc(c(c1)Cl)Cl)CSc1nc2c(s1)cc(cc2)N 10.1016/s0960-894x(01)00176-7
44453637 198288 0 None None None Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC[C@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
CHEMBL272758 198288 0 None None None Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC[C@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
10505512 235472 0 None None None Mouse 5.7 pIC50 = 5.7 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 498 4 1 3 7.1 O=C(NC1CCN(C/C2=C/CCCCCC2)CC1)C1c2cc(Cl)ccc2Oc2ccc(Cl)cc21 10.1021/jm0004244
CHEMBL33639 235472 0 None None None Mouse 5.7 pIC50 = 5.7 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 498 4 1 3 7.1 O=C(NC1CCN(C/C2=C/CCCCCC2)CC1)C1c2cc(Cl)ccc2Oc2ccc(Cl)cc21 10.1021/jm0004244
57889625 164296 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 448 6 1 2 5.8 CCCC(NC(=O)c1ccc2ccccc2c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180545 164296 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 448 6 1 2 5.8 CCCC(NC(=O)c1ccc2ccccc2c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57888746 181963 0 None None None Human 6.7 pIC50 = 6.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](N)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889407 181963 0 None None None Human 6.7 pIC50 = 6.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](N)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398719 181963 0 None None None Human 6.7 pIC50 = 6.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](N)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398721 181963 0 None None None Human 6.7 pIC50 = 6.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](N)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
73347500 181994 0 None None None Human 6.7 pIC50 = 6.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 475 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1ccc(Cl)cc1)C(=O)N1CC[C@](N)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398753 181994 0 None None None Human 6.7 pIC50 = 6.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 475 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1ccc(Cl)cc1)C(=O)N1CC[C@](N)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
44453638 327635 0 None None None Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC[C@@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
CHEMBL427834 327635 0 None None None Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC[C@@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
52916803 335526 28 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.1016/j.bmcl.2018.12.024
CHEMBL4456123 335526 28 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.1016/j.bmcl.2018.12.024
57888907 233484 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 437 6 3 3 3.9 CC[C@H](C)NC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1021/jm5003167
CHEMBL3334817 233484 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 437 6 3 3 3.9 CC[C@H](C)NC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1021/jm5003167
11744314 178226 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 446 6 3 6 3.2 CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2012.12.095
CHEMBL2332935 178226 0 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 446 6 3 6 3.2 CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2012.12.095
57840363 177742 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 4 0 5 4.3 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)[C@@H](C)C2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322853 177742 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 4 0 5 4.3 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)[C@@H](C)C2)ccc1Cl 10.1016/j.bmcl.2013.01.005
57889099 233478 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 449 5 3 3 4.1 CC(C)[C@@H](NC(=O)NC1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334725 233478 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 449 5 3 3 4.1 CC(C)[C@@H](NC(=O)NC1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
118714001 233481 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334728 233481 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
57888907 233484 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 437 6 3 3 3.9 CC[C@H](C)NC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1021/jm5003167
CHEMBL3334817 233484 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 437 6 3 3 3.9 CC[C@H](C)NC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1021/jm5003167
118714035 233488 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 439 6 4 4 2.5 CC(C)[C@@H](NC(=O)NC[C@H](C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334821 233488 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 439 6 4 4 2.5 CC(C)[C@@H](NC(=O)NC[C@H](C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
118714036 233489 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 424 6 3 4 2.7 CC(C)[C@@H](NC(=O)C[C@@H](C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334822 233489 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 424 6 3 4 2.7 CC(C)[C@@H](NC(=O)C[C@@H](C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
118714037 233490 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 439 6 4 4 2.5 CC(C)[C@@H](NC(=O)NC[C@@H](C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334823 233490 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 439 6 4 4 2.5 CC(C)[C@@H](NC(=O)NC[C@@H](C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
118714038 233491 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 452 7 3 4 3.5 CC(C)[C@@H](NC(=O)CCC(C)(C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334825 233491 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 452 7 3 4 3.5 CC(C)[C@@H](NC(=O)CCC(C)(C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
10698568 25460 0 None None None Human 8.7 pIC50 = 8.7 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 459 5 1 2 6.3 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1016/j.ejmech.2020.113085
CHEMBL1178613 25460 0 None None None Human 8.7 pIC50 = 8.7 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 459 5 1 2 6.3 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1016/j.ejmech.2020.113085
10698568 25460 0 None None None Human 8.7 pIC50 = 8.7 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 459 5 1 2 6.3 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178613 25460 0 None None None Human 8.7 pIC50 = 8.7 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 459 5 1 2 6.3 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
57889003 181969 9 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889430 181969 9 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398726 181969 9 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398728 181969 9 None None None Human 8.7 pIC50 = 8.7 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
25175283 258166 0 None None None Human 8.7 pIC50 = 8.7 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 468 4 2 3 4.8 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679637 258166 0 None None None Human 8.7 pIC50 = 8.7 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 468 4 2 3 4.8 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
71681399 181967 0 None None None Human 8.7 pIC50 = 8.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CCC[C@@H]1N)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398724 181967 0 None None None Human 8.7 pIC50 = 8.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CCC[C@@H]1N)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889077 181989 0 None None None Human 8.7 pIC50 = 8.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 448 5 2 3 4.5 CC(C)[C@@H](NC(=O)C1CCCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398748 181989 0 None None None Human 8.7 pIC50 = 8.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 448 5 2 3 4.5 CC(C)[C@@H](NC(=O)C1CCCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
59444189 336714 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 510 6 2 7 3.4 CC(C)(CC(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)NC(=O)c1cccc(-n2cnnn2)c1 nan
CHEMBL4473668 336714 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 510 6 2 7 3.4 CC(C)(CC(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)NC(=O)c1cccc(-n2cnnn2)c1 nan
72945511 214043 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 485 8 3 6 3.3 COc1ccc(NC(=O)NC2CC2)c(OC[C@@H](O)CN2CCC3(CC2)Cc2cc(F)ccc2O3)c1 10.1016/j.bmcl.2013.11.062
CHEMBL3099946 214043 0 None None None Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 485 8 3 6 3.3 COc1ccc(NC(=O)NC2CC2)c(OC[C@@H](O)CN2CCC3(CC2)Cc2cc(F)ccc2O3)c1 10.1016/j.bmcl.2013.11.062
57991707 181965 0 None None None Human 8.6 pIC50 = 8.6 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CCC[C@@H]1O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398722 181965 0 None None None Human 8.6 pIC50 = 8.6 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CCC[C@@H]1O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
71680936 181991 0 None None None Human 8.6 pIC50 = 8.6 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 563 8 3 6 3.2 CC(C)[C@@H](NC(=O)C1CCCC1(O)CCN1CCOCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398750 181991 0 None None None Human 8.6 pIC50 = 8.6 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 563 8 3 6 3.2 CC(C)[C@@H](NC(=O)C1CCCC1(O)CCN1CCOCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
52916803 335526 28 None None None Human 8.6 pIC50 = 8.6 Binding
Affinity On-target Cellular interaction (Chemotaxis in THP-1 cells) EUB0000352a CCR1Affinity On-target Cellular interaction (Chemotaxis in THP-1 cells) EUB0000352a CCR1
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL5210121
CHEMBL4456123 335526 28 None None None Human 8.6 pIC50 = 8.6 Binding
Affinity On-target Cellular interaction (Chemotaxis in THP-1 cells) EUB0000352a CCR1Affinity On-target Cellular interaction (Chemotaxis in THP-1 cells) EUB0000352a CCR1
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL5210121
52916803 335526 28 None None None Human 8.6 pIC50 = 8.6 Binding
ChemotaxisChemotaxis
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL4507278
CHEMBL4456123 335526 28 None None None Human 8.6 pIC50 = 8.6 Binding
ChemotaxisChemotaxis
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL4507278
21070989 177765 0 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL23/CKbeta8.1-induced chemotaxisAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL23/CKbeta8.1-induced chemotaxis
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL23/CKbeta8.1-induced chemotaxisAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL23/CKbeta8.1-induced chemotaxis
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
68963393 181598 0 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 504 6 2 6 2.9 O=C(c1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CC[C@H](O)C1 10.1016/j.bmcl.2013.04.047
CHEMBL2391800 181598 0 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 504 6 2 6 2.9 O=C(c1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CC[C@H](O)C1 10.1016/j.bmcl.2013.04.047
10480588 181631 0 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 486 8 2 6 3.5 COc1ccc(C(=O)NC2CC2)c(OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)c1 10.1016/j.bmcl.2013.04.047
CHEMBL2391938 181631 0 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 486 8 2 6 3.5 COc1ccc(C(=O)NC2CC2)c(OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)c1 10.1016/j.bmcl.2013.04.047
57889423 181988 0 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 434 5 2 3 4.1 CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398747 181988 0 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 434 5 2 3 4.1 CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
10555108 25447 0 None None None Human 8.6 pIC50 = 8.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 445 4 1 2 5.9 C[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178543 25447 0 None None None Human 8.6 pIC50 = 8.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 445 4 1 2 5.9 C[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
10094212 178227 0 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 430 6 3 6 2.7 CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2012.12.095
CHEMBL2332936 178227 0 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 430 6 3 6 2.7 CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2012.12.095
57889347 181990 0 None None None Human 8.6 pIC50 = 8.6 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 514 6 2 3 5.5 CC(C)[C@@H](NC(=O)CC12CC3CC(CC(C3)C1)C2)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398749 181990 0 None None None Human 8.6 pIC50 = 8.6 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 514 6 2 3 5.5 CC(C)[C@@H](NC(=O)CC12CC3CC(CC(C3)C1)C2)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889003 181969 9 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at human CCR1 assessed as inhibition of MPIF-1-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MPIF-1-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889430 181969 9 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at human CCR1 assessed as inhibition of MPIF-1-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MPIF-1-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398726 181969 9 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at human CCR1 assessed as inhibition of MPIF-1-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MPIF-1-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398728 181969 9 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at human CCR1 assessed as inhibition of MPIF-1-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MPIF-1-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
10072781 181630 0 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 456 7 2 5 3.4 O=C(NC1CC1)c1ccccc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
CHEMBL2391937 181630 0 None None None Human 8.6 pIC50 = 8.6 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 456 7 2 5 3.4 O=C(NC1CC1)c1ccccc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
10531632 25449 0 None None None Human 8.6 pIC50 = 8.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 473 6 1 2 6.7 CCC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178571 25449 0 None None None Human 8.6 pIC50 = 8.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 473 6 1 2 6.7 CCC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
57888919 181970 0 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889974 181970 0 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398727 181970 0 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398729 181970 0 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889334 181984 0 None None None Human 8.5 pIC50 = 8.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 422 6 2 3 4.0 CC(C)CC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL2398743 181984 0 None None None Human 8.5 pIC50 = 8.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 422 6 2 3 4.0 CC(C)CC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
57889164 182001 0 None None None Human 8.5 pIC50 = 8.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 476 5 3 4 4.1 CC(C)[C@@H](NC(=O)c1ccc(F)c(O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398763 182001 0 None None None Human 8.5 pIC50 = 8.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 476 5 3 4 4.1 CC(C)[C@@H](NC(=O)c1ccc(F)c(O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
71681244 181966 0 None None None Human 7.7 pIC50 = 7.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CCC[C@H]1O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398723 181966 0 None None None Human 7.7 pIC50 = 7.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CCC[C@H]1O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57840282 177734 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 460 4 0 5 3.6 COc1cc(N2CCN(C(=O)Cn3nc(Br)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322846 177734 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 460 4 0 5 3.6 COc1cc(N2CCN(C(=O)Cn3nc(Br)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
25253284 40074 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 450 4 1 5 4.8 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCC[C@@H]1c1nnnn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
CHEMBL1224119 40074 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 450 4 1 5 4.8 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCC[C@@H]1c1nnnn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
24758406 164260 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 404 6 1 2 4.8 CC(C)[C@@H](NC(=O)CC1CCCC1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180504 164260 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 404 6 1 2 4.8 CC(C)[C@@H](NC(=O)CC1CCCC1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57889047 233477 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 457 5 3 3 4.6 CC(C)[C@@H](NC(=O)Nc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334724 233477 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 457 5 3 3 4.6 CC(C)[C@@H](NC(=O)Nc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
44430746 177992 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 530 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCO)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232638 177992 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 530 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCO)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44309195 202240 0 None None None Human 7.7 pIC50 = 7.7 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 496 9 3 5 3.6 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCC(F)(F)CC1 10.1016/j.bmcl.2004.02.022
CHEMBL302533 202240 0 None None None Human 7.7 pIC50 = 7.7 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 496 9 3 5 3.6 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCC(F)(F)CC1 10.1016/j.bmcl.2004.02.022
44430721 291268 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 502 8 2 7 3.1 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(Cl)cc3)CC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL390707 291268 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 502 8 2 7 3.1 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(Cl)cc3)CC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453320 197794 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL270253 197794 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
10525291 236903 0 None None None Human 6.7 pIC50 = 6.7 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 404 4 1 3 5.1 O=C(NC1CCN(CC2CCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1016/j.ejmech.2020.113085
CHEMBL34053 236903 0 None None None Human 6.7 pIC50 = 6.7 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 404 4 1 3 5.1 O=C(NC1CCN(CC2CCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1016/j.ejmech.2020.113085
10525291 236903 0 None None None Human 6.7 pIC50 = 6.7 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 404 4 1 3 5.1 O=C(NC1CCN(CC2CCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
CHEMBL34053 236903 0 None None None Human 6.7 pIC50 = 6.7 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 404 4 1 3 5.1 O=C(NC1CCN(CC2CCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
57991713 181997 0 None None None Human 6.7 pIC50 = 6.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 502 5 2 3 5.4 CC(C)[C@@H](NC(=O)c1ccc(Cl)cc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)C2(CCCC2)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398759 181997 0 None None None Human 6.7 pIC50 = 6.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 502 5 2 3 5.4 CC(C)[C@@H](NC(=O)c1ccc(Cl)cc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)C2(CCCC2)C1 10.1016/j.bmcl.2013.04.079
73350585 181962 0 None None None Human 7.7 pIC50 = 7.7 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 441 5 2 4 3.4 CC(C)[C@@H](NC(=O)c1cccnc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C2(CC2)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398718 181962 0 None None None Human 7.7 pIC50 = 7.7 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 441 5 2 4 3.4 CC(C)[C@@H](NC(=O)c1cccnc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C2(CC2)C1 10.1016/j.bmcl.2013.04.079
71719255 177774 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 507 5 1 6 3.2 CNC(=O)c1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(OC)c1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322884 177774 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 507 5 1 6 3.2 CNC(=O)c1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(OC)c1Cl 10.1016/j.bmcl.2013.01.005
10531239 26675 0 None None None Human 5.7 pIC50 = 5.7 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 449 6 2 2 5.0 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C(O)(c2ccccc2)c2ccccc2)CC1 10.1021/jm0004244
CHEMBL1185795 26675 0 None None None Human 5.7 pIC50 = 5.7 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 449 6 2 2 5.0 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C(O)(c2ccccc2)c2ccccc2)CC1 10.1021/jm0004244
10769447 25459 0 None None None Mouse 5.7 pIC50 = 5.7 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 447 4 1 2 6.0 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178601 25459 0 None None None Mouse 5.7 pIC50 = 5.7 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 447 4 1 2 6.0 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
118714038 233491 0 None None None Human 7.7 pIC50 = 7.7 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 452 7 3 4 3.5 CC(C)[C@@H](NC(=O)CCC(C)(C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334825 233491 0 None None None Human 7.7 pIC50 = 7.7 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 452 7 3 4 3.5 CC(C)[C@@H](NC(=O)CCC(C)(C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
24758408 164218 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 440 7 1 2 5.1 Cc1cccc(CCC(=O)N[C@@H](C(=O)N2CCC(c3ccc(Cl)cc3)CC2)C(C)C)c1 10.1021/jm300896d
CHEMBL2180191 164218 0 None None None Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 440 7 1 2 5.1 Cc1cccc(CCC(=O)N[C@@H](C(=O)N2CCC(c3ccc(Cl)cc3)CC2)C(C)C)c1 10.1021/jm300896d
44309163 202775 0 None None None Human 7.7 pIC50 = 7.7 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 462 11 3 5 3.5 CNC(=O)[C@H](CCC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
CHEMBL304845 202775 0 None None None Human 7.7 pIC50 = 7.7 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 462 11 3 5 3.5 CNC(=O)[C@H](CCC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
71718647 177775 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 521 5 0 6 3.6 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(C(=O)N(C)C)c1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322885 177775 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 521 5 0 6 3.6 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(C(=O)N(C)C)c1Cl 10.1016/j.bmcl.2013.01.005
44430836 178855 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 522 8 2 8 3.5 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(Cl)s3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL234276 178855 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 522 8 2 8 3.5 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(Cl)s3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453162 195643 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 526 4 1 4 4.6 CC1CC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN1S(=O)(=O)c1ccccc1Br 10.1016/j.bmcl.2007.09.068
CHEMBL256272 195643 0 None None None Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 526 4 1 4 4.6 CC1CC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN1S(=O)(=O)c1ccccc1Br 10.1016/j.bmcl.2007.09.068
71682816 181998 0 None None None Human 5.7 pIC50 = 5.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 428 6 2 3 4.7 CC(C)[C@H](CN1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)NC(=O)c1ccccc1 10.1016/j.bmcl.2013.04.079
CHEMBL2398760 181998 0 None None None Human 5.7 pIC50 = 5.7 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 428 6 2 3 4.7 CC(C)[C@H](CN1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)NC(=O)c1ccccc1 10.1016/j.bmcl.2013.04.079
44308819 203236 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.022
44308902 203236 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.022
CHEMBL308243 203236 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.022
CHEMBL68937 203236 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.022
24745662 332413 5 None None None Human 7.6 pIC50 = 7.6 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 484 7 1 5 3.4 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2CS(=O)(=O)O)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
9935062 332413 5 None None None Human 7.6 pIC50 = 7.6 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 484 7 1 5 3.4 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2CS(=O)(=O)O)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
CHEMBL430166 332413 5 None None None Human 7.6 pIC50 = 7.6 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 484 7 1 5 3.4 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2CS(=O)(=O)O)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
57840512 177745 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 4 0 5 4.3 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)C[C@@H]2C)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322856 177745 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 4 0 5 4.3 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)C[C@@H]2C)ccc1Cl 10.1016/j.bmcl.2013.01.005
25233755 353230 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 457 4 1 2 5.2 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1F 10.1021/jm801416q
CHEMBL473532 353230 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 457 4 1 2 5.2 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C(F)(F)F)cc1F 10.1021/jm801416q
44308819 203236 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
44308819 203236 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.021
44308902 203236 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
44308902 203236 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.021
CHEMBL308243 203236 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
CHEMBL308243 203236 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.021
CHEMBL68937 203236 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
CHEMBL68937 203236 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.021
44309124 468838 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 520 11 2 5 4.5 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)N1CCCC1 10.1016/j.bmcl.2004.02.022
CHEMBL68692 468838 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 520 11 2 5 4.5 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)N1CCCC1 10.1016/j.bmcl.2004.02.022
57888663 181972 0 None None None Human 6.6 pIC50 = 6.6 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 521 6 3 5 2.9 CC(C)[C@@H](NC(=O)c1ccc(S(N)(=O)=O)cc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398731 181972 0 None None None Human 6.6 pIC50 = 6.6 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 521 6 3 5 2.9 CC(C)[C@@H](NC(=O)c1ccc(S(N)(=O)=O)cc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
44430718 177637 0 None None None Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 500 8 2 7 3.0 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccccc3F)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232044 177637 0 None None None Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 500 8 2 7 3.0 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccccc3F)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
52916803 335526 28 None None None Human 7.6 pIC50 = 7.6 Binding
Ca fluxCa flux
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL4507278
CHEMBL4456123 335526 28 None None None Human 7.6 pIC50 = 7.6 Binding
Ca fluxCa flux
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL4507278
24758174 164262 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 416 5 1 2 4.6 CC(C)[C@@H](NC(=O)c1cccc(F)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180506 164262 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 416 5 1 2 4.6 CC(C)[C@@H](NC(=O)c1cccc(F)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44453504 195893 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 490 8 2 5 4.7 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1-c1cccs1 10.1016/j.bmcl.2007.09.068
CHEMBL257452 195893 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 490 8 2 5 4.7 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1-c1cccs1 10.1016/j.bmcl.2007.09.068
10505512 235472 0 None None None Human 6.6 pIC50 = 6.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 498 4 1 3 7.1 O=C(NC1CCN(C/C2=C/CCCCCC2)CC1)C1c2cc(Cl)ccc2Oc2ccc(Cl)cc21 10.1021/jm0004244
CHEMBL33639 235472 0 None None None Human 6.6 pIC50 = 6.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 498 4 1 3 7.1 O=C(NC1CCN(C/C2=C/CCCCCC2)CC1)C1c2cc(Cl)ccc2Oc2ccc(Cl)cc21 10.1021/jm0004244
10652533 25451 0 None None None Mouse 6.6 pIC50 = 6.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 603 4 1 2 7.5 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
CHEMBL1178579 25451 0 None None None Mouse 6.6 pIC50 = 6.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 603 4 1 2 7.5 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
10995329 42045 0 None None None Human 6.6 pIC50 = 6.6 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 563 13 4 4 5.5 O=C(NCCCCO)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
CHEMBL126978 42045 0 None None None Human 6.6 pIC50 = 6.6 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 563 13 4 4 5.5 O=C(NCCCCO)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
44308997 468729 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccc2ncccc2c1 10.1016/j.bmcl.2004.02.021
CHEMBL67803 468729 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccc2ncccc2c1 10.1016/j.bmcl.2004.02.021
44537841 1390 22 None None None Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at CCR1 receptor in human whole blood assessed as blocked of MIP-1alpha-mediated CD11b upregulation preincubated for 1 hrAntagonist activity at CCR1 receptor in human whole blood assessed as blocked of MIP-1alpha-mediated CD11b upregulation preincubated for 1 hr
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at CCR1 receptor in human whole blood assessed as blocked of MIP-1alpha-mediated CD11b upregulation preincubated for 1 hrAntagonist activity at CCR1 receptor in human whole blood assessed as blocked of MIP-1alpha-mediated CD11b upregulation preincubated for 1 hr
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at CCR1 receptor in human whole blood assessed as blocked of MIP-1alpha-mediated CD11b upregulation preincubated for 1 hrAntagonist activity at CCR1 receptor in human whole blood assessed as blocked of MIP-1alpha-mediated CD11b upregulation preincubated for 1 hr
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at CCR1 receptor in human whole blood assessed as blocked of MIP-1alpha-mediated CD11b upregulation preincubated for 1 hrAntagonist activity at CCR1 receptor in human whole blood assessed as blocked of MIP-1alpha-mediated CD11b upregulation preincubated for 1 hr
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at CCR1 receptor in human whole blood assessed as blocked of MIP-1alpha-mediated CD11b upregulation preincubated for 1 hrAntagonist activity at CCR1 receptor in human whole blood assessed as blocked of MIP-1alpha-mediated CD11b upregulation preincubated for 1 hr
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
24758176 164266 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 5 1 2 4.8 Cc1ccc(C(=O)N[C@@H](C(=O)N2CCC(c3ccc(Cl)cc3)CC2)C(C)C)cc1 10.1021/jm300896d
CHEMBL2180510 164266 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 5 1 2 4.8 Cc1ccc(C(=O)N[C@@H](C(=O)N2CCC(c3ccc(Cl)cc3)CC2)C(C)C)cc1 10.1021/jm300896d
44430723 177717 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 544 8 2 7 3.1 CNc1c(Nc2cc(Br)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232253 177717 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 544 8 2 7 3.1 CNc1c(Nc2cc(Br)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453200 196032 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.0 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1C(F)(F)F 10.1016/j.bmcl.2007.09.068
CHEMBL258065 196032 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.0 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1C(F)(F)F 10.1016/j.bmcl.2007.09.068
10555351 235084 0 None None None Mouse 5.6 pIC50 = 5.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 586 4 1 3 7.3 O=C(NC1CCN(C/C2=C/CCCCCC2)CC1)C1c2cc(Br)ccc2Oc2ccc(Br)cc21 10.1021/jm0004244
CHEMBL33580 235084 0 None None None Mouse 5.6 pIC50 = 5.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 586 4 1 3 7.3 O=C(NC1CCN(C/C2=C/CCCCCC2)CC1)C1c2cc(Br)ccc2Oc2ccc(Br)cc21 10.1021/jm0004244
73353555 181993 0 None None None Human 4.6 pIC50 = 4.6 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 490 6 1 3 5.5 CO[C@]1(c2ccc(Cl)cc2)CCN(C(=O)[C@H](NC(=O)c2ccc(Cl)cc2)C(C)C)CC1(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL2398752 181993 0 None None None Human 4.6 pIC50 = 4.6 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 490 6 1 3 5.5 CO[C@]1(c2ccc(Cl)cc2)CCN(C(=O)[C@H](NC(=O)c2ccc(Cl)cc2)C(C)C)CC1(C)C 10.1016/j.bmcl.2013.04.079
44309414 213770 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 448 10 3 5 3.1 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnnc2ccccc12 10.1016/j.bmcl.2004.02.021
CHEMBL309338 213770 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 448 10 3 5 3.1 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnnc2ccccc12 10.1016/j.bmcl.2004.02.021
57888812 164292 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 4 1 2 4.9 CC(C)(C)C(NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180540 164292 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 4 1 2 4.9 CC(C)(C)C(NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
24758045 164258 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 392 7 1 2 4.6 CC(C)CCC(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
CHEMBL2180502 164258 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 392 7 1 2 4.6 CC(C)CCC(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
44430713 177592 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 500 8 2 7 3.0 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL231829 177592 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 500 8 2 7 3.0 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44430756 178022 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 577 10 2 8 3.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2ccncc2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232654 178022 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 577 10 2 8 3.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2ccncc2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44309327 468908 0 None None None Human 7.6 pIC50 = 7.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 446 9 3 5 3.0 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCC1 10.1016/j.bmcl.2004.02.021
CHEMBL69274 468908 0 None None None Human 7.6 pIC50 = 7.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 446 9 3 5 3.0 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCC1 10.1016/j.bmcl.2004.02.021
17753030 177887 0 None None None Mouse 6.6 pIC50 = 6.6 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 486 7 2 7 2.5 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(N)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232441 177887 0 None None None Mouse 6.6 pIC50 = 6.6 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 486 7 2 7 2.5 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(N)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
10873705 199544 9 None None None Human 6.6 pIC50 = 6.6 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 431 6 1 5 4.8 O=C(CSc1nc2ccccc2s1)NC1CCN(Cc2ccc(Cl)cc2)CC1 10.1016/s0960-894x(01)00176-7
CHEMBL282285 199544 9 None None None Human 6.6 pIC50 = 6.6 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 431 6 1 5 4.8 O=C(CSc1nc2ccccc2s1)NC1CCN(Cc2ccc(Cl)cc2)CC1 10.1016/s0960-894x(01)00176-7
44309178 203142 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 466 10 3 5 3.3 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccc(F)cc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
CHEMBL307535 203142 0 None None None Human 5.6 pIC50 = 5.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 466 10 3 5 3.3 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccc(F)cc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
57390926 140135 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]-MIP-1alpha 125I]-MCP1 from CCR1 expressed in CHO-K1 cells by scintillation proximity assayDisplacement of [125I]-MIP-1alpha 125I]-MCP1 from CCR1 expressed in CHO-K1 cells by scintillation proximity assay
ChEMBL 427 7 2 6 2.6 Cc1noc(C)c1S(=O)(=O)NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2011.09.013
CHEMBL1910159 140135 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]-MIP-1alpha 125I]-MCP1 from CCR1 expressed in CHO-K1 cells by scintillation proximity assayDisplacement of [125I]-MIP-1alpha 125I]-MCP1 from CCR1 expressed in CHO-K1 cells by scintillation proximity assay
ChEMBL 427 7 2 6 2.6 Cc1noc(C)c1S(=O)(=O)NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2011.09.013
57888925 164295 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 4 1 2 5.2 Cc1ccccc1C(=O)NC(C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)(C)C 10.1021/jm300896d
CHEMBL2180544 164295 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 4 1 2 5.2 Cc1ccccc1C(=O)NC(C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)(C)C 10.1021/jm300896d
57889874 164271 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 414 5 1 3 4.9 CC(C)C(NC(=O)Oc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180517 164271 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 414 5 1 3 4.9 CC(C)C(NC(=O)Oc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44309122 202876 0 None None None Human 7.6 pIC50 = 7.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 482 11 4 6 3.4 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)NO 10.1016/j.bmcl.2004.02.022
CHEMBL305423 202876 0 None None None Human 7.6 pIC50 = 7.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 482 11 4 6 3.4 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)NO 10.1016/j.bmcl.2004.02.022
25231300 348333 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 419 5 1 2 5.0 CCN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1 10.1021/jm801416q
CHEMBL454942 348333 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 419 5 1 2 5.0 CCN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1 10.1021/jm801416q
25231301 348417 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 405 4 1 2 4.6 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1 10.1021/jm801416q
CHEMBL455162 348417 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 405 4 1 2 4.6 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1 10.1021/jm801416q
44430716 177635 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 560 8 2 7 3.6 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(Br)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232042 177635 0 None None None Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 560 8 2 7 3.6 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(Br)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
10531632 25449 0 None None None Mouse 6.6 pIC50 = 6.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 473 6 1 2 6.7 CCC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178571 25449 0 None None None Mouse 6.6 pIC50 = 6.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 473 6 1 2 6.7 CCC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
10507823 25455 0 None None None Mouse 6.6 pIC50 = 6.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 475 6 1 2 6.8 CCC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178590 25455 0 None None None Mouse 6.6 pIC50 = 6.6 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 475 6 1 2 6.8 CCC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
21071083 177762 0 None None None Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 416 4 0 5 3.2 COc1cccc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)c1 10.1016/j.bmcl.2013.01.005
CHEMBL2322872 177762 0 None None None Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 416 4 0 5 3.2 COc1cccc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)c1 10.1016/j.bmcl.2013.01.005
59278314 334482 29 None None None Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 425 5 1 7 2.3 CS(=O)(=O)c1cc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)ccn1 10.1016/j.bmcl.2018.12.024
CHEMBL4441094 334482 29 None None None Human 7.6 pIC50 = 7.6 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 425 5 1 7 2.3 CS(=O)(=O)c1cc(CNC(=O)c2cncc3c2cnn3-c2ccc(F)cc2)ccn1 10.1016/j.bmcl.2018.12.024
24758044 164277 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57888953 164277 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
71455572 164277 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180523 164277 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180528 164277 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180534 164277 0 None None None Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
10049340 202703 0 None None None Human 7.6 pIC50 = 7.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 448 11 3 5 3.3 CC(C)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.021
10049340 202703 0 None None None Human 7.6 pIC50 = 7.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 448 11 3 5 3.3 CC(C)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
CHEMBL304358 202703 0 None None None Human 7.6 pIC50 = 7.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 448 11 3 5 3.3 CC(C)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.021
CHEMBL304358 202703 0 None None None Human 7.6 pIC50 = 7.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 448 11 3 5 3.3 CC(C)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
44309105 468819 0 None None None Human 6.6 pIC50 = 6.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 468 10 3 5 3.1 NC(=O)[C@H](Cc1ccccc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
CHEMBL68551 468819 0 None None None Human 6.6 pIC50 = 6.6 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 468 10 3 5 3.1 NC(=O)[C@H](Cc1ccccc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
71460999 164297 0 None None None Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 416 5 3 4 2.3 CC(O)C(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180546 164297 0 None None None Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 416 5 3 4 2.3 CC(O)C(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
73355055 181995 0 None None None Human 7.5 pIC50 = 7.5 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 427 5 1 3 4.5 CC(C)[C@@H](NC(=O)c1cccnc1)C(=O)N1CC[C@H](c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398757 181995 0 None None None Human 7.5 pIC50 = 7.5 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 427 5 1 3 4.5 CC(C)[C@@H](NC(=O)c1cccnc1)C(=O)N1CC[C@H](c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
25233582 373199 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 401 5 1 3 4.0 COc1ccc(NC(=O)N2CCC[C@@H]2C(=O)N(C)Cc2ccc(Cl)cc2)cc1 10.1021/jm801416q
CHEMBL517290 373199 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 401 5 1 3 4.0 COc1ccc(NC(=O)N2CCC[C@@H]2C(=O)N(C)Cc2ccc(Cl)cc2)cc1 10.1021/jm801416q
44309213 468719 0 None None None Human 5.5 pIC50 = 5.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 478 11 3 6 3.1 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccc(OC)cc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
CHEMBL67757 468719 0 None None None Human 5.5 pIC50 = 5.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 478 11 3 6 3.1 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccc(OC)cc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
44430720 177714 0 None None None Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 500 8 2 7 3.0 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3cccc(F)c3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232251 177714 0 None None None Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 500 8 2 7 3.0 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3cccc(F)c3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
57888758 181973 0 None None None Human 5.5 pIC50 = 5.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 486 6 3 4 3.9 CC(C)[C@@H](NC(=O)c1ccccc1C(=O)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398732 181973 0 None None None Human 5.5 pIC50 = 5.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 486 6 3 4 3.9 CC(C)[C@@H](NC(=O)c1ccccc1C(=O)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
11828215 233470 0 None None None Human 6.5 pIC50 = 6.5 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 613 12 3 3 7.1 O=C(NCCc1ccc(F)cc1)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
CHEMBL333422 233470 0 None None None Human 6.5 pIC50 = 6.5 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 613 12 3 3 7.1 O=C(NCCc1ccc(F)cc1)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
25233753 350934 0 None None None Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 439 4 1 2 5.0 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1cccc(C(F)(F)F)c1 10.1021/jm801416q
CHEMBL462442 350934 0 None None None Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 439 4 1 2 5.0 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1cccc(C(F)(F)F)c1 10.1021/jm801416q
57889099 233478 0 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 449 5 3 3 4.1 CC(C)[C@@H](NC(=O)NC1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334725 233478 0 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 449 5 3 3 4.1 CC(C)[C@@H](NC(=O)NC1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
57889314 181986 0 None None None Human 8.5 pIC50 = 8.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 406 5 2 3 3.3 CC(C)[C@@H](NC(=O)C1CC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398745 181986 0 None None None Human 8.5 pIC50 = 8.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 406 5 2 3 3.3 CC(C)[C@@H](NC(=O)C1CC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57888900 182005 0 None None None Human 8.5 pIC50 = 8.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 521 6 3 5 2.9 CC(C)[C@@H](NC(=O)c1cccc(S(N)(=O)=O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398767 182005 0 None None None Human 8.5 pIC50 = 8.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 521 6 3 5 2.9 CC(C)[C@@H](NC(=O)c1cccc(S(N)(=O)=O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
44537841 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889736 233480 0 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334727 233480 0 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
57888785 233482 0 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334815 233482 0 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
57889188 233483 0 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 437 6 3 3 3.9 CC[C@@H](C)NC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1021/jm5003167
CHEMBL3334816 233483 0 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 437 6 3 3 3.9 CC[C@@H](C)NC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1021/jm5003167
57991707 181965 0 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CCC[C@@H]1O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398722 181965 0 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CCC[C@@H]1O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
10509339 26639 0 None None None Human 8.5 pIC50 = 8.5 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 631 6 1 2 8.3 CCC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
CHEMBL1185511 26639 0 None None None Human 8.5 pIC50 = 8.5 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 631 6 1 2 8.3 CCC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
10094211 181592 0 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 430 6 3 6 2.1 CNC(=O)c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2013.04.047
CHEMBL2391794 181592 0 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 430 6 3 6 2.1 CNC(=O)c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2013.04.047
44537841 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC4-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC4-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC4-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC4-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC4-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC4-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC4-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC4-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC4-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC4-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
10393066 214045 0 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 447 6 4 6 2.7 NC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.11.062
CHEMBL3099948 214045 0 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 447 6 4 6 2.7 NC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.11.062
72945112 214058 0 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 445 6 4 6 2.5 CNC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2013.11.062
CHEMBL3099961 214058 0 None None None Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 445 6 4 6 2.5 CNC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2013.11.062
44537841 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of RANTES-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of RANTES-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of RANTES-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of RANTES-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of RANTES-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of RANTES-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of RANTES-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of RANTES-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of RANTES-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of RANTES-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57888895 181971 0 None None None Human 8.5 pIC50 = 8.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1ccc(Cl)cc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398730 181971 0 None None None Human 8.5 pIC50 = 8.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1ccc(Cl)cc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
10676520 25452 0 None None None Human 8.5 pIC50 = 8.5 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 617 5 1 2 7.9 CC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
CHEMBL1178581 25452 0 None None None Human 8.5 pIC50 = 8.5 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 617 5 1 2 7.9 CC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
57889023 182003 0 None None None Human 8.5 pIC50 = 8.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 576 7 4 4 5.4 CC(C)[C@@H](NC(=O)c1cccc(-c2ccccc2NC(N)=O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398765 182003 0 None None None Human 8.5 pIC50 = 8.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 576 7 4 4 5.4 CC(C)[C@@H](NC(=O)c1cccc(-c2ccccc2NC(N)=O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889764 182007 0 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 457 6 2 4 3.6 CC(C)[C@@H](NC(=O)Cc1ccncc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398769 182007 0 None None None Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 457 6 2 4 3.6 CC(C)[C@@H](NC(=O)Cc1ccncc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889843 181982 0 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 394 5 2 3 3.3 CCC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL2398741 181982 0 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 394 5 2 3 3.3 CCC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
10507823 25455 0 None None None Human 8.4 pIC50 = 8.4 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 475 6 1 2 6.8 CCC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178590 25455 0 None None None Human 8.4 pIC50 = 8.4 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 475 6 1 2 6.8 CCC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
73355055 181995 0 None None None Human 8.4 pIC50 = 8.4 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 427 5 1 3 4.5 CC(C)[C@@H](NC(=O)c1cccnc1)C(=O)N1CC[C@H](c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398757 181995 0 None None None Human 8.4 pIC50 = 8.4 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 427 5 1 3 4.5 CC(C)[C@@H](NC(=O)c1cccnc1)C(=O)N1CC[C@H](c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
21070989 177765 0 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced chemotaxisAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced chemotaxis
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced chemotaxisAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced chemotaxis
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
10652533 25451 0 None None None Human 8.4 pIC50 = 8.4 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 603 4 1 2 7.5 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
CHEMBL1178579 25451 0 None None None Human 8.4 pIC50 = 8.4 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 603 4 1 2 7.5 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Br)ccc3Oc3ccc(Br)cc32)CC1 10.1021/jm0004244
44431524 292015 0 None None None Human 7.5 pIC50 = 7.5 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 476 8 2 5 2.7 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2C(=O)NCCN)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
CHEMBL391302 292015 0 None None None Human 7.5 pIC50 = 7.5 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 476 8 2 5 2.7 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2C(=O)NCCN)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
24758044 164277 0 None None None Human 7.5 pIC50 = 7.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
57888953 164277 0 None None None Human 7.5 pIC50 = 7.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
71455572 164277 0 None None None Human 7.5 pIC50 = 7.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2180523 164277 0 None None None Human 7.5 pIC50 = 7.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2180528 164277 0 None None None Human 7.5 pIC50 = 7.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2180534 164277 0 None None None Human 7.5 pIC50 = 7.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
24758294 164252 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 4.4 CC(C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
24758856 164252 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 4.4 CC(C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180496 164252 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 4.4 CC(C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180514 164252 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 4.4 CC(C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44453359 197863 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 408 7 2 4 3.0 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1016/j.bmcl.2007.09.068
CHEMBL270631 197863 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 408 7 2 4 3.0 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1016/j.bmcl.2007.09.068
21070989 177765 0 None None None Mouse 5.5 pIC50 = 5.5 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in mouse WEHI274.1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in mouse WEHI274.1 cells
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None None None Mouse 5.5 pIC50 = 5.5 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in mouse WEHI274.1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in mouse WEHI274.1 cells
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
44308819 203236 0 None None None Human 4.5 pIC50 = 4.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
44308902 203236 0 None None None Human 4.5 pIC50 = 4.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
CHEMBL308243 203236 0 None None None Human 4.5 pIC50 = 4.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
CHEMBL68937 203236 0 None None None Human 4.5 pIC50 = 4.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 453 10 3 4 4.5 CNC(=O)[C@@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
57888688 164273 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 448 7 1 3 4.2 CC(C)C(NS(=O)(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180519 164273 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 448 7 1 3 4.2 CC(C)C(NS(=O)(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
1370410 177778 10 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 404 3 0 4 3.4 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(F)cc2)CC1 10.1016/j.bmcl.2013.01.005
CHEMBL2322888 177778 10 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 404 3 0 4 3.4 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(F)cc2)CC1 10.1016/j.bmcl.2013.01.005
512282 1562 44 None None None Human 7.5 pIC50 = 7.5 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2007.03.037
767 1562 44 None None None Human 7.5 pIC50 = 7.5 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2007.03.037
CHEMBL232656 1562 44 None None None Human 7.5 pIC50 = 7.5 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2007.03.037
10995218 40500 0 None None None Human 7.5 pIC50 = 7.5 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 549 12 4 4 5.1 O=C(NCCCO)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
CHEMBL124127 40500 0 None None None Human 7.5 pIC50 = 7.5 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 549 12 4 4 5.1 O=C(NCCCO)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
10974378 233316 0 None None None Human 6.5 pIC50 = 6.5 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 664 12 3 4 7.4 O=C(NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1)NC1CCN(Cc2ccccc2)CC1 10.1021/jm0201767
CHEMBL333063 233316 0 None None None Human 6.5 pIC50 = 6.5 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 664 12 3 4 7.4 O=C(NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1)NC1CCN(Cc2ccccc2)CC1 10.1021/jm0201767
10255511 181609 0 None None None Human 7.5 pIC50 = 7.5 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 502 6 2 7 2.7 O=C(c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CCOCC1 10.1016/j.bmcl.2013.04.047
CHEMBL2391811 181609 0 None None None Human 7.5 pIC50 = 7.5 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 502 6 2 7 2.7 O=C(c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CCOCC1 10.1016/j.bmcl.2013.04.047
25254218 40075 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 449 4 1 4 5.4 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCC[C@@H]1c1ncnn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
CHEMBL1224120 40075 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 449 4 1 4 5.4 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCC[C@@H]1c1ncnn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
24758172 164265 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 5 1 2 4.8 Cc1ccccc1C(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
24759191 164265 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 5 1 2 4.8 Cc1ccccc1C(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
CHEMBL2180509 164265 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 5 1 2 4.8 Cc1ccccc1C(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
CHEMBL2180542 164265 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 5 1 2 4.8 Cc1ccccc1C(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
24758173 164279 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 378 6 1 2 4.2 CC(C)CC(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
CHEMBL2180525 164279 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 378 6 1 2 4.2 CC(C)CC(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
11464915 214049 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 442 5 2 5 3.4 O=C1CCc2cccc(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)c2N1 10.1016/j.bmcl.2013.11.062
CHEMBL3099952 214049 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 442 5 2 5 3.4 O=C1CCc2cccc(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)c2N1 10.1016/j.bmcl.2013.11.062
68817337 178230 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 425 7 2 6 2.8 COc1ccc(NC(C)=O)c(OC[C@@H](N)CN2CCC3(CC2)Cc2ccccc2O3)c1 10.1016/j.bmcl.2012.12.095
CHEMBL2332939 178230 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 425 7 2 6 2.8 COc1ccc(NC(C)=O)c(OC[C@@H](N)CN2CCC3(CC2)Cc2ccccc2O3)c1 10.1016/j.bmcl.2012.12.095
44453161 195642 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 482 4 1 4 4.5 CC1CC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN1S(=O)(=O)c1ccccc1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL256271 195642 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 482 4 1 4 4.5 CC1CC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN1S(=O)(=O)c1ccccc1Cl 10.1016/j.bmcl.2007.09.068
21071096 177783 0 None None None Human 4.5 pIC50 = 4.5 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 416 4 0 5 3.2 COc1ccc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc1 10.1016/j.bmcl.2013.01.005
CHEMBL2322893 177783 0 None None None Human 4.5 pIC50 = 4.5 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 416 4 0 5 3.2 COc1ccc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc1 10.1016/j.bmcl.2013.01.005
57889972 164301 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 428 6 2 3 4.0 CC(C)CC(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180550 164301 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 428 6 2 3 4.0 CC(C)CC(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
21071106 177828 1 None None None Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 400 3 0 4 3.5 Cc1cccc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)c1 10.1016/j.bmcl.2013.01.005
CHEMBL2323422 177828 1 None None None Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 400 3 0 4 3.5 Cc1cccc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)c1 10.1016/j.bmcl.2013.01.005
71457362 164280 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 392 7 1 2 4.6 CC[C@@H](C)[C@@H](NC(=O)CC(C)C)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180526 164280 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 392 7 1 2 4.6 CC[C@@H](C)[C@@H](NC(=O)CC(C)C)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
21071046 177736 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 397 4 1 6 2.4 COc1cc(N2CCN(C(=O)Cn3nc(N)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322848 177736 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 397 4 1 6 2.4 COc1cc(N2CCN(C(=O)Cn3nc(N)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
21070990 177756 0 None None None Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 512 5 0 5 5.2 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3ccccc3)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322866 177756 0 None None None Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 512 5 0 5 5.2 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3ccccc3)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
57888746 181963 0 None None None Human 6.5 pIC50 = 6.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](N)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889407 181963 0 None None None Human 6.5 pIC50 = 6.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](N)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398719 181963 0 None None None Human 6.5 pIC50 = 6.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](N)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398721 181963 0 None None None Human 6.5 pIC50 = 6.5 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](N)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
44309161 468792 0 None None None Human 5.5 pIC50 = 5.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 462 9 3 6 2.3 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCOCC1 10.1016/j.bmcl.2004.02.022
44309166 468792 0 None None None Human 5.5 pIC50 = 5.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 462 9 3 6 2.3 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCOCC1 10.1016/j.bmcl.2004.02.022
CHEMBL68368 468792 0 None None None Human 5.5 pIC50 = 5.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 462 9 3 6 2.3 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCOCC1 10.1016/j.bmcl.2004.02.022
CHEMBL69876 468792 0 None None None Human 5.5 pIC50 = 5.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 462 9 3 6 2.3 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCOCC1 10.1016/j.bmcl.2004.02.022
24758171 164255 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 7 1 2 4.8 CC(C)[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
24759081 164255 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 7 1 2 4.8 CC(C)[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180499 164255 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 7 1 2 4.8 CC(C)[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180515 164255 0 None None None Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 7 1 2 4.8 CC(C)[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44430714 177593 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 482 8 2 7 2.8 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccccc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL231830 177593 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 482 8 2 7 2.8 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccccc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453503 195455 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 490 8 2 5 4.7 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1-c1ccsc1 10.1016/j.bmcl.2007.09.068
CHEMBL255338 195455 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 490 8 2 5 4.7 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1-c1ccsc1 10.1016/j.bmcl.2007.09.068
44453164 196096 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 492 8 2 5 3.9 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1OC(F)(F)F 10.1016/j.bmcl.2007.09.068
CHEMBL258361 196096 0 None None None Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 492 8 2 5 3.9 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1OC(F)(F)F 10.1016/j.bmcl.2007.09.068
10555108 25447 0 None None None Mouse 6.5 pIC50 = 6.5 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 445 4 1 2 5.9 C[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178543 25447 0 None None None Mouse 6.5 pIC50 = 6.5 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 445 4 1 2 5.9 C[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
44309161 468792 0 None None None Human 5.5 pIC50 = 5.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 462 9 3 6 2.3 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCOCC1 10.1016/j.bmcl.2004.02.021
44309166 468792 0 None None None Human 5.5 pIC50 = 5.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 462 9 3 6 2.3 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCOCC1 10.1016/j.bmcl.2004.02.021
CHEMBL68368 468792 0 None None None Human 5.5 pIC50 = 5.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 462 9 3 6 2.3 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCOCC1 10.1016/j.bmcl.2004.02.021
CHEMBL69876 468792 0 None None None Human 5.5 pIC50 = 5.5 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 462 9 3 6 2.3 NC(=O)[C@@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCOCC1 10.1016/j.bmcl.2004.02.021
44453195 311166 0 None None None Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 496 4 1 4 4.8 Cc1cccc(Cl)c1S(=O)(=O)N1CCC(C)(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL402327 311166 0 None None None Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 496 4 1 4 4.8 Cc1cccc(Cl)c1S(=O)(=O)N1CCC(C)(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
24758172 164265 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 5 1 2 4.8 Cc1ccccc1C(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
24759191 164265 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 5 1 2 4.8 Cc1ccccc1C(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
CHEMBL2180509 164265 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 5 1 2 4.8 Cc1ccccc1C(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
CHEMBL2180542 164265 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 5 1 2 4.8 Cc1ccccc1C(=O)N[C@@H](C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
44453400 195899 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 460 7 2 4 3.8 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(F)cc1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL257509 195899 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 460 7 2 4 3.8 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(F)cc1Cl 10.1016/j.bmcl.2007.09.068
11104005 236207 0 None None None Human 6.4 pIC50 = 6.4 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 602 12 3 4 6.2 O=C(NCCN1CCCCC1)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
CHEMBL339752 236207 0 None None None Human 6.4 pIC50 = 6.4 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 602 12 3 4 6.2 O=C(NCCN1CCCCC1)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
11113940 161061 0 None None None Human 5.4 pIC50 = 5.4 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 509 8 1 6 5.9 CCOc1ccc2nc(SCC(=O)NC3CCN(Cc4ccc(Cl)c(Cl)c4)CC3)sc2c1 10.1016/s0960-894x(01)00176-7
CHEMBL21143 161061 0 None None None Human 5.4 pIC50 = 5.4 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 509 8 1 6 5.9 CCOc1ccc2nc(SCC(=O)NC3CCN(Cc4ccc(Cl)c(Cl)c4)CC3)sc2c1 10.1016/s0960-894x(01)00176-7
25231299 372207 0 None None None Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 433 6 1 2 5.4 CCCN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1 10.1021/jm801416q
CHEMBL509457 372207 0 None None None Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 433 6 1 2 5.4 CCCN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1 10.1021/jm801416q
44453226 196101 0 None None None Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 536 4 1 4 5.4 O=S(=O)(c1ccc(Cl)c(Cl)c1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL258369 196101 0 None None None Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 536 4 1 4 5.4 O=S(=O)(c1ccc(Cl)c(Cl)c1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
21071108 177782 0 None None None Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 400 3 0 4 3.5 Cc1ccc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc1 10.1016/j.bmcl.2013.01.005
CHEMBL2322892 177782 0 None None None Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 400 3 0 4 3.5 Cc1ccc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc1 10.1016/j.bmcl.2013.01.005
57840518 177741 1 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 4 0 5 4.3 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)[C@H](C)C2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322852 177741 1 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 4 0 5 4.3 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)[C@H](C)C2)ccc1Cl 10.1016/j.bmcl.2013.01.005
69439557 214050 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 440 5 2 5 3.4 O=c1ccc2cccc(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)c2[nH]1 10.1016/j.bmcl.2013.11.062
CHEMBL3099953 214050 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 440 5 2 5 3.4 O=c1ccc2cccc(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)c2[nH]1 10.1016/j.bmcl.2013.11.062
57888963 164298 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 4 2 3 3.5 C/C=C(/NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180547 164298 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 4 2 3 3.5 C/C=C(/NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44453290 197728 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 482 4 1 4 4.4 Cc1cccc(Cl)c1S(=O)(=O)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL269956 197728 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 482 4 1 4 4.4 Cc1cccc(Cl)c1S(=O)(=O)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
10628025 25453 0 None None None Human 6.4 pIC50 = 6.4 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 523 6 1 2 7.6 O=C(NC1CC[N+](Cc2ccccc2)(CC2CCCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
CHEMBL1178588 25453 0 None None None Human 6.4 pIC50 = 6.4 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 523 6 1 2 7.6 O=C(NC1CC[N+](Cc2ccccc2)(CC2CCCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
24740170 164288 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 433 5 1 3 4.1 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CCN(c2ccc(Cl)c(Cl)c2)CC1 10.1021/jm300896d
CHEMBL2180536 164288 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 433 5 1 3 4.1 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CCN(c2ccc(Cl)c(Cl)c2)CC1 10.1021/jm300896d
44431527 178850 0 None None None Human 7.4 pIC50 = 7.4 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 448 7 1 4 3.6 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2CC(=O)O)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
CHEMBL234262 178850 0 None None None Human 7.4 pIC50 = 7.4 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 448 7 1 4 3.6 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2CC(=O)O)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
71457361 164253 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 7 1 2 4.8 CC[C@@H](C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180497 164253 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 7 1 2 4.8 CC[C@@H](C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44453265 195757 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 442 7 2 4 3.6 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(Cl)c1 10.1016/j.bmcl.2007.09.068
CHEMBL256821 195757 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 442 7 2 4 3.6 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(Cl)c1 10.1016/j.bmcl.2007.09.068
10579693 25448 0 None None None Mouse 6.4 pIC50 = 6.4 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 489 7 1 2 7.2 CCCC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178558 25448 0 None None None Mouse 6.4 pIC50 = 6.4 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 489 7 1 2 7.2 CCCC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
57396208 140136 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-MIP-1alpha 125I]-MCP1 from CCR1 expressed in CHO-K1 cells by scintillation proximity assayDisplacement of [125I]-MIP-1alpha 125I]-MCP1 from CCR1 expressed in CHO-K1 cells by scintillation proximity assay
ChEMBL 463 9 2 3 4.3 O=C(NCCCCN1CCC(Oc2ccc(F)cc2)C1)NCc1ccc(Br)cc1 10.1016/j.bmcl.2011.09.013
CHEMBL1910160 140136 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-MIP-1alpha 125I]-MCP1 from CCR1 expressed in CHO-K1 cells by scintillation proximity assayDisplacement of [125I]-MIP-1alpha 125I]-MCP1 from CCR1 expressed in CHO-K1 cells by scintillation proximity assay
ChEMBL 463 9 2 3 4.3 O=C(NCCCCN1CCC(Oc2ccc(F)cc2)C1)NCc1ccc(Br)cc1 10.1016/j.bmcl.2011.09.013
24759740 164289 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 364 5 1 2 3.8 CC(C)C(=O)NC(C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
CHEMBL2180537 164289 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 364 5 1 2 3.8 CC(C)C(=O)NC(C(=O)N1CCC(c2ccc(Cl)cc2)CC1)C(C)C 10.1021/jm300896d
44453641 198235 0 None None None Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 438 8 2 5 3.0 COc1ccc(S(=O)(=O)NCCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL272559 198235 0 None None None Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 438 8 2 5 3.0 COc1ccc(S(=O)(=O)NCCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1 10.1016/j.bmcl.2007.09.068
3497 2447 26 None None None Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2018.11.015
44309353 2447 26 None None None Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2018.11.015
5311123 2447 26 None None None Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2018.11.015
CHEMBL1628706 2447 26 None None None Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2018.11.015
CHEMBL308473 2447 26 None None None Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2018.11.015
44453157 311251 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 482 4 1 4 4.4 Cc1cccc(Cl)c1S(=O)(=O)N1CCC[C@@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
CHEMBL402827 311251 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 482 4 1 4 4.4 Cc1cccc(Cl)c1S(=O)(=O)N1CCC[C@@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
10164 1805 30 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 451 4 1 8 2.2 COc1cc(ccc1Cl)N1CCN(CC1)C(=O)Cn1[nH]c(=C2N=CC=N2)c2c1nccc2 10.1016/j.bmcl.2018.11.015
135565361 1805 30 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 451 4 1 8 2.2 COc1cc(ccc1Cl)N1CCN(CC1)C(=O)Cn1[nH]c(=C2N=CC=N2)c2c1nccc2 10.1016/j.bmcl.2018.11.015
25016615 1805 30 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 451 4 1 8 2.2 COc1cc(ccc1Cl)N1CCN(CC1)C(=O)Cn1[nH]c(=C2N=CC=N2)c2c1nccc2 10.1016/j.bmcl.2018.11.015
CHEMBL4444976 1805 30 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 451 4 1 8 2.2 COc1cc(ccc1Cl)N1CCN(CC1)C(=O)Cn1[nH]c(=C2N=CC=N2)c2c1nccc2 10.1016/j.bmcl.2018.11.015
DB12963 1805 30 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of chemotaxis after 30 mins by Celltiter-glo reagent based luminescence assay
ChEMBL 451 4 1 8 2.2 COc1cc(ccc1Cl)N1CCN(CC1)C(=O)Cn1[nH]c(=C2N=CC=N2)c2c1nccc2 10.1016/j.bmcl.2018.11.015
118714001 233481 0 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334728 233481 0 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
57889003 181969 9 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at human CCR1 assessed as inhibition of HCC-1-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of HCC-1-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889430 181969 9 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at human CCR1 assessed as inhibition of HCC-1-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of HCC-1-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398726 181969 9 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at human CCR1 assessed as inhibition of HCC-1-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of HCC-1-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398728 181969 9 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at human CCR1 assessed as inhibition of HCC-1-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of HCC-1-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
21070989 177765 0 None None None Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None None None Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
57889180 233479 0 None None None Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334726 233479 0 None None None Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
57889897 181978 0 None None None Human 8.4 pIC50 = 8.4 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 456 6 2 3 4.2 CC(C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398737 181978 0 None None None Human 8.4 pIC50 = 8.4 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 456 6 2 3 4.2 CC(C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
24738063 181996 0 None None None Human 8.4 pIC50 = 8.4 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 419 5 1 3 4.1 CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CCN(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398758 181996 0 None None None Human 8.4 pIC50 = 8.4 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 419 5 1 3 4.1 CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CCN(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
44537841 1390 22 None None None Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]hMIP-1alpha from CCR1 in human PBMCDisplacement of [125I]hMIP-1alpha from CCR1 in human PBMC
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]hMIP-1alpha from CCR1 in human PBMCDisplacement of [125I]hMIP-1alpha from CCR1 in human PBMC
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]hMIP-1alpha from CCR1 in human PBMCDisplacement of [125I]hMIP-1alpha from CCR1 in human PBMC
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]hMIP-1alpha from CCR1 in human PBMCDisplacement of [125I]hMIP-1alpha from CCR1 in human PBMC
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]hMIP-1alpha from CCR1 in human PBMCDisplacement of [125I]hMIP-1alpha from CCR1 in human PBMC
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889979 181976 0 None None None Human 8.4 pIC50 = 8.4 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 443 5 2 4 3.6 CC(C)[C@@H](NC(=O)c1cccnc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398735 181976 0 None None None Human 8.4 pIC50 = 8.4 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 443 5 2 4 3.6 CC(C)[C@@H](NC(=O)c1cccnc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889121 181983 0 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 408 5 2 3 3.6 CC(C)C(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL2398742 181983 0 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 408 5 2 3 3.6 CC(C)C(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
57889003 181969 9 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at human CCR1 assessed as inhibition of ieukotactin-1-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of ieukotactin-1-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889430 181969 9 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at human CCR1 assessed as inhibition of ieukotactin-1-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of ieukotactin-1-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398726 181969 9 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at human CCR1 assessed as inhibition of ieukotactin-1-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of ieukotactin-1-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398728 181969 9 None None None Human 8.4 pIC50 = 8.4 Binding
Antagonist activity at human CCR1 assessed as inhibition of ieukotactin-1-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of ieukotactin-1-induced chemotaxis
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889843 181982 0 None None None Human 8.4 pIC50 = 8.4 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 394 5 2 3 3.3 CCC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL2398741 181982 0 None None None Human 8.4 pIC50 = 8.4 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 394 5 2 3 3.3 CCC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
72945310 214038 0 None None None Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 475 7 3 6 3.3 CNC(=O)Nc1ccc(OC)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.11.062
CHEMBL3099941 214038 0 None None None Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 475 7 3 6 3.3 CNC(=O)Nc1ccc(OC)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.11.062
57889121 181983 0 None None None Human 8.3 pIC50 = 8.3 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 408 5 2 3 3.6 CC(C)C(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL2398742 181983 0 None None None Human 8.3 pIC50 = 8.3 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 408 5 2 3 3.6 CC(C)C(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1016/j.bmcl.2013.04.079
57888747 182008 0 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1ccccc1Cl)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398770 182008 0 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1ccccc1Cl)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57888938 182004 0 None None None Human 7.4 pIC50 = 7.4 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 477 6 2 4 3.1 CC(C)[C@@H](NC(=O)c1cccc(S(N)(=O)=O)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2398766 182004 0 None None None Human 7.4 pIC50 = 7.4 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 477 6 2 4 3.1 CC(C)[C@@H](NC(=O)c1cccc(S(N)(=O)=O)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
57840427 177731 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 396 4 0 5 3.2 COc1cc(N2CCN(C(=O)Cn3nc(C)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322843 177731 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 396 4 0 5 3.2 COc1cc(N2CCN(C(=O)Cn3nc(C)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
24758294 164252 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 4.4 CC(C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
24758856 164252 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 4.4 CC(C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180496 164252 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 4.4 CC(C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180514 164252 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 4.4 CC(C)[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
24758171 164255 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 7 1 2 4.8 CC(C)[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
24759081 164255 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 7 1 2 4.8 CC(C)[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180499 164255 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 7 1 2 4.8 CC(C)[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180515 164255 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 7 1 2 4.8 CC(C)[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
10435088 181629 0 None None None Human 6.4 pIC50 = 6.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 475 8 4 7 1.9 NCCNC(=O)c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
CHEMBL2391936 181629 0 None None None Human 6.4 pIC50 = 6.4 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 475 8 4 7 1.9 NCCNC(=O)c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
44453579 311536 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 482 4 1 4 4.5 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL404465 311536 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 482 4 1 4 4.5 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
25233577 350734 0 None None None Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 419 4 1 2 5.0 Cc1cc(CN(C)C(=O)[C@H]2CCCN2C(=O)Nc2ccc(Cl)cc2)ccc1Cl 10.1021/jm801416q
CHEMBL460535 350734 0 None None None Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 419 4 1 2 5.0 Cc1cc(CN(C)C(=O)[C@H]2CCCN2C(=O)Nc2ccc(Cl)cc2)ccc1Cl 10.1021/jm801416q
59444242 334693 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 414 5 2 3 3.6 CC1(C)CN(C(=O)CCNC(=O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL4444092 334693 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 414 5 2 3 3.6 CC1(C)CN(C(=O)CCNC(=O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
44453437 316435 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)cc1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL411477 316435 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)cc1Cl 10.1016/j.bmcl.2007.09.068
44537841 1390 22 None None None Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at CCR1 receptor in human whole blood assessed as blocked of LKN1-mediated CD11b upregulation preincubated for 1 hrAntagonist activity at CCR1 receptor in human whole blood assessed as blocked of LKN1-mediated CD11b upregulation preincubated for 1 hr
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at CCR1 receptor in human whole blood assessed as blocked of LKN1-mediated CD11b upregulation preincubated for 1 hrAntagonist activity at CCR1 receptor in human whole blood assessed as blocked of LKN1-mediated CD11b upregulation preincubated for 1 hr
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at CCR1 receptor in human whole blood assessed as blocked of LKN1-mediated CD11b upregulation preincubated for 1 hrAntagonist activity at CCR1 receptor in human whole blood assessed as blocked of LKN1-mediated CD11b upregulation preincubated for 1 hr
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at CCR1 receptor in human whole blood assessed as blocked of LKN1-mediated CD11b upregulation preincubated for 1 hrAntagonist activity at CCR1 receptor in human whole blood assessed as blocked of LKN1-mediated CD11b upregulation preincubated for 1 hr
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 7.4 pIC50 = 7.4 Binding
Antagonist activity at CCR1 receptor in human whole blood assessed as blocked of LKN1-mediated CD11b upregulation preincubated for 1 hrAntagonist activity at CCR1 receptor in human whole blood assessed as blocked of LKN1-mediated CD11b upregulation preincubated for 1 hr
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
59444197 334654 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 420 5 2 3 3.7 CC(CNC(=O)C1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
CHEMBL4443458 334654 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 420 5 2 3 3.7 CC(CNC(=O)C1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
44430755 309540 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 577 10 2 8 3.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2cccnc2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL397910 309540 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 577 10 2 8 3.9 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2cccnc2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
71717437 177772 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 494 5 1 6 3.6 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(C(=O)O)c1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322882 177772 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 494 5 1 6 3.6 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(C(=O)O)c1Cl 10.1016/j.bmcl.2013.01.005
44453321 197795 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 502 4 1 4 4.8 O=S(=O)(c1c(Cl)cccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL270254 197795 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 502 4 1 4 4.8 O=S(=O)(c1c(Cl)cccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44309171 468989 0 None None None Human 6.4 pIC50 = 6.4 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 462 12 3 5 3.7 CC(C)CCC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.021
CHEMBL69816 468989 0 None None None Human 6.4 pIC50 = 6.4 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 462 12 3 5 3.7 CC(C)CCC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.021
9979012 161265 0 None None None Human 5.4 pIC50 = 5.4 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 411 7 1 5 4.4 O=C(CSc1nc2ccccc2s1)NCC1CCCN(Cc2ccccc2)C1 10.1016/s0960-894x(01)00176-7
CHEMBL21199 161265 0 None None None Human 5.4 pIC50 = 5.4 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 411 7 1 5 4.4 O=C(CSc1nc2ccccc2s1)NCC1CCCN(Cc2ccccc2)C1 10.1016/s0960-894x(01)00176-7
44453198 195981 0 None None None Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 516 4 1 4 5.2 CC1(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN(S(=O)(=O)c2c(Cl)cccc2Cl)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL257853 195981 0 None None None Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 516 4 1 4 5.2 CC1(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN(S(=O)(=O)c2c(Cl)cccc2Cl)CC1 10.1016/j.bmcl.2007.09.068
44309222 329022 0 None None None Human 5.4 pIC50 = 5.4 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 414 10 3 5 2.9 CC[C@H](C)[C@H](NC(=O)c1cnc2ccccc2n1)[C@@H](O)C[C@@H](CC(C)C)C(=O)NC 10.1016/j.bmcl.2004.02.021
CHEMBL420924 329022 0 None None None Human 5.4 pIC50 = 5.4 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 414 10 3 5 2.9 CC[C@H](C)[C@H](NC(=O)c1cnc2ccccc2n1)[C@@H](O)C[C@@H](CC(C)C)C(=O)NC 10.1016/j.bmcl.2004.02.021
57889002 164286 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 382 5 1 2 4.0 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(F)cc2)CC1 10.1021/jm300896d
CHEMBL2180533 164286 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 382 5 1 2 4.0 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(F)cc2)CC1 10.1021/jm300896d
59444291 348210 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 477 6 3 4 3.0 CC(=O)N[C@@H]1CC[C@@H](C(=O)N[C@H](C)CC(=O)N2CC[C@](O)(c3ccc(Cl)cc3)C(C)(C)C2)C1 nan
CHEMBL4546558 348210 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 477 6 3 4 3.0 CC(=O)N[C@@H]1CC[C@@H](C(=O)N[C@H](C)CC(=O)N2CC[C@](O)(c3ccc(Cl)cc3)C(C)(C)C2)C1 nan
44453199 196031 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 422 7 2 4 3.3 Cc1ccc(S(=O)(=O)NCCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL258064 196031 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 422 7 2 4 3.3 Cc1ccc(S(=O)(=O)NCCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1 10.1016/j.bmcl.2007.09.068
44453466 311588 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 486 4 1 4 4.3 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)c(F)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL404757 311588 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 486 4 1 4 4.3 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)c(F)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44453639 314727 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 482 4 1 4 4.4 Cc1cccc(Cl)c1S(=O)(=O)N1CCC[C@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
CHEMBL409498 314727 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 482 4 1 4 4.4 Cc1cccc(Cl)c1S(=O)(=O)N1CCC[C@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
25231302 350961 0 None None None Human 4.4 pIC50 = 4.4 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 435 6 2 3 4.0 O=C([C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1)N(CCO)Cc1ccccc1Cl 10.1021/jm801416q
CHEMBL462650 350961 0 None None None Human 4.4 pIC50 = 4.4 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 435 6 2 3 4.0 O=C([C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1)N(CCO)Cc1ccccc1Cl 10.1021/jm801416q
44431528 291925 0 None None None Human 7.4 pIC50 = 7.4 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 541 9 1 7 2.5 COS(=O)(=O)NC(=O)Cc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2007.03.037
CHEMBL391239 291925 0 None None None Human 7.4 pIC50 = 7.4 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 541 9 1 7 2.5 COS(=O)(=O)NC(=O)Cc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C 10.1016/j.bmcl.2007.03.037
24758517 164214 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 430 6 1 2 4.6 CC(C)[C@@H](NC(=O)Cc1cccc(F)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180187 164214 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 430 6 1 2 4.6 CC(C)[C@@H](NC(=O)Cc1cccc(F)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44453501 198109 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Br)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL271903 198109 0 None None None Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Br)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44309244 202162 0 None None None Human 4.4 pIC50 = 4.4 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 516 9 3 5 4.7 CC1(C)CC([C@H](C[C@H](O)[C@H](Cc2ccccc2)NC(=O)c2cnc3ccccc3n2)C(N)=O)CC(C)(C)C1 10.1016/j.bmcl.2004.02.021
CHEMBL302038 202162 0 None None None Human 4.4 pIC50 = 4.4 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 516 9 3 5 4.7 CC1(C)CC([C@H](C[C@H](O)[C@H](Cc2ccccc2)NC(=O)c2cnc3ccccc3n2)C(N)=O)CC(C)(C)C1 10.1016/j.bmcl.2004.02.021
24758518 163914 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 446 6 1 2 5.1 CC(C)[C@@H](NC(=O)Cc1cccc(Cl)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2177135 163914 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 446 6 1 2 5.1 CC(C)[C@@H](NC(=O)Cc1cccc(Cl)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57889478 164249 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 4.9 CC[C@@H](C)[C@@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180493 164249 0 None None None Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 6 1 2 4.9 CC[C@@H](C)[C@@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
70861827 350138 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 433 5 2 4 3.6 CC(C)(CC(=O)N1CCC(O)(c2ccc(C#N)cc2)C(C)(C)C1)NC(=O)c1ccccc1 nan
CHEMBL4593102 350138 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 433 5 2 4 3.6 CC(C)(CC(=O)N1CCC(O)(c2ccc(C#N)cc2)C(C)(C)C1)NC(=O)c1ccccc1 nan
11037958 157630 0 None None None Human 6.4 pIC50 = 6.4 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 465 6 1 5 5.5 O=C(CSc1nc2ccccc2s1)NC1CCN(Cc2ccc(Cl)c(Cl)c2)CC1 10.1021/jm300682j
CHEMBL20532 157630 0 None None None Human 6.4 pIC50 = 6.4 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 465 6 1 5 5.5 O=C(CSc1nc2ccccc2s1)NC1CCN(Cc2ccc(Cl)c(Cl)c2)CC1 10.1021/jm300682j
11037958 157630 0 None None None Human 6.4 pIC50 = 6.4 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 465 6 1 5 5.5 O=C(CSc1nc2ccccc2s1)NC1CCN(Cc2ccc(Cl)c(Cl)c2)CC1 10.1016/s0960-894x(01)00176-7
CHEMBL20532 157630 0 None None None Human 6.4 pIC50 = 6.4 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 465 6 1 5 5.5 O=C(CSc1nc2ccccc2s1)NC1CCN(Cc2ccc(Cl)c(Cl)c2)CC1 10.1016/s0960-894x(01)00176-7
57889003 181969 9 None None None Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of MIP1alpha-induced upregulation of beta2-integrin CD11bAntagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of MIP1alpha-induced upregulation of beta2-integrin CD11b
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889430 181969 9 None None None Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of MIP1alpha-induced upregulation of beta2-integrin CD11bAntagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of MIP1alpha-induced upregulation of beta2-integrin CD11b
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398726 181969 9 None None None Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of MIP1alpha-induced upregulation of beta2-integrin CD11bAntagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of MIP1alpha-induced upregulation of beta2-integrin CD11b
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398728 181969 9 None None None Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of MIP1alpha-induced upregulation of beta2-integrin CD11bAntagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of MIP1alpha-induced upregulation of beta2-integrin CD11b
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57888690 164259 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 376 6 1 2 4.0 CC(C)[C@@H](NC(=O)CC1CC1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180503 164259 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 376 6 1 2 4.0 CC(C)[C@@H](NC(=O)CC1CC1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
3497 2447 26 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2004.02.022
44309353 2447 26 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2004.02.022
5311123 2447 26 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2004.02.022
CHEMBL1628706 2447 26 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2004.02.022
CHEMBL308473 2447 26 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1016/j.bmcl.2004.02.022
59444274 350110 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 535 6 3 5 4.4 C[C@H](CC(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)NC(=O)[C@@H]1CC[C@@H](NC(=O)OC(C)(C)C)C1 nan
CHEMBL4592423 350110 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 535 6 3 5 4.4 C[C@H](CC(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)NC(=O)[C@@H]1CC[C@@H](NC(=O)OC(C)(C)C)C1 nan
44453615 195538 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Br)N1CCC[C@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
CHEMBL255797 195538 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Br)N1CCC[C@H](N2CCC(O)(c3ccc(Cl)cc3)CC2)C1 10.1016/j.bmcl.2007.09.068
44309128 468981 0 None None None Human 5.3 pIC50 = 5.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 422 10 4 6 1.2 NC(=O)[C@H](CCO)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
CHEMBL69735 468981 0 None None None Human 5.3 pIC50 = 5.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 422 10 4 6 1.2 NC(=O)[C@H](CCO)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
57840515 177759 1 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 493 6 0 6 3.6 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3CN(C)C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322869 177759 1 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 493 6 0 6 3.6 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3CN(C)C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
6918497 232475 1 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
CHEMBL331897 232475 1 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
25233578 373173 0 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 419 4 1 2 5.2 CC(c1ccc(Cl)cc1)N(C)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1 10.1021/jm801416q
CHEMBL517262 373173 0 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 419 4 1 2 5.2 CC(c1ccc(Cl)cc1)N(C)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1 10.1021/jm801416q
57889613 182000 0 None None None Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 432 5 2 3 4.3 CC(C)[C@@H](NC(=O)c1ccc(F)c(O)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2398762 182000 0 None None None Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 432 5 2 3 4.3 CC(C)[C@@H](NC(=O)c1ccc(F)c(O)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
57889023 182003 0 None None None Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 576 7 4 4 5.4 CC(C)[C@@H](NC(=O)c1cccc(-c2ccccc2NC(N)=O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398765 182003 0 None None None Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 576 7 4 4 5.4 CC(C)[C@@H](NC(=O)c1cccc(-c2ccccc2NC(N)=O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
44309318 203041 0 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 460 10 3 5 3.4 NC(=O)[C@H](CC1CCCC1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
CHEMBL306685 203041 0 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 460 10 3 5 3.4 NC(=O)[C@H](CC1CCCC1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
9889700 237386 15 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 444 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0004244
CHEMBL34166 237386 15 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 444 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0004244
44431523 178924 0 None None None Human 6.3 pIC50 = 6.3 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 468 11 4 6 3.0 CC(C)(O)CC[C@@H](CN)C[C@H](O)[C@H](Cc1cccc(F)c1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2007.03.037
CHEMBL234606 178924 0 None None None Human 6.3 pIC50 = 6.3 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 468 11 4 6 3.0 CC(C)(O)CC[C@@H](CN)C[C@H](O)[C@H](Cc1cccc(F)c1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2007.03.037
602123 174772 48 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 236 2 0 4 2.4 O=Cc1ccc2ccc3ccc(C=O)nc3c2n1 10.1021/jm301121j
CHEMBL2205803 174772 48 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 236 2 0 4 2.4 O=Cc1ccc2ccc3ccc(C=O)nc3c2n1 10.1021/jm301121j
68962095 181597 0 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 500 6 2 6 3.1 Cc1ccc(C(=O)N2CC[C@H](O)C2)c(OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)c1 10.1016/j.bmcl.2013.04.047
CHEMBL2391799 181597 0 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 500 6 2 6 3.1 Cc1ccc(C(=O)N2CC[C@H](O)C2)c(OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)c1 10.1016/j.bmcl.2013.04.047
57840437 177747 0 None None None Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 434 4 0 5 3.4 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(F)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322858 177747 0 None None None Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 434 4 0 5 3.4 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(F)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
71717436 177769 0 None None None Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 468 4 0 5 4.0 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(F)c1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322879 177769 0 None None None Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 468 4 0 5 4.0 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(F)c1Cl 10.1016/j.bmcl.2013.01.005
10579693 25448 0 None None None Human 8.3 pIC50 = 8.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 489 7 1 2 7.2 CCCC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178558 25448 0 None None None Human 8.3 pIC50 = 8.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 489 7 1 2 7.2 CCCC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
44537841 1390 22 None None None Human 8.3 pIC50 = 8.3 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2013.04.079
57889181 1390 22 None None None Human 8.3 pIC50 = 8.3 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2013.04.079
9497 1390 22 None None None Human 8.3 pIC50 = 8.3 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL2398716 1390 22 None None None Human 8.3 pIC50 = 8.3 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2013.04.079
CHEMBL3334824 1390 22 None None None Human 8.3 pIC50 = 8.3 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1016/j.bmcl.2013.04.079
9894714 26260 0 None None None Human 8.3 pIC50 = 8.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 461 5 1 2 6.4 CC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1183117 26260 0 None None None Human 8.3 pIC50 = 8.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 461 5 1 2 6.4 CC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
52916803 335526 28 None None None Human 8.3 pIC50 = 8.3 Binding
Affinity Biochemical interaction (Scintillation Proximity Assay (SPA)) EUB0000352a CCR1Affinity Biochemical interaction (Scintillation Proximity Assay (SPA)) EUB0000352a CCR1
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL5210307
CHEMBL4456123 335526 28 None None None Human 8.3 pIC50 = 8.3 Binding
Affinity Biochemical interaction (Scintillation Proximity Assay (SPA)) EUB0000352a CCR1Affinity Biochemical interaction (Scintillation Proximity Assay (SPA)) EUB0000352a CCR1
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL5210307
52916803 335526 28 None None None Human 8.3 pIC50 = 8.3 Binding
Scintillation Proximity Assay bindingScintillation Proximity Assay binding
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL4507278
CHEMBL4456123 335526 28 None None None Human 8.3 pIC50 = 8.3 Binding
Scintillation Proximity Assay bindingScintillation Proximity Assay binding
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL4507278
44537841 1390 22 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57888895 181971 0 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1ccc(Cl)cc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398730 181971 0 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1ccc(Cl)cc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
512282 1562 44 None None None Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm801416q
767 1562 44 None None None Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm801416q
CHEMBL232656 1562 44 None None None Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm801416q
71681399 181967 0 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CCC[C@@H]1N)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398724 181967 0 None None None Human 8.3 pIC50 = 8.3 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 449 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CCC[C@@H]1N)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
10482996 214047 0 None None None Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 449 6 3 5 3.2 NC(=O)Nc1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.11.062
CHEMBL3099950 214047 0 None None None Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 449 6 3 5 3.2 NC(=O)Nc1ccc(F)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.11.062
57889758 181979 0 None None None Human 8.2 pIC50 = 8.2 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 470 7 2 3 4.6 CC(C)[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398738 181979 0 None None None Human 8.2 pIC50 = 8.2 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 470 7 2 3 4.6 CC(C)[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
6918497 232475 1 None None None Mouse 8.2 pIC50 = 8.2 Binding
Inhibitory activity against 125 I -MIP-1 alpha binding to mouse CCR1 receptorsInhibitory activity against 125 I -MIP-1 alpha binding to mouse CCR1 receptors
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
CHEMBL331897 232475 1 None None None Mouse 8.2 pIC50 = 8.2 Binding
Inhibitory activity against 125 I -MIP-1 alpha binding to mouse CCR1 receptorsInhibitory activity against 125 I -MIP-1 alpha binding to mouse CCR1 receptors
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
6918497 232475 1 None None None Mouse 8.2 pIC50 = 8.2 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
CHEMBL331897 232475 1 None None None Mouse 8.2 pIC50 = 8.2 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
11236656 177758 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 465 5 1 6 3.0 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3CN)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322868 177758 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 465 5 1 6 3.0 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3CN)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
24782574 353253 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 453 4 1 2 5.3 Cc1cc(C(F)(F)F)ccc1NC(=O)N1CCC[C@@H]1C(=O)N(C)Cc1ccc(Cl)cc1 10.1021/jm801416q
CHEMBL473734 353253 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 453 4 1 2 5.3 Cc1cc(C(F)(F)F)ccc1NC(=O)N1CCC[C@@H]1C(=O)N(C)Cc1ccc(Cl)cc1 10.1021/jm801416q
24758744 164251 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 6 1 2 4.2 CC[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180495 164251 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 6 1 2 4.2 CC[C@@H](NC(=O)Cc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44430753 279194 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 598 11 3 9 2.2 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCNCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL387608 279194 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 598 11 3 9 2.2 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCNCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
57840557 177752 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 473 5 1 6 3.2 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(NC(C)=O)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322862 177752 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 473 5 1 6 3.2 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(NC(C)=O)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
44453292 311437 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 448 4 1 4 3.8 Cc1ccccc1S(=O)(=O)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL404033 311437 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 448 4 1 4 3.8 Cc1ccccc1S(=O)(=O)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
11072275 40680 0 None None None Human 6.3 pIC50 = 6.3 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 632 10 3 5 5.9 COC(=O)N1CCC(NC(=O)NCC(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)(c2ccccc2)c2ccccc2)CC1 10.1021/jm0201767
CHEMBL124585 40680 0 None None None Human 6.3 pIC50 = 6.3 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 632 10 3 5 5.9 COC(=O)N1CCC(NC(=O)NCC(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)(c2ccccc2)c2ccccc2)CC1 10.1021/jm0201767
9889700 237386 15 None None None Mouse 5.3 pIC50 = 5.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 444 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0004244
CHEMBL34166 237386 15 None None None Mouse 5.3 pIC50 = 5.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 444 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0004244
602123 174772 48 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 236 2 0 4 2.4 O=Cc1ccc2ccc3ccc(C=O)nc3c2n1 10.1021/jm301121j
CHEMBL2205803 174772 48 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 236 2 0 4 2.4 O=Cc1ccc2ccc3ccc(C=O)nc3c2n1 10.1021/jm301121j
77865 216919 57 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 214 0 0 2 3.4 Clc1cc2cccnc2c2ncccc12 10.1021/jm301121j
CHEMBL317115 216919 57 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 214 0 0 2 3.4 Clc1cc2cccnc2c2ncccc12 10.1021/jm301121j
10670301 233135 0 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 430 4 1 3 5.8 O=C(NC1CCN(C/C2=C/CCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
CHEMBL33277 233135 0 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 430 4 1 3 5.8 O=C(NC1CCN(C/C2=C/CCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
44453469 196095 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(Cl)c1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL258360 196095 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(Cl)c1Cl 10.1016/j.bmcl.2007.09.068
44453499 311371 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 486 4 1 4 4.3 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(F)c(Cl)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL403613 311371 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 486 4 1 4 4.3 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(F)c(Cl)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44309236 468643 0 None None None Human 6.3 pIC50 = 6.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 475 10 3 4 3.3 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cncc(Br)c1 10.1016/j.bmcl.2004.02.021
CHEMBL67256 468643 0 None None None Human 6.3 pIC50 = 6.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 475 10 3 4 3.3 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cncc(Br)c1 10.1016/j.bmcl.2004.02.021
11794863 237676 0 None None None Human 6.3 pIC50 = 6.3 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 392 7 1 3 5.1 CCCCCCN1CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1016/j.ejmech.2020.113085
CHEMBL34226 237676 0 None None None Human 6.3 pIC50 = 6.3 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 392 7 1 3 5.1 CCCCCCN1CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1016/j.ejmech.2020.113085
11794863 237676 0 None None None Human 6.3 pIC50 = 6.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 392 7 1 3 5.1 CCCCCCN1CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL34226 237676 0 None None None Human 6.3 pIC50 = 6.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 392 7 1 3 5.1 CCCCCCN1CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
77865 216919 57 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 214 0 0 2 3.4 Clc1cc2cccnc2c2ncccc12 10.1021/jm301121j
CHEMBL317115 216919 57 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 214 0 0 2 3.4 Clc1cc2cccnc2c2ncccc12 10.1021/jm301121j
10793529 219313 0 None None None Human 5.3 pIC50 = 5.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 588 4 1 3 7.4 O=C(NC1CCN(CC2CCCCCCC2)CC1)C1c2cc(Br)ccc2Oc2ccc(Br)cc21 10.1021/jm0004244
CHEMBL32305 219313 0 None None None Human 5.3 pIC50 = 5.3 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 588 4 1 3 7.4 O=C(NC1CCN(CC2CCCCCCC2)CC1)C1c2cc(Br)ccc2Oc2ccc(Br)cc21 10.1021/jm0004244
44453197 311380 0 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 482 4 1 4 4.5 CC1(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN(S(=O)(=O)c2ccccc2Cl)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL403665 311380 0 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 482 4 1 4 4.5 CC1(N2CCC(O)(c3ccc(Cl)cc3)CC2)CCN(S(=O)(=O)c2ccccc2Cl)CC1 10.1016/j.bmcl.2007.09.068
44309112 468910 0 None None None Human 5.3 pIC50 = 5.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cncc2ccccc12 10.1016/j.bmcl.2004.02.021
CHEMBL69285 468910 0 None None None Human 5.3 pIC50 = 5.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cncc2ccccc12 10.1016/j.bmcl.2004.02.021
71719856 177773 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 493 5 1 6 3.0 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(C(N)=O)c1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322883 177773 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 493 5 1 6 3.0 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc(C(N)=O)c1Cl 10.1016/j.bmcl.2013.01.005
44309313 202594 0 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 482 11 4 6 2.5 CC(C)(O)CCC(C[C@H](O)[C@H](Cc1ccccc1F)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
CHEMBL304053 202594 0 None None None Human 7.3 pIC50 = 7.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 482 11 4 6 2.5 CC(C)(O)CCC(C[C@H](O)[C@H](Cc1ccccc1F)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
57840210 177740 0 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 5 1 6 2.6 COc1cc(N2CCN(C(=O)Cn3nc(C(=O)O)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322851 177740 0 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 5 1 6 2.6 COc1cc(N2CCN(C(=O)Cn3nc(C(=O)O)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
57889880 164300 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 414 6 2 3 3.7 CCCC(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180549 164300 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 414 6 2 3 3.7 CCCC(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
24740167 164287 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 399 5 1 3 3.4 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CCN(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180535 164287 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 399 5 1 3 3.4 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CCN(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57889006 164302 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 446 7 2 4 3.7 CSCCC(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180551 164302 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 446 7 2 4 3.7 CSCCC(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57889003 181969 9 None None None Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of LKN1-induced upregulation of beta2-integrin CD11bAntagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of LKN1-induced upregulation of beta2-integrin CD11b
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889430 181969 9 None None None Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of LKN1-induced upregulation of beta2-integrin CD11bAntagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of LKN1-induced upregulation of beta2-integrin CD11b
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398726 181969 9 None None None Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of LKN1-induced upregulation of beta2-integrin CD11bAntagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of LKN1-induced upregulation of beta2-integrin CD11b
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398728 181969 9 None None None Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of LKN1-induced upregulation of beta2-integrin CD11bAntagonist activity at CCR1 in whole blood (unknown origin) assessed as inhibition of LKN1-induced upregulation of beta2-integrin CD11b
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
25233947 348330 5 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 435 6 2 3 4.0 O=C([C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1)N(CCO)Cc1ccc(Cl)cc1 10.1021/jm801416q
CHEMBL454940 348330 5 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 435 6 2 3 4.0 O=C([C@H]1CCCN1C(=O)Nc1ccc(Cl)cc1)N(CCO)Cc1ccc(Cl)cc1 10.1021/jm801416q
44453435 197904 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cc(Cl)ccc1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL270863 197904 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cc(Cl)ccc1Cl 10.1016/j.bmcl.2007.09.068
44309407 203014 0 None None None Human 6.3 pIC50 = 6.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 476 9 4 6 2.5 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1(O)CCCCC1 10.1016/j.bmcl.2004.02.022
CHEMBL306457 203014 0 None None None Human 6.3 pIC50 = 6.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 476 9 4 6 2.5 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1(O)CCCCC1 10.1016/j.bmcl.2004.02.022
57889346 164276 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 441 7 2 2 4.6 CC(C)[C@@H](NC(=O)NCCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180522 164276 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 441 7 2 2 4.6 CC(C)[C@@H](NC(=O)NCCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
24758044 164277 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57888953 164277 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
71455572 164277 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180523 164277 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180528 164277 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180534 164277 0 None None None Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
24758044 164277 0 None None None Rabbit 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in rabbit PBMCs incubated for 60 minsDisplacement of [125I]MIP-1alpha from CCR1 in rabbit PBMCs incubated for 60 mins
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
57888953 164277 0 None None None Rabbit 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in rabbit PBMCs incubated for 60 minsDisplacement of [125I]MIP-1alpha from CCR1 in rabbit PBMCs incubated for 60 mins
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
71455572 164277 0 None None None Rabbit 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in rabbit PBMCs incubated for 60 minsDisplacement of [125I]MIP-1alpha from CCR1 in rabbit PBMCs incubated for 60 mins
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180523 164277 0 None None None Rabbit 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in rabbit PBMCs incubated for 60 minsDisplacement of [125I]MIP-1alpha from CCR1 in rabbit PBMCs incubated for 60 mins
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180528 164277 0 None None None Rabbit 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in rabbit PBMCs incubated for 60 minsDisplacement of [125I]MIP-1alpha from CCR1 in rabbit PBMCs incubated for 60 mins
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180534 164277 0 None None None Rabbit 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from CCR1 in rabbit PBMCs incubated for 60 minsDisplacement of [125I]MIP-1alpha from CCR1 in rabbit PBMCs incubated for 60 mins
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44309061 328574 0 None None None Human 4.3 pIC50 = 4.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 449 11 3 6 1.8 CN(C)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.021
CHEMBL420359 328574 0 None None None Human 4.3 pIC50 = 4.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 449 11 3 6 1.8 CN(C)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.021
69437285 214051 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 457 5 3 6 2.1 O=c1[nH]c(=O)c2cccc(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)c2[nH]1 10.1016/j.bmcl.2013.11.062
CHEMBL3099954 214051 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 457 5 3 6 2.1 O=c1[nH]c(=O)c2cccc(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)c2[nH]1 10.1016/j.bmcl.2013.11.062
68816399 214056 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 423 5 2 5 2.8 N[C@H](COc1cccc2ccc(=O)[nH]c12)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2013.11.062
CHEMBL3099959 214056 0 None None None Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 423 5 2 5 2.8 N[C@H](COc1cccc2ccc(=O)[nH]c12)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2013.11.062
44309219 202205 0 None None None Human 6.3 pIC50 = 6.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 512 9 4 6 2.8 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1(O)CCC(F)(F)CC1 10.1016/j.bmcl.2004.02.022
CHEMBL302320 202205 0 None None None Human 6.3 pIC50 = 6.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 512 9 4 6 2.8 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1(O)CCC(F)(F)CC1 10.1016/j.bmcl.2004.02.022
21071066 177779 0 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 386 3 0 4 3.2 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccccc2)CC1 10.1016/j.bmcl.2013.01.005
CHEMBL2322889 177779 0 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 386 3 0 4 3.2 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccccc2)CC1 10.1016/j.bmcl.2013.01.005
44309077 469245 0 None None None Human 5.3 pIC50 = 5.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 549 11 2 6 3.6 CN1CCN(C(=O)C(CCC(C)(C)F)C[C@H](O)[C@H](Cc2ccccc2)NC(=O)c2cnc3ccccc3n2)CC1 10.1016/j.bmcl.2004.02.022
CHEMBL71499 469245 0 None None None Human 5.3 pIC50 = 5.3 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 549 11 2 6 3.6 CN1CCN(C(=O)C(CCC(C)(C)F)C[C@H](O)[C@H](Cc2ccccc2)NC(=O)c2cnc3ccccc3n2)CC1 10.1016/j.bmcl.2004.02.022
21071098 177826 0 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 431 4 0 6 3.1 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc([N+](=O)[O-])cc2)CC1 10.1016/j.bmcl.2013.01.005
CHEMBL2323420 177826 0 None None None Human 5.3 pIC50 = 5.3 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 431 4 0 6 3.1 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc([N+](=O)[O-])cc2)CC1 10.1016/j.bmcl.2013.01.005
44453528 197843 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 414 7 2 5 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccsc1 10.1016/j.bmcl.2007.09.068
CHEMBL270564 197843 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 414 7 2 5 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccsc1 10.1016/j.bmcl.2007.09.068
25231481 350960 0 None None None Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 385 4 1 2 4.3 Cc1ccc(CN(C)C(=O)[C@H]2CCCN2C(=O)Nc2ccc(Cl)cc2)cc1 10.1021/jm801416q
CHEMBL462644 350960 0 None None None Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 385 4 1 2 4.3 Cc1ccc(CN(C)C(=O)[C@H]2CCCN2C(=O)Nc2ccc(Cl)cc2)cc1 10.1021/jm801416q
24758175 164223 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 454 5 1 3 5.7 CC(C)[C@@H](NC(=O)c1cc2ccccc2s1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180196 164223 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 454 5 1 3 5.7 CC(C)[C@@H](NC(=O)c1cc2ccccc2s1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44453228 195769 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 426 7 2 4 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1F 10.1016/j.bmcl.2007.09.068
CHEMBL256888 195769 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 426 7 2 4 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1F 10.1016/j.bmcl.2007.09.068
44309235 202206 0 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1nccc2ccccc12 10.1016/j.bmcl.2004.02.021
CHEMBL302328 202206 0 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1nccc2ccccc12 10.1016/j.bmcl.2004.02.021
44309194 468546 0 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 464 11 4 6 2.4 CC(C)(O)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
CHEMBL66457 468546 0 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 464 11 4 6 2.4 CC(C)(O)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
25174628 258178 0 None None None Human 6.2 pIC50 = 6.2 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 498 5 3 4 4.2 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)[C@H](O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
25174629 258178 0 None None None Human 6.2 pIC50 = 6.2 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 498 5 3 4 4.2 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)[C@H](O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679648 258178 0 None None None Human 6.2 pIC50 = 6.2 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 498 5 3 4 4.2 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)[C@H](O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679649 258178 0 None None None Human 6.2 pIC50 = 6.2 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 498 5 3 4 4.2 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)[C@H](O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
44453084 195641 0 None None None Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 422 6 2 3 4.6 O=C(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc2ccccc2c1 10.1016/j.bmcl.2007.09.068
CHEMBL256264 195641 0 None None None Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 422 6 2 3 4.6 O=C(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc2ccccc2c1 10.1016/j.bmcl.2007.09.068
11166434 292014 0 None None None Human 7.2 pIC50 = 7.2 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 434 6 1 4 3.7 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2C(=O)O)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
CHEMBL391301 292014 0 None None None Human 7.2 pIC50 = 7.2 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 434 6 1 4 3.7 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2C(=O)O)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
10670301 233135 0 None None None Mouse 6.2 pIC50 = 6.2 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 430 4 1 3 5.8 O=C(NC1CCN(C/C2=C/CCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
CHEMBL33277 233135 0 None None None Mouse 6.2 pIC50 = 6.2 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 430 4 1 3 5.8 O=C(NC1CCN(C/C2=C/CCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
44537841 1390 22 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57888785 233482 0 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334815 233482 0 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 465 5 4 4 3.0 CC(C)[C@@H](NC(=O)N[C@H]1CC[C@@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
57889188 233483 0 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 437 6 3 3 3.9 CC[C@@H](C)NC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1021/jm5003167
CHEMBL3334816 233483 0 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 437 6 3 3 3.9 CC[C@@H](C)NC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C 10.1021/jm5003167
118714037 233490 0 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 439 6 4 4 2.5 CC(C)[C@@H](NC(=O)NC[C@@H](C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334823 233490 0 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 439 6 4 4 2.5 CC(C)[C@@H](NC(=O)NC[C@@H](C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
57840302 177751 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 441 4 0 6 3.1 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(C#N)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322861 177751 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 441 4 0 6 3.1 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(C#N)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
21070989 177765 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human monocytesDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human monocytes
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human monocytesDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human monocytes
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
11397004 178228 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 459 7 2 6 3.5 COc1ccc(NC(C)=O)c(OC[C@@H](N)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)c1 10.1016/j.bmcl.2012.12.095
CHEMBL2332937 178228 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 459 7 2 6 3.5 COc1ccc(NC(C)=O)c(OC[C@@H](N)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)c1 10.1016/j.bmcl.2012.12.095
57889979 181976 0 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 443 5 2 4 3.6 CC(C)[C@@H](NC(=O)c1cccnc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398735 181976 0 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 443 5 2 4 3.6 CC(C)[C@@H](NC(=O)c1cccnc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57888919 181970 0 None None None Human 8.2 pIC50 = 8.2 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57889974 181970 0 None None None Human 8.2 pIC50 = 8.2 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398727 181970 0 None None None Human 8.2 pIC50 = 8.2 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398729 181970 0 None None None Human 8.2 pIC50 = 8.2 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 450 5 3 4 3.1 CC(C)[C@@H](NC(=O)[C@H]1CC[C@H](O)C1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57888747 182008 0 None None None Human 8.2 pIC50 = 8.2 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1ccccc1Cl)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398770 182008 0 None None None Human 8.2 pIC50 = 8.2 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1ccccc1Cl)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
10030344 214046 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 431 6 3 5 3.0 NC(=O)Nc1ccccc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.11.062
CHEMBL3099949 214046 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 431 6 3 5 3.0 NC(=O)Nc1ccccc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.11.062
57889484 182002 0 None None None Human 8.2 pIC50 = 8.2 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 532 7 3 3 5.7 CC(C)[C@@H](NC(=O)c1cccc(-c2ccccc2NC(N)=O)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2398764 182002 0 None None None Human 8.2 pIC50 = 8.2 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 532 7 3 3 5.7 CC(C)[C@@H](NC(=O)c1cccc(-c2ccccc2NC(N)=O)c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
44453584 198222 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 484 8 2 4 4.7 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1-c1ccccc1 10.1016/j.bmcl.2007.09.068
CHEMBL272523 198222 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 484 8 2 4 4.7 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1-c1ccccc1 10.1016/j.bmcl.2007.09.068
44453557 311501 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 451 7 1 4 4.2 N#CC1(c2ccc(Cl)cc2)CCN(CCCNS(=O)(=O)c2ccccc2Cl)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL404301 311501 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 451 7 1 4 4.2 N#CC1(c2ccc(Cl)cc2)CCN(CCCNS(=O)(=O)c2ccccc2Cl)CC1 10.1016/j.bmcl.2007.09.068
44309192 203231 0 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 464 10 4 6 2.8 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccc(O)cc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
CHEMBL308209 203231 0 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 464 10 4 6 2.8 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccc(O)cc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
512282 1562 44 None None None Mouse 6.2 pIC50 = 6.2 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2007.03.104
767 1562 44 None None None Mouse 6.2 pIC50 = 6.2 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2007.03.104
CHEMBL232656 1562 44 None None None Mouse 6.2 pIC50 = 6.2 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1016/j.bmcl.2007.03.104
44430713 177592 0 None None None Mouse 6.2 pIC50 = 6.2 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 500 8 2 7 3.0 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL231829 177592 0 None None None Mouse 6.2 pIC50 = 6.2 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 500 8 2 7 3.0 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
57888949 164274 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 413 5 2 2 4.9 CC(C)[C@@H](NC(=O)Nc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180520 164274 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 413 5 2 2 4.9 CC(C)[C@@H](NC(=O)Nc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44430745 279221 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 544 11 2 8 3.0 COCCNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL387822 279221 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 544 11 2 8 3.0 COCCNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
10698568 25460 0 None None None Mouse 7.2 pIC50 = 7.2 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 459 5 1 2 6.3 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178613 25460 0 None None None Mouse 7.2 pIC50 = 7.2 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 459 5 1 2 6.3 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
9889700 237386 15 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 444 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
CHEMBL34166 237386 15 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 444 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
44537841 1390 22 None None None Dog 6.2 pIC50 = 6.2 Binding
Displacement of [125I]hMIP-1alpha from dog PBMC CCR1Displacement of [125I]hMIP-1alpha from dog PBMC CCR1
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Dog 6.2 pIC50 = 6.2 Binding
Displacement of [125I]hMIP-1alpha from dog PBMC CCR1Displacement of [125I]hMIP-1alpha from dog PBMC CCR1
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Dog 6.2 pIC50 = 6.2 Binding
Displacement of [125I]hMIP-1alpha from dog PBMC CCR1Displacement of [125I]hMIP-1alpha from dog PBMC CCR1
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Dog 6.2 pIC50 = 6.2 Binding
Displacement of [125I]hMIP-1alpha from dog PBMC CCR1Displacement of [125I]hMIP-1alpha from dog PBMC CCR1
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Dog 6.2 pIC50 = 6.2 Binding
Displacement of [125I]hMIP-1alpha from dog PBMC CCR1Displacement of [125I]hMIP-1alpha from dog PBMC CCR1
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
44430750 178130 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 583 11 2 8 3.4 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL233042 178130 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 583 11 2 8 3.4 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN2CCCC2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44309074 468824 0 None None None Human 7.2 pIC50 = 7.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 448 10 3 5 3.1 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
CHEMBL68581 468824 0 None None None Human 7.2 pIC50 = 7.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 448 10 3 5 3.1 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
58778007 177827 0 None None None Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 4 0 6 2.6 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(S(C)(=O)=O)cc2)CC1 10.1016/j.bmcl.2013.01.005
CHEMBL2323421 177827 0 None None None Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 4 0 6 2.6 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(S(C)(=O)=O)cc2)CC1 10.1016/j.bmcl.2013.01.005
49865900 40073 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 448 4 1 3 6.0 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCCC1c1nccn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
CHEMBL1224118 40073 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 448 4 1 3 6.0 O=C(Nc1ccc(C(F)(F)F)cc1)N1CCCC1c1nccn1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
10049290 468931 0 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
10049290 468931 0 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.021
CHEMBL69411 468931 0 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.020
CHEMBL69411 468931 0 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 447 10 3 4 3.7 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2c1 10.1016/j.bmcl.2004.02.021
71453837 164256 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 440 8 1 2 5.2 CC[C@@H](C)[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180500 164256 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 440 8 1 2 5.2 CC[C@@H](C)[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
9894714 26260 0 None None None Mouse 6.2 pIC50 = 6.2 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 461 5 1 2 6.4 CC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1183117 26260 0 None None None Mouse 6.2 pIC50 = 6.2 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 461 5 1 2 6.4 CC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
11813735 236969 0 None None None Human 7.2 pIC50 = 7.2 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 562 12 3 4 5.3 CN(C)CCNC(=O)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
CHEMBL340797 236969 0 None None None Human 7.2 pIC50 = 7.2 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 562 12 3 4 5.3 CN(C)CCNC(=O)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
44309185 469298 0 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 454 10 3 5 3.9 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
CHEMBL71903 469298 0 None None None Human 6.2 pIC50 = 6.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 454 10 3 5 3.9 CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.021
10555551 25450 0 None None None Mouse 6.2 pIC50 = 6.2 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 473 6 1 2 6.6 C=CC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178575 25450 0 None None None Mouse 6.2 pIC50 = 6.2 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 473 6 1 2 6.6 C=CC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
71570634 178233 0 None None None Human 7.2 pIC50 = 7.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 411 6 3 6 2.5 CC(=O)Nc1ccc(O)cc1OC[C@@H](N)CN1CCC2(CC1)Cc1ccccc1O2 10.1016/j.bmcl.2012.12.095
CHEMBL2332942 178233 0 None None None Human 7.2 pIC50 = 7.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 411 6 3 6 2.5 CC(=O)Nc1ccc(O)cc1OC[C@@H](N)CN1CCC2(CC1)Cc1ccccc1O2 10.1016/j.bmcl.2012.12.095
57840380 177760 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 507 6 1 6 3.2 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3CNC(C)=O)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322870 177760 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 507 6 1 6 3.2 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3CNC(C)=O)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
25233579 350838 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 385 4 1 2 4.3 Cc1ccc(NC(=O)N2CCC[C@@H]2C(=O)N(C)Cc2ccc(Cl)cc2)cc1 10.1021/jm801416q
CHEMBL461590 350838 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 385 4 1 2 4.3 Cc1ccc(NC(=O)N2CCC[C@@H]2C(=O)N(C)Cc2ccc(Cl)cc2)cc1 10.1021/jm801416q
44453363 197829 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 458 7 2 4 4.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc2ccccc12 10.1016/j.bmcl.2007.09.068
CHEMBL270433 197829 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 458 7 2 4 4.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc2ccccc12 10.1016/j.bmcl.2007.09.068
49865951 40089 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 463 4 1 4 5.7 Cc1nnc([C@H]2CCCN2C(=O)Nc2ccc(C(F)(F)F)cc2)n1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
CHEMBL1224189 40089 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 463 4 1 4 5.7 Cc1nnc([C@H]2CCCN2C(=O)Nc2ccc(C(F)(F)F)cc2)n1Cc1ccc(Cl)cc1 10.1016/j.bmcl.2010.07.082
118714035 233488 0 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 439 6 4 4 2.5 CC(C)[C@@H](NC(=O)NC[C@H](C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334821 233488 0 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MIP-1alpha induced chemotaxis after 60 mins
ChEMBL 439 6 4 4 2.5 CC(C)[C@@H](NC(=O)NC[C@H](C)O)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
57840482 177750 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 542 4 0 5 3.8 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(I)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322860 177750 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 542 4 0 5 3.8 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(I)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
44430758 279954 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 482 6 2 6 3.1 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1Nc1c(N)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL389293 279954 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 482 6 2 6 3.1 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)/C=C/c1ccc(Cl)cc1Nc1c(N)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44309286 202416 0 None None None Human 8.2 pIC50 = 8.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 512 9 4 6 3.7 O=C(N[C@@H](Cc1ccccc1)[C@@H](O)CC(C(=O)NO)C1CCC(F)(F)CC1)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.022
CHEMBL303673 202416 0 None None None Human 8.2 pIC50 = 8.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 512 9 4 6 3.7 O=C(N[C@@H](Cc1ccccc1)[C@@H](O)CC(C(=O)NO)C1CCC(F)(F)CC1)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.022
44309143 468504 0 None None None Human 8.2 pIC50 = 8.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 481 11 4 6 2.9 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)NN 10.1016/j.bmcl.2004.02.022
CHEMBL66159 468504 0 None None None Human 8.2 pIC50 = 8.2 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 481 11 4 6 2.9 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)NN 10.1016/j.bmcl.2004.02.022
68956901 181607 0 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 500 6 2 6 3.9 O=C(c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CCCCC1 10.1016/j.bmcl.2013.04.047
CHEMBL2391809 181607 0 None None None Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 500 6 2 6 3.9 O=C(c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CCCCC1 10.1016/j.bmcl.2013.04.047
57889649 181974 0 None None None Human 8.2 pIC50 = 8.2 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 486 6 3 4 3.9 CC(C)[C@@H](NC(=O)c1cccc(C(=O)O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398733 181974 0 None None None Human 8.2 pIC50 = 8.2 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 486 6 3 4 3.9 CC(C)[C@@H](NC(=O)c1cccc(C(=O)O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
69435853 214048 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 444 5 2 6 2.9 O=C1COc2cccc(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)c2N1 10.1016/j.bmcl.2013.11.062
CHEMBL3099951 214048 0 None None None Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 444 5 2 6 2.9 O=C1COc2cccc(OC[C@@H](O)CN3CCC4(CC3)Cc3cc(Cl)ccc3O4)c2N1 10.1016/j.bmcl.2013.11.062
73350585 181962 0 None None None Human 8.1 pIC50 = 8.1 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 441 5 2 4 3.4 CC(C)[C@@H](NC(=O)c1cccnc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C2(CC2)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398718 181962 0 None None None Human 8.1 pIC50 = 8.1 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 441 5 2 4 3.4 CC(C)[C@@H](NC(=O)c1cccnc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C2(CC2)C1 10.1016/j.bmcl.2013.04.079
44537841 1390 22 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC1-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of HCC1-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889291 181977 0 None None None Human 8.1 pIC50 = 8.1 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 443 5 2 4 3.6 CC(C)[C@@H](NC(=O)c1ccncc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398736 181977 0 None None None Human 8.1 pIC50 = 8.1 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 443 5 2 4 3.6 CC(C)[C@@H](NC(=O)c1ccncc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
10368788 181594 0 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 502 6 3 7 2.5 O=C(c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CC[C@@H](O)C1 10.1016/j.bmcl.2013.04.047
CHEMBL2391796 181594 0 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 502 6 3 7 2.5 O=C(c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2)N1CC[C@@H](O)C1 10.1016/j.bmcl.2013.04.047
11764610 181604 0 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 516 7 2 7 3.1 CO[C@H]1CCN(C(=O)c2ccc(O)cc2OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)C1 10.1016/j.bmcl.2013.04.047
CHEMBL2391806 181604 0 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 516 7 2 7 3.1 CO[C@H]1CCN(C(=O)c2ccc(O)cc2OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)C1 10.1016/j.bmcl.2013.04.047
57889883 164220 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 444 7 1 2 5.0 CC(C)[C@@H](NC(=O)CCc1ccc(F)cc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180193 164220 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 444 7 1 2 5.0 CC(C)[C@@H](NC(=O)CCc1ccc(F)cc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
24758047 164257 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 390 5 1 2 4.4 CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180501 164257 0 None None None Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 390 5 1 2 4.4 CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
25233580 372935 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 389 4 1 2 4.1 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(F)cc1 10.1021/jm801416q
CHEMBL516495 372935 0 None None None Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 389 4 1 2 4.1 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(F)cc1 10.1021/jm801416q
44453502 311135 0 None None None Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3cccc(Cl)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL402110 311135 0 None None None Human 5.2 pIC50 = 5.2 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 468 4 1 4 4.1 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3cccc(Cl)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
10391877 181628 0 None None None Human 7.2 pIC50 = 7.2 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 517 9 4 7 2.1 CC(=O)NCCNC(=O)c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
CHEMBL2391935 181628 0 None None None Human 7.2 pIC50 = 7.2 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 517 9 4 7 2.1 CC(=O)NCCNC(=O)c1ccc(O)cc1OC[C@@H](O)CN1CCC2(CC1)Cc1cc(Cl)ccc1O2 10.1016/j.bmcl.2013.04.047
11734303 333247 0 None None None Human 7.2 pIC50 = 7.2 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 547 9 3 3 6.5 CC(C)(C)NC(=O)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
CHEMBL435812 333247 0 None None None Human 7.2 pIC50 = 7.2 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 547 9 3 3 6.5 CC(C)(C)NC(=O)NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
10580015 25457 0 None None None Mouse 6.2 pIC50 = 6.2 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 515 4 1 2 7.3 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
CHEMBL1178597 25457 0 None None None Mouse 6.2 pIC50 = 6.2 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 515 4 1 2 7.3 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
10000888 157636 1 None None None Human 5.2 pIC50 = 5.2 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 397 6 1 5 4.2 O=C(CSc1nc2ccccc2s1)NC1CCN(Cc2ccccc2)CC1 10.1016/s0960-894x(01)00176-7
CHEMBL20539 157636 1 None None None Human 5.2 pIC50 = 5.2 Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cellsConcentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
ChEMBL 397 6 1 5 4.2 O=C(CSc1nc2ccccc2s1)NC1CCN(Cc2ccccc2)CC1 10.1016/s0960-894x(01)00176-7
44430732 178811 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 514 9 2 7 3.4 CCNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL234073 178811 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 514 9 2 7 3.4 CCNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
25233581 350933 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 396 4 1 3 3.9 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C#N)cc1 10.1021/jm801416q
CHEMBL462441 350933 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cellsDisplacement of [125I]MIP-1-alpha from human recombinant CCR1 expressed in HEK293 cells
ChEMBL 396 4 1 3 3.9 CN(Cc1ccc(Cl)cc1)C(=O)[C@H]1CCCN1C(=O)Nc1ccc(C#N)cc1 10.1021/jm801416q
57840522 177754 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 504 4 0 5 4.6 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C(F)(F)F)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322864 177754 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 504 4 0 5 4.6 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C(F)(F)F)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
6918497 232475 1 None None None Mouse 6.1 pIC50 = 6.1 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
CHEMBL331897 232475 1 None None None Mouse 6.1 pIC50 = 6.1 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to mouse CCR1 receptors.
ChEMBL 527 5 1 2 7.6 CC[N+]1(C/C2=C/CCCCCC2)CCC(NC(=O)C2c3cc(Cl)ccc3Oc3ccc(Cl)cc32)CC1 10.1021/jm0004244
12425 11 80 None None None Human 4.1 pIC50 = 4.1 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
1318 11 80 None None None Human 4.1 pIC50 = 4.1 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
CHEMBL415879 11 80 None None None Human 4.1 pIC50 = 4.1 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
DB02365 11 80 None None None Human 4.1 pIC50 = 4.1 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
44309364 468890 0 None None None Human 7.1 pIC50 = 7.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 494 12 3 5 4.0 CCNC(=O)C(CCC(C)(C)F)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.022
CHEMBL69123 468890 0 None None None Human 7.1 pIC50 = 7.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 494 12 3 5 4.0 CCNC(=O)C(CCC(C)(C)F)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1 10.1016/j.bmcl.2004.02.022
44430759 178023 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 496 7 2 6 3.6 CNc1c(Nc2cc(Cl)ccc2/C=C/C(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232655 178023 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 496 7 2 6 3.6 CNc1c(Nc2cc(Cl)ccc2/C=C/C(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
10623381 40784 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 448 8 2 3 5.3 NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
CHEMBL125111 40784 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 448 8 2 3 5.3 NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm0201767
25174463 258177 0 None None None Human 6.1 pIC50 = 6.1 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 422 4 3 4 2.5 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)CO)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679647 258177 0 None None None Human 6.1 pIC50 = 6.1 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 422 4 3 4 2.5 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)CO)CC[C@]1(O)c1ccc(Cl)cc1 nan
21070984 177767 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 478 5 0 5 4.7 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(Cl)c(OC(C)C)c2)CC1 10.1016/j.bmcl.2013.01.005
CHEMBL2322877 177767 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 478 5 0 5 4.7 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(Cl)c(OC(C)C)c2)CC1 10.1016/j.bmcl.2013.01.005
24758044 164277 0 None None None Human 7.1 pIC50 = 7.1 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
57888953 164277 0 None None None Human 7.1 pIC50 = 7.1 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
71455572 164277 0 None None None Human 7.1 pIC50 = 7.1 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2180523 164277 0 None None None Human 7.1 pIC50 = 7.1 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2180528 164277 0 None None None Human 7.1 pIC50 = 7.1 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2180534 164277 0 None None None Human 7.1 pIC50 = 7.1 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 398 5 1 2 4.5 CC(C)[C@H](NC(=O)c1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
44430715 291267 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 516 8 2 7 3.5 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(Cl)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL390706 291267 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 516 8 2 7 3.5 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(Cl)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453402 195937 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cc(Cl)cc(Cl)c1 10.1016/j.bmcl.2007.09.068
CHEMBL257698 195937 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cc(Cl)cc(Cl)c1 10.1016/j.bmcl.2007.09.068
11072063 40489 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 597 11 3 4 7.2 COc1ccc(NC(=O)NCC(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)(c2ccccc2)c2ccccc2)cc1 10.1021/jm0201767
CHEMBL124084 40489 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 597 11 3 4 7.2 COc1ccc(NC(=O)NCC(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)(c2ccccc2)c2ccccc2)cc1 10.1021/jm0201767
59444266 348743 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 477 5 2 4 4.4 CC(C)(CC(=O)N1CCC(O)(c2ncc(Cl)cc2Cl)C(C)(C)C1)NC(=O)c1ccccc1 nan
CHEMBL4559773 348743 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 477 5 2 4 4.4 CC(C)(CC(=O)N1CCC(O)(c2ncc(Cl)cc2Cl)C(C)(C)C1)NC(=O)c1ccccc1 nan
68818964 214055 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 427 5 2 6 2.3 N[C@H](COc1cccc2c1NC(=O)CO2)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2013.11.062
CHEMBL3099958 214055 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysisDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cell membranes after 1.5 hrs by microbeta counting analysis
ChEMBL 427 5 2 6 2.3 N[C@H](COc1cccc2c1NC(=O)CO2)CN1CCC2(CC1)Cc1cc(F)ccc1O2 10.1016/j.bmcl.2013.11.062
12425 11 80 None None None Human 4.1 pIC50 = 4.1 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
1318 11 80 None None None Human 4.1 pIC50 = 4.1 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
CHEMBL415879 11 80 None None None Human 4.1 pIC50 = 4.1 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
DB02365 11 80 None None None Human 4.1 pIC50 = 4.1 Binding
Displacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrsDisplacement of [125I]-CCL3 from human CCR1 transfected in COS7 cells coexpressing chimeric Gqi4myr after 3 hrs
ChEMBL 180 0 0 2 2.8 C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1 10.1021/jm301121j
12112109 291923 0 None None None Human 8.1 pIC50 = 8.1 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 491 8 3 5 3.1 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2NC(=O)NCCN)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
CHEMBL391238 291923 0 None None None Human 8.1 pIC50 = 8.1 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 491 8 3 5 3.1 C[C@H]1CN(C(=O)COc2ccc(Cl)cc2NC(=O)NCCN)[C@H](C)CN1Cc1ccc(F)cc1 10.1016/j.bmcl.2007.03.037
57840435 177732 0 None None None Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 424 5 0 5 4.0 COc1cc(N2CCN(C(=O)Cn3nc(C(C)C)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322844 177732 0 None None None Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 424 5 0 5 4.0 COc1cc(N2CCN(C(=O)Cn3nc(C(C)C)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
58778003 177748 0 None None None Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 494 4 0 5 4.0 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Br)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322859 177748 0 None None None Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 494 4 0 5 4.0 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Br)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
24758295 164261 0 None None None Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 418 6 1 2 5.2 CC(C)[C@@H](NC(=O)CC1CCCCC1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180505 164261 0 None None None Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 418 6 1 2 5.2 CC(C)[C@@H](NC(=O)CC1CCCCC1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44309312 468765 0 None None None Human 8.1 pIC50 = 8.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 460 9 3 5 3.4 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCCC1 10.1016/j.bmcl.2004.02.021
44309312 468765 0 None None None Human 8.1 pIC50 = 8.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 460 9 3 5 3.4 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCCC1 10.1016/j.bmcl.2004.02.022
44309337 468765 0 None None None Human 8.1 pIC50 = 8.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 460 9 3 5 3.4 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCCC1 10.1016/j.bmcl.2004.02.021
44309337 468765 0 None None None Human 8.1 pIC50 = 8.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 460 9 3 5 3.4 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCCC1 10.1016/j.bmcl.2004.02.022
CHEMBL68145 468765 0 None None None Human 8.1 pIC50 = 8.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 460 9 3 5 3.4 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCCC1 10.1016/j.bmcl.2004.02.021
CHEMBL68145 468765 0 None None None Human 8.1 pIC50 = 8.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 460 9 3 5 3.4 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCCC1 10.1016/j.bmcl.2004.02.022
CHEMBL69375 468765 0 None None None Human 8.1 pIC50 = 8.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 460 9 3 5 3.4 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCCC1 10.1016/j.bmcl.2004.02.021
CHEMBL69375 468765 0 None None None Human 8.1 pIC50 = 8.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 460 9 3 5 3.4 NC(=O)C(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C1CCCCC1 10.1016/j.bmcl.2004.02.022
71680936 181991 0 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 563 8 3 6 3.2 CC(C)[C@@H](NC(=O)C1CCCC1(O)CCN1CCOCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398750 181991 0 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 563 8 3 6 3.2 CC(C)[C@@H](NC(=O)C1CCCC1(O)CCN1CCOCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
10254761 181596 0 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 484 6 2 6 2.6 Cc1ccc(C(=O)N2CC[C@H](O)C2)c(OC[C@@H](O)CN2CCC3(CC2)Cc2cc(F)ccc2O3)c1 10.1016/j.bmcl.2013.04.047
CHEMBL2391798 181596 0 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 484 6 2 6 2.6 Cc1ccc(C(=O)N2CC[C@H](O)C2)c(OC[C@@H](O)CN2CCC3(CC2)Cc2cc(F)ccc2O3)c1 10.1016/j.bmcl.2013.04.047
57889649 181974 0 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 486 6 3 4 3.9 CC(C)[C@@H](NC(=O)c1cccc(C(=O)O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398733 181974 0 None None None Human 8.1 pIC50 = 8.1 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 486 6 3 4 3.9 CC(C)[C@@H](NC(=O)c1cccc(C(=O)O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
24759420 164269 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 448 5 1 2 5.7 CC(C)C(NC(=O)c1ccc2ccccc2c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180513 164269 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 448 5 1 2 5.7 CC(C)C(NC(=O)c1ccc2ccccc2c1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44453403 195510 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1c(Cl)cccc1Cl 10.1016/j.bmcl.2007.09.068
CHEMBL255629 195510 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.3 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1c(Cl)cccc1Cl 10.1016/j.bmcl.2007.09.068
44430736 309585 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 576 10 2 7 4.5 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2ccccc2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL397956 309585 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 576 10 2 7 4.5 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCc2ccccc2)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453263 311580 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 442 7 2 4 3.6 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL404732 311580 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 442 7 2 4 3.6 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)cc1 10.1016/j.bmcl.2007.09.068
10695296 200030 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 460 4 1 3 6.6 O=C(NC1CCN(CC2CCCCCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1016/j.ejmech.2020.113085
CHEMBL285703 200030 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assayInhibition of human CCR1 transfected in CHO cells incubated for 1 hr in presence of 125I-chemokine by radioactivity based assay
ChEMBL 460 4 1 3 6.6 O=C(NC1CCN(CC2CCCCCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1016/j.ejmech.2020.113085
10816699 25456 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 433 6 1 1 5.9 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C(c2ccccc2)c2ccccc2)CC1 10.1021/jm0004244
CHEMBL1178593 25456 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 433 6 1 1 5.9 C[N+]1(CC2CCCCCCC2)CCC(NC(=O)C(c2ccccc2)c2ccccc2)CC1 10.1021/jm0004244
10695296 200030 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 460 4 1 3 6.6 O=C(NC1CCN(CC2CCCCCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
CHEMBL285703 200030 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 460 4 1 3 6.6 O=C(NC1CCN(CC2CCCCCCCCC2)CC1)C1c2ccccc2Oc2ccccc21 10.1021/jm0004244
44309091 468731 0 None None None Human 5.1 pIC50 = 5.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 439 10 3 4 4.2 CC(C)C[C@H](C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1)C(N)=O 10.1016/j.bmcl.2004.02.020
CHEMBL67809 468731 0 None None None Human 5.1 pIC50 = 5.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 439 10 3 4 4.2 CC(C)C[C@H](C[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1)C(N)=O 10.1016/j.bmcl.2004.02.020
59444207 336368 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 470 7 2 3 4.4 CC(C)[C@@H](CNC(=O)Cc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
CHEMBL4468705 336368 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 470 7 2 3 4.4 CC(C)[C@@H](CNC(=O)Cc1ccccc1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
49865901 40076 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 463 4 1 4 5.7 Cc1nc([C@H]2CCCN2C(=O)Nc2ccc(C(F)(F)F)cc2)n(Cc2ccc(Cl)cc2)n1 10.1016/j.bmcl.2010.07.082
CHEMBL1224121 40076 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPADisplacement of [125I]-MIP1-alpha from human recombinant CCR1 expressed in HEK293 cells after 4 hrs by SPA
ChEMBL 463 4 1 4 5.7 Cc1nc([C@H]2CCCN2C(=O)Nc2ccc(C(F)(F)F)cc2)n(Cc2ccc(Cl)cc2)n1 10.1016/j.bmcl.2010.07.082
59474969 258187 0 None None None Human 6.1 pIC50 = 6.1 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 482 4 2 3 5.2 CC1(C)CN(C(=O)[C@H]2CCCC[C@@]2(C)NC(=O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679658 258187 0 None None None Human 6.1 pIC50 = 6.1 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 482 4 2 3 5.2 CC1(C)CN(C(=O)[C@H]2CCCC[C@@]2(C)NC(=O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
24758745 164254 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 7 1 2 4.6 CC[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180498 164254 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 7 1 2 4.6 CC[C@@H](NC(=O)CCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44309245 468458 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 556 13 3 5 5.2 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)NCc1ccccc1 10.1016/j.bmcl.2004.02.022
CHEMBL65784 468458 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 556 13 3 5 5.2 CC(C)(F)CCC(C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(=O)NCc1ccccc1 10.1016/j.bmcl.2004.02.022
57888886 164282 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 444 6 2 4 4.1 CC(C)C(NC(=O)OCc1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180529 164282 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 444 6 2 4 4.1 CC(C)C(NC(=O)OCc1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
25174628 258178 0 None None None Human 6.1 pIC50 = 6.1 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 498 5 3 4 4.2 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)[C@H](O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
25174629 258178 0 None None None Human 6.1 pIC50 = 6.1 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 498 5 3 4 4.2 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)[C@H](O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679648 258178 0 None None None Human 6.1 pIC50 = 6.1 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 498 5 3 4 4.2 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)[C@H](O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679649 258178 0 None None None Human 6.1 pIC50 = 6.1 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 498 5 3 4 4.2 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)[C@H](O)c2ccccc2)CC[C@]1(O)c1ccc(Cl)cc1 nan
9999626 178927 0 None None None Human 6.1 pIC50 = 6.1 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 376 5 0 3 3.6 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1 10.1016/j.bmcl.2007.03.037
CHEMBL234622 178927 0 None None None Human 6.1 pIC50 = 6.1 Binding
Binding Affinity at CCL3Binding Affinity at CCL3
ChEMBL 376 5 0 3 3.6 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1 10.1016/j.bmcl.2007.03.037
57889944 164294 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 6 1 2 5.2 Cc1ccccc1C(=O)NC(CC(C)C)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180543 164294 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 426 6 1 2 5.2 Cc1ccccc1C(=O)NC(CC(C)C)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
68963698 181605 0 None None None Human 7.1 pIC50 = 7.1 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 543 7 3 7 2.6 CC(=O)N[C@H]1CCN(C(=O)c2ccc(O)cc2OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)C1 10.1016/j.bmcl.2013.04.047
CHEMBL2391807 181605 0 None None None Human 7.1 pIC50 = 7.1 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assayAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of MIP-1alpha-induced chemotaxis after 2 hrs by fluorescence assay
ChEMBL 543 7 3 7 2.6 CC(=O)N[C@H]1CCN(C(=O)c2ccc(O)cc2OC[C@@H](O)CN2CCC3(CC2)Cc2cc(Cl)ccc2O3)C1 10.1016/j.bmcl.2013.04.047
44453467 196094 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 502 4 1 4 4.8 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)c(Cl)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL258359 196094 0 None None None Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 502 4 1 4 4.8 O=S(=O)(c1ccccc1Cl)N1CCC(N2CCC(O)(c3ccc(Cl)c(Cl)c3)CC2)CC1 10.1016/j.bmcl.2007.09.068
10985078 233741 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 635 10 3 3 8.2 O=C(NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1)Nc1ccc(C(F)(F)F)cc1 10.1021/jm0201767
CHEMBL333865 233741 0 None None None Human 6.1 pIC50 = 6.1 Binding
Inhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cellsInhibitory activity against human Chemokine receptor type 1 expressed in chinese hamster ovary cells
ChEMBL 635 10 3 3 8.2 O=C(NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1)Nc1ccc(C(F)(F)F)cc1 10.1021/jm0201767
57889635 233486 0 None None None Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 435 4 2 3 3.6 CC(C)[C@@H](NC(=O)N1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
CHEMBL3334819 233486 0 None None None Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 435 4 2 3 3.6 CC(C)[C@@H](NC(=O)N1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1021/jm5003167
68818375 178229 0 None None None Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 443 7 2 6 3.0 COc1ccc(NC(C)=O)c(OC[C@@H](N)CN2CCC3(CC2)Cc2cc(F)ccc2O3)c1 10.1016/j.bmcl.2012.12.095
CHEMBL2332938 178229 0 None None None Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrsDisplacement of [125I]MIP-1alpha from human recombinant CCR1 expressed in HEK293 cells after 1.5 hrs
ChEMBL 443 7 2 6 3.0 COc1ccc(NC(C)=O)c(OC[C@@H](N)CN2CCC3(CC2)Cc2cc(F)ccc2O3)c1 10.1016/j.bmcl.2012.12.095
44309397 468791 0 None None None Human 8.1 pIC50 = 8.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 466 11 3 5 3.4 CC(C)(F)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
CHEMBL68366 468791 0 None None None Human 8.1 pIC50 = 8.1 Binding
Inhibition of CCL3 binding to C-C chemokine receptor type 1Inhibition of CCL3 binding to C-C chemokine receptor type 1
ChEMBL 466 11 3 5 3.4 CC(C)(F)CC[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)C(N)=O 10.1016/j.bmcl.2004.02.022
52916803 335526 28 None None None Human 8.1 pIC50 = 8.1 Binding
Receptor internalizationReceptor internalization
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL4507278
CHEMBL4456123 335526 28 None None None Human 8.1 pIC50 = 8.1 Binding
Receptor internalizationReceptor internalization
ChEMBL 451 5 1 7 2.8 CS(=O)(=O)c1cc(C2(NC(=O)c3cncc4c3cnn4-c3ccc(F)cc3)CC2)ccn1 10.6019/CHEMBL4507278
44537841 1390 22 None None None Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MCP3-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MCP3-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57889181 1390 22 None None None Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MCP3-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MCP3-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
9497 1390 22 None None None Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MCP3-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MCP3-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL2398716 1390 22 None None None Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MCP3-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MCP3-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
CHEMBL3334824 1390 22 None None None Human 8.0 pIC50 = 8.0 Binding
Antagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MCP3-induced chemotaxis after 60 minsAntagonist activity at CCR1 receptor in human THP1 cells assessed as inhibition of MCP3-induced chemotaxis after 60 mins
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 10.1021/jm5003167
57888707 182006 0 None None None Human 8.0 pIC50 = 8.0 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 413 6 1 3 3.8 CC(C)[C@@H](NC(=O)Cc1ccncc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
CHEMBL2398768 182006 0 None None None Human 8.0 pIC50 = 8.0 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 413 6 1 3 3.8 CC(C)[C@@H](NC(=O)Cc1ccncc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.04.079
10555551 25450 0 None None None Human 8.0 pIC50 = 8.0 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 473 6 1 2 6.6 C=CC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
CHEMBL1178575 25450 0 None None None Human 8.0 pIC50 = 8.0 Binding
Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.Inhibitory activity against [125I]-MIP-1 alpha binding to human CCR1 receptors.
ChEMBL 473 6 1 2 6.6 C=CC[N+]1(CC2CCCCCCC2)CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1 10.1021/jm0004244
57888900 182005 0 None None None Human 8.0 pIC50 = 8 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 521 6 3 5 2.9 CC(C)[C@@H](NC(=O)c1cccc(S(N)(=O)=O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398767 182005 0 None None None Human 8.0 pIC50 = 8 Binding
Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxisAntagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis
ChEMBL 521 6 3 5 2.9 CC(C)[C@@H](NC(=O)c1cccc(S(N)(=O)=O)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
57888966 182009 0 None None None Human 8.0 pIC50 = 8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1cccc(Cl)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
CHEMBL2398771 182009 0 None None None Human 8.0 pIC50 = 8 Binding
Binding affinity to human CCR1Binding affinity to human CCR1
ChEMBL 476 5 2 3 4.9 CC(C)[C@@H](NC(=O)c1cccc(Cl)c1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 10.1016/j.bmcl.2013.04.079
44430725 332532 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 480 8 2 7 2.6 CNc1c(Nc2cc(C)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL430356 332532 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 480 8 2 7 2.6 CNc1c(Nc2cc(C)ccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
25022507 311387 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Br)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL403728 311387 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 512 4 1 4 4.2 O=S(=O)(c1ccccc1Br)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
44453361 332112 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 456 7 2 4 4.0 Cc1cccc(Cl)c1S(=O)(=O)NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL429419 332112 0 None None None Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 456 7 2 4 4.0 Cc1cccc(Cl)c1S(=O)(=O)NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2007.09.068
21070989 177765 0 None None None Mouse 6.1 pIC50 = 6.1 Binding
Antagonist activity at CCR1 in mouse WEHI274.1 cells assessed as inhibition of CCL3/MIP-1alpha-induced chemotaxisAntagonist activity at CCR1 in mouse WEHI274.1 cells assessed as inhibition of CCL3/MIP-1alpha-induced chemotaxis
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322875 177765 0 None None None Mouse 6.1 pIC50 = 6.1 Binding
Antagonist activity at CCR1 in mouse WEHI274.1 cells assessed as inhibition of CCL3/MIP-1alpha-induced chemotaxisAntagonist activity at CCR1 in mouse WEHI274.1 cells assessed as inhibition of CCL3/MIP-1alpha-induced chemotaxis
ChEMBL 450 4 0 5 3.9 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
44453165 196097 0 None None None Human 5.1 pIC50 = 5.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 492 8 2 5 3.9 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(OC(F)(F)F)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL258362 196097 0 None None None Human 5.1 pIC50 = 5.1 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 492 8 2 5 3.9 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(OC(F)(F)F)cc1 10.1016/j.bmcl.2007.09.068
44453229 195770 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 426 7 2 4 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(F)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL256889 195770 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 426 7 2 4 3.1 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(F)cc1 10.1016/j.bmcl.2007.09.068
57840460 177744 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 4 0 5 4.3 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)C[C@H]2C)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322855 177744 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 464 4 0 5 4.3 COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)C[C@H]2C)ccc1Cl 10.1016/j.bmcl.2013.01.005
44430722 177716 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 466 8 2 7 2.3 CNc1c(Nc2ccccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232252 177716 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 466 8 2 7 2.3 CNc1c(Nc2ccccc2OCC(=O)N2CCN(Cc3ccc(F)cc3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
1370410 177778 10 None None None Human 7.0 pIC50 = 7.0 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced chemotaxisAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced chemotaxis
ChEMBL 404 3 0 4 3.4 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(F)cc2)CC1 10.1016/j.bmcl.2013.01.005
CHEMBL2322888 177778 10 None None None Human 7.0 pIC50 = 7.0 Binding
Antagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced chemotaxisAntagonist activity at CCR1 in human THP1 cells assessed as inhibition of CCL3/MIP-1alpha-induced chemotaxis
ChEMBL 404 3 0 4 3.4 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(F)cc2)CC1 10.1016/j.bmcl.2013.01.005
25174306 258175 0 None None None Human 6.0 pIC50 = 6.0 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 503 6 2 4 4.3 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)CCN2CCCCC2)CC[C@]1(O)c1ccc(Cl)cc1 nan
CHEMBL3679645 258175 0 None None None Human 6.0 pIC50 = 6.0 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 503 6 2 4 4.3 CC1(C)CN(C(=O)[C@H]2CCCC[C@H]2NC(=O)CCN2CCCCC2)CC[C@]1(O)c1ccc(Cl)cc1 nan
57889234 164283 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 2 3 3.1 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(F)cc2)CC1 10.1021/jm300896d
CHEMBL2180530 164283 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 398 5 2 3 3.1 CC(C)C(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(F)cc2)CC1 10.1021/jm300896d
44453167 196098 0 None None None Human 5.0 pIC50 = 5.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.0 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(C(F)(F)F)cc1 10.1016/j.bmcl.2007.09.068
CHEMBL258363 196098 0 None None None Human 5.0 pIC50 = 5.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 476 7 2 4 4.0 O=S(=O)(NCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(C(F)(F)F)cc1 10.1016/j.bmcl.2007.09.068
57991690 164270 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 440 8 1 2 5.2 CC(C)[C@@H](NC(=O)CCCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
CHEMBL2180516 164270 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 440 8 1 2 5.2 CC(C)[C@@H](NC(=O)CCCc1ccccc1)C(=O)N1CCC(c2ccc(Cl)cc2)CC1 10.1021/jm300896d
44430746 177992 0 None None None Mouse 6.0 pIC50 = 6.0 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 530 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCO)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232638 177992 0 None None None Mouse 6.0 pIC50 = 6.0 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 530 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCO)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44430748 178095 0 None None None Mouse 6.0 pIC50 = 6.0 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 529 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232837 178095 0 None None None Mouse 6.0 pIC50 = 6.0 Binding
Binding affinity at mouse CCR1Binding affinity at mouse CCR1
ChEMBL 529 10 3 8 2.3 C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1Nc1c(NCCN)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
57840315 177737 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 5 1 6 2.3 COc1cc(N2CCN(C(=O)Cn3nc(CO)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
CHEMBL2322849 177737 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 412 5 1 6 2.3 COc1cc(N2CCN(C(=O)Cn3nc(CO)c(Cl)c3C)CC2)ccc1Cl 10.1016/j.bmcl.2013.01.005
44430717 177636 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 518 8 2 7 3.1 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)c(F)c3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
CHEMBL232043 177636 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 expressed in THP1 cells
ChEMBL 518 8 2 7 3.1 CNc1c(Nc2cc(Cl)ccc2OCC(=O)N2CCN(Cc3ccc(F)c(F)c3)C[C@H]2C)c(=O)c1=O 10.1016/j.bmcl.2007.03.104
44453225 196100 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 440 4 1 5 3.5 O=S(=O)(c1cccs1)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
CHEMBL258368 196100 0 None None None Human 6.0 pIC50 = 6.0 Binding
Displacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cellsDisplacement of [125I]MIP1-alpha from human CCR1 receptor expressed in THP1 cells
ChEMBL 440 4 1 5 3.5 O=S(=O)(c1cccs1)N1CCC(N2CCC(O)(c3ccc(Cl)cc3)CC2)CC1 10.1016/j.bmcl.2007.09.068
21071094 177780 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 420 3 0 4 3.9 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.01.005
CHEMBL2322890 177780 0 None None None Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 420 3 0 4 3.9 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(Cl)cc2)CC1 10.1016/j.bmcl.2013.01.005
21071099 177824 0 None None None Human 5.0 pIC50 = 5.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 454 3 0 4 4.2 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(C(F)(F)F)cc2)CC1 10.1016/j.bmcl.2013.01.005
CHEMBL2323419 177824 0 None None None Human 5.0 pIC50 = 5.0 Binding
Displacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cellsDisplacement of [125I]-CCL3/MIP-1alpha from CCR1 in human THP1 cells
ChEMBL 454 3 0 4 4.2 Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCN(c2ccc(C(F)(F)F)cc2)CC1 10.1016/j.bmcl.2013.01.005
59444200 347298 0 None None None Human 6.0 pIC50 = 6 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 514 7 2 5 4.6 CCOC(=O)c1cc(C2(O)CCN(C(=O)CC(C)(C)NC(=O)c3ccccc3)CC2(C)C)ccc1Cl nan
CHEMBL4522473 347298 0 None None None Human 6.0 pIC50 = 6 Binding
Displacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assayDisplacement of [125I]-MIP-1alpha from CCR1 in human THP-1 cells after 12 h by scintillation proximity assay
ChEMBL 514 7 2 5 4.6 CCOC(=O)c1cc(C2(O)CCN(C(=O)CC(C)(C)NC(=O)c3ccccc3)CC2(C)C)ccc1Cl nan
25176401 258173 0 None None None Human 6.0 pIC50 = 6 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 422 3 2 4 3.7 COC(=O)N[C@@H]1CCCC[C@@H]1C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
CHEMBL3679643 258173 0 None None None Human 6.0 pIC50 = 6 Binding
Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).Scintillation Proximity Assay (SPA): CCR1 ligand binding using scintillation proximity assay (SPA).
ChEMBL 422 3 2 4 3.7 COC(=O)N[C@@H]1CCCC[C@@H]1C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
512282 1562 44 None 199 2 Human 9.0 pKd = 9 Binding
Binding affinity to human CCR1 by radioligand binding assayBinding affinity to human CCR1 by radioligand binding assay
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm300682j
767 1562 44 None 199 2 Human 9.0 pKd = 9 Binding
Binding affinity to human CCR1 by radioligand binding assayBinding affinity to human CCR1 by radioligand binding assay
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm300682j
CHEMBL232656 1562 44 None 199 2 Human 9.0 pKd = 9 Binding
Binding affinity to human CCR1 by radioligand binding assayBinding affinity to human CCR1 by radioligand binding assay
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm300682j
512282 1562 44 None -199 2 Mouse 6.7 pKd = 6.7 Binding
Binding affinity to mouse CCR1 by radioligand binding assayBinding affinity to mouse CCR1 by radioligand binding assay
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm300682j
767 1562 44 None -199 2 Mouse 6.7 pKd = 6.7 Binding
Binding affinity to mouse CCR1 by radioligand binding assayBinding affinity to mouse CCR1 by radioligand binding assay
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm300682j
CHEMBL232656 1562 44 None -199 2 Mouse 6.7 pKd = 6.7 Binding
Binding affinity to mouse CCR1 by radioligand binding assayBinding affinity to mouse CCR1 by radioligand binding assay
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm300682j
25109291 366002 9 None 56 12 Human 10.4 pKi = 10.4 Binding
Displacement of radiolabeled MIP1alpha from human CCR1 receptorDisplacement of radiolabeled MIP1alpha from human CCR1 receptor
ChEMBL 327 1 2 6 1.7 Nc1nc2c(c(N3CCNCC3)n1)CCC1=C2[C@@H]2CCCC[C@@H]2O1 10.1021/jm8007618
CHEMBL519240 366002 9 None 56 12 Human 10.4 pKi = 10.4 Binding
Displacement of radiolabeled MIP1alpha from human CCR1 receptorDisplacement of radiolabeled MIP1alpha from human CCR1 receptor
ChEMBL 327 1 2 6 1.7 Nc1nc2c(c(N3CCNCC3)n1)CCC1=C2[C@@H]2CCCC[C@@H]2O1 10.1021/jm8007618
57889392 255028 0 None None None Human 9.3 pKi = 9.3 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 423 5 3 3 3.5 CC(C)NC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C nan
CHEMBL3656279 255028 0 None None None Human 9.3 pKi = 9.3 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 423 5 3 3 3.5 CC(C)NC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C nan
57889423 181988 0 None None None Human 9.2 pKi = 9.2 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 434 5 2 3 4.1 CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
CHEMBL2398747 181988 0 None None None Human 9.2 pKi = 9.2 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 434 5 2 3 4.1 CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1 nan
512282 1562 44 None None None Human 9.0 pKi = 9 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm300682j
767 1562 44 None None None Human 9.0 pKi = 9 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm300682j
CHEMBL232656 1562 44 None None None Human 9.0 pKi = 9 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10.1021/jm300682j
10371087 155195 0 None None None Human 8.7 pKi = 8.7 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 584 6 2 5 6.0 NCC1CCCN(C(=O)c2ccc3c(c2)C(C(=O)NC2CCN(C/C4=C/CCCCCCC4)CC2)c2ccccc2O3)C1 10.1021/jm300682j
CHEMBL2178571 155195 0 None None None Human 8.7 pKi = 8.7 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 584 6 2 5 6.0 NCC1CCCN(C(=O)c2ccc3c(c2)C(C(=O)NC2CCN(C/C4=C/CCCCCCC4)CC2)c2ccccc2O3)C1 10.1021/jm300682j
10111333 349467 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 395 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4577133 349467 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 395 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
71461438 174964 0 None -100 3 Human 6.0 pKi = 6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 416 5 1 5 4.1 O=S(=O)(Nc1cc(Cl)ccc1Cn1cnnc1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207082 174964 0 None -100 3 Human 6.0 pKi = 6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 416 5 1 5 4.1 O=S(=O)(Nc1cc(Cl)ccc1Cn1cnnc1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
71214725 174965 0 None -25 3 Human 6.0 pKi = 6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 416 5 1 5 4.1 O=S(=O)(Nc1cc(Cl)ccc1Cn1cncn1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207083 174965 0 None -25 3 Human 6.0 pKi = 6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 416 5 1 5 4.1 O=S(=O)(Nc1cc(Cl)ccc1Cn1cncn1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
71461439 174969 0 None -10 3 Human 6.0 pKi = 6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 382 5 1 5 3.4 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1ccc(Cl)cc1 10.1016/j.bmcl.2012.09.020
CHEMBL2207087 174969 0 None -10 3 Human 6.0 pKi = 6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 382 5 1 5 3.4 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1ccc(Cl)cc1 10.1016/j.bmcl.2012.09.020
71452488 174975 0 None -19 3 Human 6.0 pKi = 6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 388 5 1 6 3.5 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1ccc(Cl)s1 10.1016/j.bmcl.2012.09.020
CHEMBL2207093 174975 0 None -19 3 Human 6.0 pKi = 6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 388 5 1 6 3.5 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1ccc(Cl)s1 10.1016/j.bmcl.2012.09.020
71461440 174979 0 None -31 3 Human 6.0 pKi = 6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 400 5 1 5 3.6 O=S(=O)(Nc1cc(F)ccc1Cn1ccnn1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207097 174979 0 None -31 3 Human 6.0 pKi = 6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 400 5 1 5 3.6 O=S(=O)(Nc1cc(F)ccc1Cn1ccnn1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
15604497 174981 0 None -39 3 Human 6.0 pKi = 6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 432 5 1 7 3.0 Cn1nnnc1Cc1ncc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207099 174981 0 None -39 3 Human 6.0 pKi = 6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 432 5 1 7 3.0 Cn1nnnc1Cc1ncc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
10809142 78844 0 None None None Human 6.0 pKi = 6 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 369 6 1 4 4.1 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccnc1 10.1021/jm990316l
CHEMBL143741 78844 0 None None None Human 6.0 pKi = 6 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 369 6 1 4 4.1 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccnc1 10.1021/jm990316l
68557448 334779 0 None None None Human 6.0 pKi = 6.0 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 417 5 1 5 4.2 COc1cccc(N2CCC(C(O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)c1 nan
CHEMBL4445508 334779 0 None None None Human 6.0 pKi = 6.0 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 417 5 1 5 4.2 COc1cccc(N2CCC(C(O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)c1 nan
10788075 238171 0 None None None Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 416 7 1 4 5.3 N#CC(CCCN1CCC(O)(c2cccs2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL344751 238171 0 None None None Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 416 7 1 4 5.3 N#CC(CCCN1CCC(O)(c2cccs2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
10111333 349467 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 395 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4577133 349467 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 395 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
155568814 350038 0 None None None Human 6.9 pKi = 6.9 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 403 5 1 5 3.8 COc1cc(N2CCC(C(O)Cn3ccc(C(F)(F)F)n3)CC2)ccc1Cl nan
CHEMBL4590794 350038 0 None None None Human 6.9 pKi = 6.9 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 403 5 1 5 3.8 COc1cc(N2CCC(C(O)Cn3ccc(C(F)(F)F)n3)CC2)ccc1Cl nan
10599794 77706 0 None None None Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 453 8 1 4 5.3 CN(C)c1ccc(C2(O)CCN(CCCC(C#N)(c3ccccc3)c3ccccc3)CC2)cc1 10.1021/jm990316l
CHEMBL142628 77706 0 None None None Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 453 8 1 4 5.3 CN(C)c1ccc(C2(O)CCN(CCCC(C#N)(c3ccccc3)c3ccccc3)CC2)cc1 10.1021/jm990316l
10526132 144690 0 None None None Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 419 7 1 2 6.2 OC1(c2ccc(Cl)cc2)CCN(CCCC(c2ccccc2)c2ccccc2)CC1 10.1021/jm990316l
CHEMBL198935 144690 0 None None None Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 419 7 1 2 6.2 OC1(c2ccc(Cl)cc2)CCN(CCCC(c2ccccc2)c2ccccc2)CC1 10.1021/jm990316l
44362079 237946 0 None None None Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 422 5 1 3 5.2 N#CC1(CCCN2CCC(O)(c3ccccc3)CC2)c2ccccc2Cc2ccccc21 10.1021/jm990316l
CHEMBL343032 237946 0 None None None Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 422 5 1 3 5.2 N#CC1(CCCN2CCC(O)(c3ccccc3)CC2)c2ccccc2Cc2ccccc21 10.1021/jm990316l
24863547 348754 0 None None None Human 6.9 pKi = 6.9 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 484 5 1 5 5.4 COc1cc(N2CCC(C(N)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)c(Cl)cc1Cl nan
CHEMBL4559982 348754 0 None None None Human 6.9 pKi = 6.9 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 484 5 1 5 5.4 COc1cc(N2CCC(C(N)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)c(Cl)cc1Cl nan
10811393 78377 0 None None None Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 407 7 1 4 4.8 N#CCC(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
CHEMBL143194 78377 0 None None None Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 407 7 1 4 4.8 N#CCC(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
24863719 349849 0 None None None Human 5.9 pKi = 5.9 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 465 5 1 5 5.2 COc1cc(N2CCC(C)(C(O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl nan
CHEMBL4586066 349849 0 None None None Human 5.9 pKi = 5.9 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 465 5 1 5 5.2 COc1cc(N2CCC(C)(C(O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)ccc1Cl nan
71214976 174984 0 None -100 3 Human 5.9 pKi = 5.9 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 450 5 1 5 4.5 O=S(=O)(Nc1cc(Cl)c(Cl)cc1Cn1ccnn1)c1cccc(C(F)(F)F)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207101 174984 0 None -100 3 Human 5.9 pKi = 5.9 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 450 5 1 5 4.5 O=S(=O)(Nc1cc(Cl)c(Cl)cc1Cn1ccnn1)c1cccc(C(F)(F)F)c1 10.1016/j.bmcl.2012.09.020
10547456 238325 0 None None None Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 374 6 1 4 4.8 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccs1 10.1021/jm990316l
CHEMBL346205 238325 0 None None None Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 374 6 1 4 4.8 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccs1 10.1021/jm990316l
10503785 239731 0 None None None Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 451 7 1 4 5.3 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)N1CCCCC1 10.1021/jm990316l
CHEMBL357434 239731 0 None None None Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 451 7 1 4 5.3 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)N1CCCCC1 10.1021/jm990316l
10528677 333206 0 None None None Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 478 7 1 3 6.6 N#CC(CCCN1CCC(O)(c2cc(Cl)cc(Cl)c2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL435480 333206 0 None None None Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 478 7 1 3 6.6 N#CC(CCCN1CCC(O)(c2cc(Cl)cc(Cl)c2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
10812461 160350 0 None None None Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 428 7 1 3 5.4 N#CC(CCCN1CCC(O)(c2ccc(F)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL2112832 160350 0 None None None Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 428 7 1 3 5.4 N#CC(CCCN1CCC(O)(c2ccc(F)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
10133557 337057 0 None -1 2 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 367 3 1 3 4.4 CC(=O)C1=C(O)C(=O)N(c2ccc(C(F)(F)F)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4483771 337057 0 None -1 2 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 367 3 1 3 4.4 CC(=O)C1=C(O)C(=O)N(c2ccc(C(F)(F)F)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
10645391 67200 0 None None None Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 412 8 1 4 5.1 CCOc1ccc(C(C#N)CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1 10.1021/jm990316l
CHEMBL142107 67200 0 None None None Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 412 8 1 4 5.1 CCOc1ccc(C(C#N)CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1 10.1021/jm990316l
10133557 337057 0 None -1 2 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 367 3 1 3 4.4 CC(=O)C1=C(O)C(=O)N(c2ccc(C(F)(F)F)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4483771 337057 0 None -1 2 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 367 3 1 3 4.4 CC(=O)C1=C(O)C(=O)N(c2ccc(C(F)(F)F)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
68552829 335851 0 None None None Human 6.8 pKi = 6.8 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 473 7 2 6 3.2 COc1cc(N2CCC(C(Cn3nc(C(F)(F)F)cc3C)NC(=O)CN)CC2)ccc1Cl nan
CHEMBL4461035 335851 0 None None None Human 6.8 pKi = 6.8 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 473 7 2 6 3.2 COc1cc(N2CCC(C(Cn3nc(C(F)(F)F)cc3C)NC(=O)CN)CC2)ccc1Cl nan
12093167 327835 32 None -1 2 Human 7.8 pKi = 7.8 Binding
Binding affinity to CCR1 (unknown origin) assessed as inhibition constantBinding affinity to CCR1 (unknown origin) assessed as inhibition constant
ChEMBL 351 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.4c02102
CHEMBL4475389 327835 32 None -1 2 Human 7.8 pKi = 7.8 Binding
Binding affinity to CCR1 (unknown origin) assessed as inhibition constantBinding affinity to CCR1 (unknown origin) assessed as inhibition constant
ChEMBL 351 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.4c02102
12093167 327835 32 None -1 2 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 351 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4475389 327835 32 None -1 2 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 351 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
12093167 327835 32 None -1 2 Human 7.8 pKi = 7.8 Binding
Binding affinity to CCR1 (unknown origin) assessed as inhibition constantBinding affinity to CCR1 (unknown origin) assessed as inhibition constant
ChEMBL 351 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.4c02102
CHEMBL4475389 327835 32 None -1 2 Human 7.8 pKi = 7.8 Binding
Binding affinity to CCR1 (unknown origin) assessed as inhibition constantBinding affinity to CCR1 (unknown origin) assessed as inhibition constant
ChEMBL 351 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.4c02102
12093167 327835 32 None -1 2 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 351 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4475389 327835 32 None -1 2 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 351 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
10743274 238079 0 None None None Human 6.8 pKi = 6.8 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 478 7 1 3 6.3 N#CC(CCCN1CCC(O)(c2ccc(C(F)(F)F)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL344075 238079 0 None None None Human 6.8 pKi = 6.8 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 478 7 1 3 6.3 N#CC(CCCN1CCC(O)(c2ccc(C(F)(F)F)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
68551780 348208 0 None None None Human 6.8 pKi = 6.8 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 418 5 1 6 3.5 COc1cc(N2CCC(C(O)Cn3nc(C(F)(F)F)nc3C)CC2)ccc1Cl nan
CHEMBL4546480 348208 0 None None None Human 6.8 pKi = 6.8 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 418 5 1 6 3.5 COc1cc(N2CCC(C(O)Cn3nc(C(F)(F)F)nc3C)CC2)ccc1Cl nan
10833944 237552 0 None None None Human 6.8 pKi = 6.8 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 384 6 2 4 4.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(O)c1 10.1021/jm990316l
CHEMBL341840 237552 0 None None None Human 6.8 pKi = 6.8 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 384 6 2 4 4.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(O)c1 10.1021/jm990316l
71214710 174967 0 None -100 3 Human 5.8 pKi = 5.8 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 431 5 1 6 3.6 Cn1nnnc1Cc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207085 174967 0 None -100 3 Human 5.8 pKi = 5.8 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 431 5 1 6 3.6 Cn1nnnc1Cc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
71452487 174970 0 None -15 3 Human 5.8 pKi = 5.8 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 382 5 1 5 3.4 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1cccc(Cl)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207088 174970 0 None -15 3 Human 5.8 pKi = 5.8 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 382 5 1 5 3.4 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1cccc(Cl)c1 10.1016/j.bmcl.2012.09.020
71454247 174972 0 None -15 2 Human 5.8 pKi = 5.8 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 366 5 1 5 2.9 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1cccc(F)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207090 174972 0 None -15 2 Human 5.8 pKi = 5.8 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 366 5 1 5 2.9 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1cccc(F)c1 10.1016/j.bmcl.2012.09.020
71456008 174977 0 None -25 3 Human 5.8 pKi = 5.8 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 404 5 1 6 4.0 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1csc2ccccc12 10.1016/j.bmcl.2012.09.020
CHEMBL2207095 174977 0 None -25 3 Human 5.8 pKi = 5.8 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 404 5 1 6 4.0 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1csc2ccccc12 10.1016/j.bmcl.2012.09.020
3798520 334998 7 None None None Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 307 3 1 3 3.5 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccccc1 10.1021/acs.jmedchem.8b00605
CHEMBL4448679 334998 7 None None None Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 307 3 1 3 3.5 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccccc1 10.1021/acs.jmedchem.8b00605
3798520 334998 7 None None None Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 307 3 1 3 3.5 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccccc1 10.1021/acs.jmedchem.8b00605
CHEMBL4448679 334998 7 None None None Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 307 3 1 3 3.5 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccccc1 10.1021/acs.jmedchem.8b00605
3063068 66875 1 None None None Human 6.8 pKi = 6.8 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 468 5 1 4 6.2 Cc1ccccc1C1(O)CCN(CCCC2(C#N)c3ccccc3CSc3ccccc32)CC1 10.1021/jm990316l
CHEMBL141829 66875 1 None None None Human 6.8 pKi = 6.8 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 468 5 1 4 6.2 Cc1ccccc1C1(O)CCN(CCCC2(C#N)c3ccccc3CSc3ccccc32)CC1 10.1021/jm990316l
9967166 334536 7 None -2 2 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 4 1 3 3.9 CCc1ccc(N2C(=O)C(O)=C(C(C)=O)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4441958 334536 7 None -2 2 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 4 1 3 3.9 CCc1ccc(N2C(=O)C(O)=C(C(C)=O)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
9967166 334536 7 None -2 2 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 4 1 3 3.9 CCc1ccc(N2C(=O)C(O)=C(C(C)=O)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4441958 334536 7 None -2 2 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 4 1 3 3.9 CCc1ccc(N2C(=O)C(O)=C(C(C)=O)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
155535265 336546 0 None 8 2 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 339 4 1 3 4.1 Cc1ccc(N2C(=O)C(O)=C(C(=O)C3CC3)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4471583 336546 0 None 8 2 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 339 4 1 3 4.1 Cc1ccc(N2C(=O)C(O)=C(C(=O)C3CC3)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
155532102 336259 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 385 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1cccc(Br)c1 10.1021/acs.jmedchem.8b00605
CHEMBL4467095 336259 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 385 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1cccc(Br)c1 10.1021/acs.jmedchem.8b00605
155532102 336259 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 385 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1cccc(Br)c1 10.1021/acs.jmedchem.8b00605
CHEMBL4467095 336259 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 385 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1cccc(Br)c1 10.1021/acs.jmedchem.8b00605
155535265 336546 0 None 8 2 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 339 4 1 3 4.1 Cc1ccc(N2C(=O)C(O)=C(C(=O)C3CC3)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4471583 336546 0 None 8 2 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 339 4 1 3 4.1 Cc1ccc(N2C(=O)C(O)=C(C(=O)C3CC3)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
155561022 349004 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 321 3 1 3 3.8 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccc(C)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4566226 349004 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 321 3 1 3 3.8 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccc(C)cc1 10.1021/acs.jmedchem.8b00605
155553428 348249 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1cccc(Cl)c1 10.1021/acs.jmedchem.8b00605
CHEMBL4547735 348249 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1cccc(Cl)c1 10.1021/acs.jmedchem.8b00605
155561022 349004 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 321 3 1 3 3.8 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccc(C)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4566226 349004 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 321 3 1 3 3.8 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccc(C)cc1 10.1021/acs.jmedchem.8b00605
54712652 334545 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 343 4 1 4 3.7 CCOC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4442093 334545 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 343 4 1 4 3.7 CCOC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
155553428 348249 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1cccc(Cl)c1 10.1021/acs.jmedchem.8b00605
CHEMBL4547735 348249 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1cccc(Cl)c1 10.1021/acs.jmedchem.8b00605
71463166 174978 0 None -7 2 Human 5.7 pKi = 5.7 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 390 5 1 8 2.3 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1cccc2nonc12 10.1016/j.bmcl.2012.09.020
CHEMBL2207096 174978 0 None -7 2 Human 5.7 pKi = 5.7 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 390 5 1 8 2.3 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1cccc2nonc12 10.1016/j.bmcl.2012.09.020
57889188 233483 0 None None None Human 8.7 pKi = 8.7 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 437 6 3 3 3.9 CC[C@@H](C)NC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C nan
CHEMBL3334816 233483 0 None None None Human 8.7 pKi = 8.7 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 437 6 3 3 3.9 CC[C@@H](C)NC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C nan
71462570 163992 0 None -2 3 Human 8.6 pKi = 8.6 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 518 5 2 5 5.6 CC1(C)CN(CC/C=C2/c3cc(C(=O)O)ccc3OCc3ncccc32)C[C@H](c2ccc(Cl)cc2)[C@H]1O 10.1021/jm300682j
CHEMBL2178569 163992 0 None -2 3 Human 8.6 pKi = 8.6 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 518 5 2 5 5.6 CC1(C)CN(CC/C=C2/c3cc(C(=O)O)ccc3OCc3ncccc32)C[C@H](c2ccc(Cl)cc2)[C@H]1O 10.1021/jm300682j
57889334 181984 0 None None None Human 8.6 pKi = 8.6 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 422 6 2 3 4.0 CC(C)CC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C nan
CHEMBL2398743 181984 0 None None None Human 8.6 pKi = 8.6 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 422 6 2 3 4.0 CC(C)CC(=O)N[C@@H](C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1)C(C)C nan
54712652 334545 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 343 4 1 4 3.7 CCOC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4442093 334545 0 None None None Human 6.7 pKi = 6.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 343 4 1 4 3.7 CCOC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
3063066 67365 0 None None None Human 6.7 pKi = 6.7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 454 5 1 4 5.9 N#CC1(CCCN2CCC(O)(c3ccccc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
CHEMBL142244 67365 0 None None None Human 6.7 pKi = 6.7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 454 5 1 4 5.9 N#CC1(CCCN2CCC(O)(c3ccccc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
10695080 26473 0 None None None Human 6.7 pKi = 6.7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 418 6 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc2ccccc2c1 10.1021/jm990316l
CHEMBL1184276 26473 0 None None None Human 6.7 pKi = 6.7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 418 6 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc2ccccc2c1 10.1021/jm990316l
10645313 65924 0 None None None Human 6.7 pKi = 6.7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 411 7 1 4 4.7 N#CC(CCCN1CCC(O)(c2cccnc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL141020 65924 0 None None None Human 6.7 pKi = 6.7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 411 7 1 4 4.7 N#CC(CCCN1CCC(O)(c2cccnc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
10132885 349159 0 None 7 2 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 355 3 1 3 4.7 Cc1ccc(N2C(=O)C(O)=C(C(=O)C(C)(C)C)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4569870 349159 0 None 7 2 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 355 3 1 3 4.7 Cc1ccc(N2C(=O)C(O)=C(C(=O)C(C)(C)C)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
10132885 349159 0 None 7 2 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 355 3 1 3 4.7 Cc1ccc(N2C(=O)C(O)=C(C(=O)C(C)(C)C)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4569870 349159 0 None 7 2 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 355 3 1 3 4.7 Cc1ccc(N2C(=O)C(O)=C(C(=O)C(C)(C)C)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
10076510 25915 0 None None None Human 7.7 pKi = 7.7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 433 6 1 2 6.0 C[N+]1(CCCC(C#N)c2ccc3ccccc3c2)CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
CHEMBL1180795 25915 0 None None None Human 7.7 pKi = 7.7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 433 6 1 2 6.0 C[N+]1(CCCC(C#N)c2ccc3ccccc3c2)CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
9850002 78565 0 None None None Human 7.7 pKi = 7.7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 532 5 1 4 6.6 N#CC1(CCCN2CCC(O)(c3ccc(Br)cc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
CHEMBL143350 78565 0 None None None Human 7.7 pKi = 7.7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 532 5 1 4 6.6 N#CC1(CCCN2CCC(O)(c3ccc(Br)cc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
68556971 335034 0 None None None Human 5.7 pKi = 5.7 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 474 7 2 6 3.3 COc1cc(N2CCC(C(Cn3nc(C(F)(F)F)cc3C)NC(=O)CO)CC2)ccc1Cl nan
CHEMBL4449145 335034 0 None None None Human 5.7 pKi = 5.7 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 474 7 2 6 3.3 COc1cc(N2CCC(C(Cn3nc(C(F)(F)F)cc3C)NC(=O)CO)CC2)ccc1Cl nan
68556936 336854 0 None None None Human 5.7 pKi = 5.7 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 401 5 2 7 3.0 COc1cc(N2CCC(C(O)Cn3nc(N)c4cccnc43)CC2)ccc1Cl nan
CHEMBL4475524 336854 0 None None None Human 5.7 pKi = 5.7 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 401 5 2 7 3.0 COc1cc(N2CCC(C(O)Cn3nc(N)c4cccnc43)CC2)ccc1Cl nan
10530837 78923 0 None None None Human 6.7 pKi = 6.7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 556 5 1 4 7.5 N#CC1(CCCN2CCC(O)(c3ccc(Cl)c(C(F)(F)F)c3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
CHEMBL143814 78923 0 None None None Human 6.7 pKi = 6.7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 556 5 1 4 7.5 N#CC1(CCCN2CCC(O)(c3ccc(Cl)c(C(F)(F)F)c3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
10293022 335639 7 None -1 2 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 377 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4457687 335639 7 None -1 2 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 377 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
10554359 77766 0 None None None Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 536 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(I)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL142676 77766 0 None None None Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 536 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(I)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
10766333 78619 0 None None None Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 458 5 1 4 6.0 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2Oc2ccccc21 10.1021/jm990316l
CHEMBL143449 78619 0 None None None Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 458 5 1 4 6.0 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2Oc2ccccc21 10.1021/jm990316l
10690854 66372 0 None None None Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 374 6 1 4 4.8 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccsc1 10.1021/jm990316l
CHEMBL141387 66372 0 None None None Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 374 6 1 4 4.8 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccsc1 10.1021/jm990316l
10293022 335639 7 None -1 2 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 377 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4457687 335639 7 None -1 2 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 377 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
5311125 78652 0 None None None Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 488 5 1 4 6.5 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
CHEMBL143492 78652 0 None None None Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 488 5 1 4 6.5 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
10623381 40784 0 None None None Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 448 8 2 3 5.3 NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL125111 40784 0 None None None Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 448 8 2 3 5.3 NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
12093162 347425 0 None -1 2 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 329 4 1 4 3.4 COc1ccc(N2C(=O)C(O)=C(C(C)=O)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4526524 347425 0 None -1 2 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 329 4 1 4 3.4 COc1ccc(N2C(=O)C(O)=C(C(C)=O)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
71457815 174973 0 None -50 3 Human 5.6 pKi = 5.6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 416 5 1 5 3.8 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1cccc(C(F)(F)F)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207091 174973 0 None -50 3 Human 5.6 pKi = 5.6 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 416 5 1 5 3.8 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1cccc(C(F)(F)F)c1 10.1016/j.bmcl.2012.09.020
12093162 347425 0 None -1 2 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 329 4 1 4 3.4 COc1ccc(N2C(=O)C(O)=C(C(C)=O)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4526524 347425 0 None -1 2 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 329 4 1 4 3.4 COc1ccc(N2C(=O)C(O)=C(C(C)=O)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
9967349 347178 0 None 1 2 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 331 3 1 3 3.8 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4519533 347178 0 None 1 2 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 331 3 1 3 3.8 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
155559153 348818 0 None 2 2 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 457 4 1 3 5.6 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1)c1ccccc1 10.1021/acs.jmedchem.8b00605
CHEMBL4561618 348818 0 None 2 2 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 457 4 1 3 5.6 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1)c1ccccc1 10.1021/acs.jmedchem.8b00605
155559153 348818 0 None 2 2 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 457 4 1 3 5.6 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1)c1ccccc1 10.1021/acs.jmedchem.8b00605
CHEMBL4561618 348818 0 None 2 2 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 457 4 1 3 5.6 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1)c1ccccc1 10.1021/acs.jmedchem.8b00605
9902578 335894 0 None 4 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 5 1 3 4.5 CCCC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4461627 335894 0 None 4 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 5 1 3 4.5 CCCC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
9902578 335894 0 None 4 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 5 1 3 4.5 CCCC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4461627 335894 0 None 4 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 5 1 3 4.5 CCCC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
9967349 347178 0 None 1 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 331 3 1 3 3.8 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4519533 347178 0 None 1 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 331 3 1 3 3.8 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2F)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
44361881 333207 0 None None None Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 500 5 1 3 5.9 N#CC1(CCCN2CCC(O)(c3ccc(Br)cc3)CC2)c2ccccc2Cc2ccccc21 10.1021/jm990316l
CHEMBL435485 333207 0 None None None Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 500 5 1 3 5.9 N#CC1(CCCN2CCC(O)(c3ccc(Br)cc3)CC2)c2ccccc2Cc2ccccc21 10.1021/jm990316l
24764465 349756 0 None None None Human 8.5 pKi = 8.5 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 556 7 2 6 5.0 COc1cc(N2CCC(C(Cn3nc(C(F)(F)F)c(Cl)c3C)NC(=O)[C@@H](C)O)CC2)c(Cl)cc1Cl nan
CHEMBL4583778 349756 0 None None None Human 8.5 pKi = 8.5 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 556 7 2 6 5.0 COc1cc(N2CCC(C(Cn3nc(C(F)(F)F)c(Cl)c3C)NC(=O)[C@@H](C)O)CC2)c(Cl)cc1Cl nan
44537841 1390 22 None None None Human 8.4 pKi = 8.4 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C nan
57889181 1390 22 None None None Human 8.4 pKi = 8.4 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C nan
9497 1390 22 None None None Human 8.4 pKi = 8.4 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C nan
CHEMBL2398716 1390 22 None None None Human 8.4 pKi = 8.4 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C nan
CHEMBL3334824 1390 22 None None None Human 8.4 pKi = 8.4 Binding
Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.Binding Assay: For radioligand competition studies, a final concentration of 1x105 THP-1 monocytic leukemia cells are combined with 100 μg of LS WGA PS beads (Amersham, Cat.#: RPNQ 0260) in 40 μL of assay buffer (RPMI 1640 without phenol red, 50 mM HEPES, 5 mM MgCl2, 1 mM CaCl2, 0.1% BSA). The THP-1 cell/bead mixture was added to each well of a 384-well assay plate (PerkinElmer, Cat. #:6007899) containing test compound in 3-fold serial dilution, with final concentrations ranging from 8 μM to 0.14 nM. A final concentration of 0.1 nM [125I]-MIP-1α (PerkinElmer, Cat. #NEX298) in 20 μL assay buffer was added to the reaction. Unlabeled MIP-1α was added in excess to some wells to determine non-specific binding. Sealed assay plates were incubated at room temperature for 12 h then analyzed by LEADseeker.
ChEMBL 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C nan
155539148 346931 0 None 3 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 4 1 3 4.1 CCC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4513770 346931 0 None 3 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 4 1 3 4.1 CCC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
155539148 346931 0 None 3 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 4 1 3 4.1 CCC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4513770 346931 0 None 3 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 4 1 3 4.1 CCC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
22725647 347783 0 None -3 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 347 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)c(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4535696 347783 0 None -3 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 347 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)c(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
10501338 239661 0 None None None Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 402 6 1 3 5.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1Cl 10.1021/jm990316l
CHEMBL356764 239661 0 None None None Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 402 6 1 3 5.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1Cl 10.1021/jm990316l
155545804 347591 0 None 5 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 355 6 1 3 4.9 CCCCC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4530510 347591 0 None 5 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 355 6 1 3 4.9 CCCCC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
22725647 347783 0 None -3 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 347 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)c(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4535696 347783 0 None -3 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 347 3 1 3 4.3 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)c(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
155545804 347591 0 None 5 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 355 6 1 3 4.9 CCCCC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4530510 347591 0 None 5 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 355 6 1 3 4.9 CCCCC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
71450658 174980 0 None -31 3 Human 6.5 pKi = 6.5 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 450 5 1 5 4.7 O=S(=O)(Nc1cc(Cl)c(Cl)cc1Cn1ccnn1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207098 174980 0 None -31 3 Human 6.5 pKi = 6.5 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 450 5 1 5 4.7 O=S(=O)(Nc1cc(Cl)c(Cl)cc1Cn1ccnn1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
71454248 174983 0 None -25 3 Human 6.5 pKi = 6.5 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 422 5 1 6 4.1 O=S(=O)(Nc1cc(Cl)c(Cl)cc1Cn1ccnn1)c1ccc(Cl)s1 10.1016/j.bmcl.2012.09.020
CHEMBL2207100 174983 0 None -25 3 Human 6.5 pKi = 6.5 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 422 5 1 6 4.1 O=S(=O)(Nc1cc(Cl)c(Cl)cc1Cn1ccnn1)c1ccc(Cl)s1 10.1016/j.bmcl.2012.09.020
10649043 78046 0 None None None Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 499 5 1 4 5.5 CN1C(=O)c2ccccc2C(C#N)(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc21 10.1021/jm990316l
CHEMBL142925 78046 0 None None None Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 499 5 1 4 5.5 CN1C(=O)c2ccccc2C(C#N)(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc21 10.1021/jm990316l
10717972 238111 0 None None None Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 440 8 1 5 4.4 CCOC(=O)C(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
CHEMBL344324 238111 0 None None None Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 440 8 1 5 4.4 CCOC(=O)C(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
10647579 78866 0 None None None Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 458 6 1 3 5.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1c(F)c(F)c(F)c(F)c1F 10.1021/jm990316l
CHEMBL143772 78866 0 None None None Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 458 6 1 3 5.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1c(F)c(F)c(F)c(F)c1F 10.1021/jm990316l
9956488 238012 0 None None None Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 472 5 1 4 5.8 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2COc2ccccc21 10.1021/jm990316l
CHEMBL343511 238012 0 None None None Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 472 5 1 4 5.8 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2COc2ccccc21 10.1021/jm990316l
10672205 238137 0 None None None Human 5.5 pKi = 5.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 474 9 1 4 6.3 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(OCc2ccccc2)cc1 10.1021/jm990316l
CHEMBL344499 238137 0 None None None Human 5.5 pKi = 5.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 474 9 1 4 6.3 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(OCc2ccccc2)cc1 10.1021/jm990316l
10670785 66739 0 None None None Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 440 8 1 4 5.3 COc1ccc(C2(O)CCN(CCCC(C#N)(c3ccccc3)c3ccccc3)CC2)cc1 10.1021/jm990316l
CHEMBL141713 66739 0 None None None Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 440 8 1 4 5.3 COc1ccc(C2(O)CCN(CCCC(C#N)(c3ccccc3)c3ccccc3)CC2)cc1 10.1021/jm990316l
44199443 335090 0 None None None Human 6.5 pKi = 6.5 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 378 6 2 3 4.0 CCC(NC(=O)C1CCCC1)C(O)C1CCN(c2ccc(Cl)cc2)CC1 nan
CHEMBL4449875 335090 0 None None None Human 6.5 pKi = 6.5 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 378 6 2 3 4.0 CCC(NC(=O)C1CCCC1)C(O)C1CCN(c2ccc(Cl)cc2)CC1 nan
10597049 66859 0 None None None Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 398 7 1 4 4.7 COc1ccc(C(C#N)CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1 10.1021/jm990316l
CHEMBL141817 66859 0 None None None Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 398 7 1 4 4.7 COc1ccc(C(C#N)CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1 10.1021/jm990316l
10837160 239734 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 446 6 1 3 5.5 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1Br 10.1021/jm990316l
CHEMBL357445 239734 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 446 6 1 3 5.5 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1Br 10.1021/jm990316l
10596333 67268 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 386 6 1 3 4.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1F 10.1021/jm990316l
CHEMBL142160 67268 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 386 6 1 3 4.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1F 10.1021/jm990316l
9902204 334685 6 None -2 2 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 333 3 1 3 4.0 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4443909 334685 6 None -2 2 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 333 3 1 3 4.0 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
10503474 77800 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 444 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2cccc(Cl)c2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL142713 77800 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 444 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2cccc(Cl)c2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
15985912 174963 0 None -9 3 Human 6.4 pKi = 6.4 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 416 5 1 5 4.1 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207081 174963 0 None -9 3 Human 6.4 pKi = 6.4 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 416 5 1 5 4.1 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
71214709 174966 0 None -14 2 Human 6.4 pKi = 6.4 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 431 5 1 6 3.8 Cc1nnnn1Cc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207084 174966 0 None -14 2 Human 6.4 pKi = 6.4 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 431 5 1 6 3.8 Cc1nnnn1Cc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
71454246 174971 0 None -7 3 Human 5.4 pKi = 5.4 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 376 5 1 5 3.4 Cc1ccc(S(=O)(=O)Nc2cc(Cl)ccc2Cn2ccnn2)cc1C 10.1016/j.bmcl.2012.09.020
CHEMBL2207089 174971 0 None -7 3 Human 5.4 pKi = 5.4 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 376 5 1 5 3.4 Cc1ccc(S(=O)(=O)Nc2cc(Cl)ccc2Cn2ccnn2)cc1C 10.1016/j.bmcl.2012.09.020
87494453 348986 0 None None None Human 8.4 pKi = 8.4 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 544 7 1 5 5.6 COc1cc(N2CCC(C(Cn3nc(C(F)(F)F)c(Cl)c3C)NC(=O)CF)CC2)c(Cl)cc1Cl nan
CHEMBL4565880 348986 0 None None None Human 8.4 pKi = 8.4 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 544 7 1 5 5.6 COc1cc(N2CCC(C(Cn3nc(C(F)(F)F)c(Cl)c3C)NC(=O)CF)CC2)c(Cl)cc1Cl nan
9902204 334685 6 None -2 2 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 333 3 1 3 4.0 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4443909 334685 6 None -2 2 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 333 3 1 3 4.0 CC(=O)C1=C(O)C(=O)N(c2ccc(Cl)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
155513751 334368 0 None 7 2 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 4 1 3 4.3 Cc1ccc(N2C(=O)C(O)=C(C(=O)C(C)C)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4439354 334368 0 None 7 2 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 4 1 3 4.3 Cc1ccc(N2C(=O)C(O)=C(C(=O)C(C)C)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
10694874 78460 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 450 7 1 3 6.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)C1CCCCC1 10.1021/jm990316l
CHEMBL143266 78460 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 450 7 1 3 6.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)C1CCCCC1 10.1021/jm990316l
10524463 329801 0 None None None Human 5.4 pKi = 5.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 390 9 1 3 5.3 CCCCC1(O)CCN(CCCC(C#N)(c2ccccc2)c2ccccc2)CC1 10.1021/jm990316l
CHEMBL422115 329801 0 None None None Human 5.4 pKi = 5.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 390 9 1 3 5.3 CCCCC1(O)CCN(CCCC(C#N)(c2ccccc2)c2ccccc2)CC1 10.1021/jm990316l
10838033 237872 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 468 6 1 4 6.0 N#CC1(CCCN2CCC(O)(Cc3ccccc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
CHEMBL342721 237872 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 468 6 1 4 6.0 N#CC1(CCCN2CCC(O)(Cc3ccccc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
10814504 239657 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 477 8 1 4 5.6 COC(=O)C(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL356718 239657 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 477 8 1 4 5.6 COC(=O)C(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
9845614 239888 19 None None None Human 5.4 pKi = 5.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 430 6 1 3 5.5 N#CC(CCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL357919 239888 19 None None None Human 5.4 pKi = 5.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 430 6 1 3 5.5 N#CC(CCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
155513751 334368 0 None 7 2 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 4 1 3 4.3 Cc1ccc(N2C(=O)C(O)=C(C(=O)C(C)C)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4439354 334368 0 None 7 2 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 4 1 3 4.3 Cc1ccc(N2C(=O)C(O)=C(C(=O)C(C)C)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
22335694 336091 0 None -2 2 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 3 1 3 4.0 CC(=O)C1=C(O)C(=O)N(c2ccc(C)c(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4464639 336091 0 None -2 2 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 3 1 3 4.0 CC(=O)C1=C(O)C(=O)N(c2ccc(C)c(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
10571296 78952 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 371 6 1 4 4.0 Cn1cccc1C(C#N)CCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
CHEMBL143840 78952 0 None None None Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 371 6 1 4 4.0 Cn1cccc1C(C#N)CCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
22335694 336091 0 None -2 2 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 3 1 3 4.0 CC(=O)C1=C(O)C(=O)N(c2ccc(C)c(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4464639 336091 0 None -2 2 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 3 1 3 4.0 CC(=O)C1=C(O)C(=O)N(c2ccc(C)c(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
9804868 67454 1 None None None Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 472 5 1 4 6.0 N#CC1(CCCN2CCC(O)(c3ccc(F)cc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
CHEMBL142318 67454 1 None None None Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 472 5 1 4 6.0 N#CC1(CCCN2CCC(O)(c3ccc(F)cc3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
9956380 332961 0 None None None Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 470 5 1 3 6.0 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2CCc2ccccc21 10.1021/jm990316l
CHEMBL433746 332961 0 None None None Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 470 5 1 3 6.0 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2CCc2ccccc21 10.1021/jm990316l
10786180 78936 0 None None None Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 382 6 1 3 4.9 CC(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
CHEMBL143825 78936 0 None None None Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 382 6 1 3 4.9 CC(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
10573219 79060 0 None None None Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 402 6 1 3 5.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)cc1 10.1021/jm990316l
CHEMBL143942 79060 0 None None None Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 402 6 1 3 5.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(Cl)cc1 10.1021/jm990316l
22335665 347564 0 None 1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 331 3 1 3 3.8 CC(=O)C1=C(O)C(=O)N(c2ccc(C)c(F)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4529804 347564 0 None 1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 331 3 1 3 3.8 CC(=O)C1=C(O)C(=O)N(c2ccc(C)c(F)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
12093163 348453 0 None -1 2 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 313 3 1 3 3.7 CC(=O)C1=C(O)C(=O)N(c2cccc(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4552420 348453 0 None -1 2 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 313 3 1 3 3.7 CC(=O)C1=C(O)C(=O)N(c2cccc(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
22335665 347564 0 None 1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 331 3 1 3 3.8 CC(=O)C1=C(O)C(=O)N(c2ccc(C)c(F)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4529804 347564 0 None 1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 331 3 1 3 3.8 CC(=O)C1=C(O)C(=O)N(c2ccc(C)c(F)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
10695227 78802 0 None None None Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 458 9 1 6 4.7 COc1cc(C(C#N)CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc(OC)c1OC 10.1021/jm990316l
CHEMBL143690 78802 0 None None None Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 458 9 1 6 4.7 COc1cc(C(C#N)CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc(OC)c1OC 10.1021/jm990316l
10195332 163993 0 None None None Human 8.3 pKi = 8.3 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 461 9 4 6 3.4 CC(=O)Nc1ccc(O)cc1OC[C@@](C)(O)CNC1CCN(Cc2ccc(Cl)cc2)CC1 10.1021/jm300682j
CHEMBL2178570 163993 0 None None None Human 8.3 pKi = 8.3 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 461 9 4 6 3.4 CC(=O)Nc1ccc(O)cc1OC[C@@](C)(O)CNC1CCN(Cc2ccc(Cl)cc2)CC1 10.1021/jm300682j
2352 195309 69 None None None Human 8.3 pKi = 8.3 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 444 6 3 9 0.9 Cc1nnc(C(=O)NC(C)(C)c2nc(C(=O)NCc3ccc(F)cc3)c(O)c(=O)n2C)o1 10.1021/jm300682j
54671008 195309 69 None None None Human 8.3 pKi = 8.3 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 444 6 3 9 0.9 Cc1nnc(C(=O)NC(C)(C)c2nc(C(=O)NCc3ccc(F)cc3)c(O)c(=O)n2C)o1 10.1021/jm300682j
CHEMBL254316 195309 69 None None None Human 8.3 pKi = 8.3 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 444 6 3 9 0.9 Cc1nnc(C(=O)NC(C)(C)c2nc(C(=O)NCc3ccc(F)cc3)c(O)c(=O)n2C)o1 10.1021/jm300682j
DB06817 195309 69 None None None Human 8.3 pKi = 8.3 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 444 6 3 9 0.9 Cc1nnc(C(=O)NC(C)(C)c2nc(C(=O)NCc3ccc(F)cc3)c(O)c(=O)n2C)o1 10.1021/jm300682j
155521447 335135 0 None 2 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 421 4 1 3 4.7 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1)C1CC1 10.1021/acs.jmedchem.8b00605
CHEMBL4450561 335135 0 None 2 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 421 4 1 3 4.7 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1)C1CC1 10.1021/acs.jmedchem.8b00605
87496446 335323 0 None None None Human 8.3 pKi = 8.3 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 542 7 2 6 4.6 COc1cc(N2CCC(C(Cn3nc(C(F)(F)F)c(Cl)c3C)NC(=O)CO)CC2)c(Cl)cc1Cl nan
CHEMBL4452884 335323 0 None None None Human 8.3 pKi = 8.3 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 542 7 2 6 4.6 COc1cc(N2CCC(C(Cn3nc(C(F)(F)F)c(Cl)c3C)NC(=O)CO)CC2)c(Cl)cc1Cl nan
155521447 335135 0 None 2 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 421 4 1 3 4.7 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1)C1CC1 10.1021/acs.jmedchem.8b00605
CHEMBL4450561 335135 0 None 2 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 421 4 1 3 4.7 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1C1CCCCC1)C1CC1 10.1021/acs.jmedchem.8b00605
155514261 334402 0 None None None Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 493 4 1 3 5.2 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1c1cccc(Br)c1)C1CC1 10.1021/acs.jmedchem.8b00605
CHEMBL4439854 334402 0 None None None Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 493 4 1 3 5.2 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1c1cccc(Br)c1)C1CC1 10.1021/acs.jmedchem.8b00605
155514261 334402 0 None None None Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 493 4 1 3 5.2 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1c1cccc(Br)c1)C1CC1 10.1021/acs.jmedchem.8b00605
CHEMBL4439854 334402 0 None None None Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 493 4 1 3 5.2 O=C(C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1c1cccc(Br)c1)C1CC1 10.1021/acs.jmedchem.8b00605
12093163 348453 0 None -1 2 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 313 3 1 3 3.7 CC(=O)C1=C(O)C(=O)N(c2cccc(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4552420 348453 0 None -1 2 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 313 3 1 3 3.7 CC(=O)C1=C(O)C(=O)N(c2cccc(C)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
15985914 174962 0 None -8 2 Human 6.3 pKi = 6.3 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 457 6 1 6 4.4 O=S(=O)(Nc1cc(Cl)ccc1Cn1nnnc1C1CC1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207080 174962 0 None -8 2 Human 6.3 pKi = 6.3 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 457 6 1 6 4.4 O=S(=O)(Nc1cc(Cl)ccc1Cn1nnnc1C1CC1)c1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2012.09.020
71450657 174976 0 None -19 3 Human 6.3 pKi = 6.3 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 422 5 1 6 4.1 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1cc(Cl)c(Cl)s1 10.1016/j.bmcl.2012.09.020
CHEMBL2207094 174976 0 None -19 3 Human 6.3 pKi = 6.3 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 422 5 1 6 4.1 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1cc(Cl)c(Cl)s1 10.1016/j.bmcl.2012.09.020
10789482 67301 0 None None None Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 444 9 1 3 5.9 N#CC(CCCCl)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
CHEMBL142191 67301 0 None None None Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 444 9 1 3 5.9 N#CC(CCCCl)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
10549688 330251 0 None None None Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 413 7 1 5 4.6 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc([N+](=O)[O-])c1 10.1021/jm990316l
CHEMBL423734 330251 0 None None None Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 413 7 1 5 4.6 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc([N+](=O)[O-])c1 10.1021/jm990316l
9889700 237386 15 None None None Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 444 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL34166 237386 15 None None None Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 444 7 1 3 5.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
9967465 336612 7 None -2 2 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 333 3 1 3 4.0 CC(=O)C1=C(O)C(=O)N(c2cccc(Cl)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4472384 336612 7 None -2 2 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 333 3 1 3 4.0 CC(=O)C1=C(O)C(=O)N(c2cccc(Cl)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
10764931 238036 0 None None None Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 426 7 1 5 4.0 COC(=O)C(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
CHEMBL343680 238036 0 None None None Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 426 7 1 5 4.0 COC(=O)C(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
10667913 67271 0 None None None Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 386 6 1 3 4.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(F)cc1 10.1021/jm990316l
CHEMBL142161 67271 0 None None None Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 386 6 1 3 4.9 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(F)cc1 10.1021/jm990316l
2868511 86047 10 None None None Human 6.3 pKi = 6.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 337 4 1 4 3.5 COc1ccc(C2C(C(C)=O)=C(O)C(=O)N2c2ccc(C)cc2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL1500746 86047 10 None None None Human 6.3 pKi = 6.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 337 4 1 4 3.5 COc1ccc(C2C(C(C)=O)=C(O)C(=O)N2c2ccc(C)cc2)cc1 10.1021/acs.jmedchem.8b00605
10499297 78225 0 None None None Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 368 6 1 3 4.7 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
CHEMBL143059 78225 0 None None None Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 368 6 1 3 4.7 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
9870787 78354 0 None None None Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 504 5 1 4 5.5 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2C[S+]([O-])c2ccccc21 10.1021/jm990316l
CHEMBL143173 78354 0 None None None Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 504 5 1 4 5.5 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2C[S+]([O-])c2ccccc21 10.1021/jm990316l
9857981 335332 7 None 1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 313 3 1 3 3.7 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4453024 335332 7 None 1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 313 3 1 3 3.7 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
9945265 335724 0 None 1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4459033 335724 0 None 1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCCC1 10.1021/acs.jmedchem.8b00605
2868511 86047 10 None None None Human 6.3 pKi = 6.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 337 4 1 4 3.5 COc1ccc(C2C(C(C)=O)=C(O)C(=O)N2c2ccc(C)cc2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL1500746 86047 10 None None None Human 6.3 pKi = 6.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 337 4 1 4 3.5 COc1ccc(C2C(C(C)=O)=C(O)C(=O)N2c2ccc(C)cc2)cc1 10.1021/acs.jmedchem.8b00605
9967465 336612 7 None -2 2 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 333 3 1 3 4.0 CC(=O)C1=C(O)C(=O)N(c2cccc(Cl)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4472384 336612 7 None -2 2 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 333 3 1 3 4.0 CC(=O)C1=C(O)C(=O)N(c2cccc(Cl)c2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
9857981 335332 7 None 1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 313 3 1 3 3.7 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4453024 335332 7 None 1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 313 3 1 3 3.7 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCC1 10.1021/acs.jmedchem.8b00605
9945265 335724 0 None 1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4459033 335724 0 None 1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 327 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCCC1 10.1021/acs.jmedchem.8b00605
9869274 238077 0 None None None Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 468 5 1 3 6.4 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2C=Cc2ccccc21 10.1021/jm990316l
CHEMBL344073 238077 0 None None None Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 468 5 1 3 6.4 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2C=Cc2ccccc21 10.1021/jm990316l
9924108 336304 0 None 2 2 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 3 1 3 4.5 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4467708 336304 0 None 2 2 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 3 1 3 4.5 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCCCC1 10.1021/acs.jmedchem.8b00605
9924108 336304 0 None 2 2 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 3 1 3 4.5 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCCCC1 10.1021/acs.jmedchem.8b00605
CHEMBL4467708 336304 0 None 2 2 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 3 1 3 4.5 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1C1CCCCCCC1 10.1021/acs.jmedchem.8b00605
10737864 240173 0 None None None Human 6.2 pKi = 6.2 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 369 6 1 4 4.1 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccn1 10.1021/jm990316l
CHEMBL358596 240173 0 None None None Human 6.2 pKi = 6.2 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 369 6 1 4 4.1 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccn1 10.1021/jm990316l
11801020 26518 0 None None None Human 8.2 pKi = 8.2 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 434 7 1 1 6.4 C[N+]1(CCCC(c2ccccc2)c2ccccc2)CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
CHEMBL1184558 26518 0 None None None Human 8.2 pKi = 8.2 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 434 7 1 1 6.4 C[N+]1(CCCC(c2ccccc2)c2ccccc2)CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
24863549 334962 0 None None None Human 8.2 pKi = 8.2 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 526 6 1 5 5.6 COc1cc(N2CCC(C(Cn3nc(C(F)(F)F)c(Cl)c3C)NC(C)=O)CC2)c(Cl)cc1Cl nan
CHEMBL4448154 334962 0 None None None Human 8.2 pKi = 8.2 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 526 6 1 5 5.6 COc1cc(N2CCC(C(Cn3nc(C(F)(F)F)c(Cl)c3C)NC(C)=O)CC2)c(Cl)cc1Cl nan
10768343 237538 0 None None None Human 6.2 pKi = 6.2 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 522 5 1 4 6.9 N#CC1(CCCN2CCC(O)(c3cccc(C(F)(F)F)c3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
CHEMBL341769 237538 0 None None None Human 6.2 pKi = 6.2 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 522 5 1 4 6.9 N#CC1(CCCN2CCC(O)(c3cccc(C(F)(F)F)c3)CC2)c2ccccc2CSc2ccccc21 10.1021/jm990316l
155526680 335670 0 None 3 2 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 467 3 1 3 4.8 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1c1cccc(Br)c1 10.1021/acs.jmedchem.8b00605
CHEMBL4458295 335670 0 None 3 2 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 467 3 1 3 4.8 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1c1cccc(Br)c1 10.1021/acs.jmedchem.8b00605
155526680 335670 0 None 3 2 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 467 3 1 3 4.8 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1c1cccc(Br)c1 10.1021/acs.jmedchem.8b00605
CHEMBL4458295 335670 0 None 3 2 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 467 3 1 3 4.8 CC(=O)C1=C(O)C(=O)N(c2ccc(Br)cc2F)C1c1cccc(Br)c1 10.1021/acs.jmedchem.8b00605
3794409 335301 6 None 3 2 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccc(Cl)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4452558 335301 6 None 3 2 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccc(Cl)cc1 10.1021/acs.jmedchem.8b00605
3794409 335301 6 None 3 2 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccc(Cl)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4452558 335301 6 None 3 2 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 341 3 1 3 4.1 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccc(Cl)cc1 10.1021/acs.jmedchem.8b00605
9870787 78354 0 None None None Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 504 5 1 4 5.5 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2C[S+]([O-])c2ccccc21 10.1021/jm990316l
CHEMBL143173 78354 0 None None None Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 504 5 1 4 5.5 N#CC1(CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)c2ccccc2C[S+]([O-])c2ccccc21 10.1021/jm990316l
10813846 65055 0 None None None Human 6.2 pKi = 6.2 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 460 7 1 3 6.4 N#CC(CCCN1CCC(O)(c2ccc3ccccc3c2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL140270 65055 0 None None None Human 6.2 pKi = 6.2 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 460 7 1 3 6.4 N#CC(CCCN1CCC(O)(c2ccc3ccccc3c2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
3497 2447 26 None -1 3 Human 7.1 pKi = 7.1 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1021/jm300682j
44309353 2447 26 None -1 3 Human 7.1 pKi = 7.1 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1021/jm300682j
5311123 2447 26 None -1 3 Human 7.1 pKi = 7.1 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1021/jm300682j
CHEMBL1628706 2447 26 None -1 3 Human 7.1 pKi = 7.1 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1021/jm300682j
CHEMBL308473 2447 26 None -1 3 Human 7.1 pKi = 7.1 Binding
Binding affinity to CCR1Binding affinity to CCR1
ChEMBL 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 10.1021/jm300682j
10766998 77515 0 None None None Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 476 7 1 4 5.5 COc1ccc(C(C#N)CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1Br 10.1021/jm990316l
CHEMBL142468 77515 0 None None None Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 476 7 1 4 5.5 COc1ccc(C(C#N)CCCN2CCC(O)(c3ccc(Cl)cc3)CC2)cc1Br 10.1021/jm990316l
10693630 160348 0 None None None Human 5.1 pKi = 5.1 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 424 8 1 3 5.3 N#CC(CCCN1CCC(CO)(c2ccccc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL2112830 160348 0 None None None Human 5.1 pKi = 5.1 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 424 8 1 3 5.3 N#CC(CCCN1CCC(CO)(c2ccccc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
155548977 347872 0 None None None Human 7.1 pKi = 7.1 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 375 4 1 3 5.0 Cc1ccc(N2C(=O)C(O)=C(C(=O)c3ccccc3)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4538013 347872 0 None None None Human 7.1 pKi = 7.1 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 375 4 1 3 5.0 Cc1ccc(N2C(=O)C(O)=C(C(=O)c3ccccc3)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
155548977 347872 0 None None None Human 7.1 pKi = 7.1 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 375 4 1 3 5.0 Cc1ccc(N2C(=O)C(O)=C(C(=O)c3ccccc3)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4538013 347872 0 None None None Human 7.1 pKi = 7.1 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 375 4 1 3 5.0 Cc1ccc(N2C(=O)C(O)=C(C(=O)c3ccccc3)C2C2CCCCC2)cc1 10.1021/acs.jmedchem.8b00605
10575889 67305 0 None None None Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 458 8 1 3 6.3 N#CC(CCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL142199 67305 0 None None None Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 458 8 1 3 6.3 N#CC(CCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
10643770 77891 0 None None None Human 6.1 pKi = 6.1 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 384 6 2 4 4.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1O 10.1021/jm990316l
CHEMBL142798 77891 0 None None None Human 6.1 pKi = 6.1 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 384 6 2 4 4.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1O 10.1021/jm990316l
71463165 174968 0 None -6 2 Human 5.1 pKi = 5.1 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 348 5 1 5 2.8 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1ccccc1 10.1016/j.bmcl.2012.09.020
CHEMBL2207086 174968 0 None -6 2 Human 5.1 pKi = 5.1 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 348 5 1 5 2.8 O=S(=O)(Nc1cc(Cl)ccc1Cn1ccnn1)c1ccccc1 10.1016/j.bmcl.2012.09.020
71456007 174974 0 None -5 3 Human 5.1 pKi = 5.1 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 373 5 1 6 2.7 N#Cc1cccc(S(=O)(=O)Nc2cc(Cl)ccc2Cn2ccnn2)c1 10.1016/j.bmcl.2012.09.020
CHEMBL2207092 174974 0 None -5 3 Human 5.1 pKi = 5.1 Binding
Binding affinity to CCR1 by 35S-gamma-GTP membrane assayBinding affinity to CCR1 by 35S-gamma-GTP membrane assay
ChEMBL 373 5 1 6 2.7 N#Cc1cccc(S(=O)(=O)Nc2cc(Cl)ccc2Cn2ccnn2)c1 10.1016/j.bmcl.2012.09.020
10722083 144791 0 None None None Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 459 7 1 2 6.1 C[N+]1(CCCC(C#N)(c2ccccc2)c2ccccc2)CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
CHEMBL199252 144791 0 None None None Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 459 7 1 2 6.1 C[N+]1(CCCC(C#N)(c2ccccc2)c2ccccc2)CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
3796276 335395 6 None 2 2 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 385 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccc(Br)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4453953 335395 6 None 2 2 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 385 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccc(Br)cc1 10.1021/acs.jmedchem.8b00605
3796276 335395 6 None 2 2 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 385 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccc(Br)cc1 10.1021/acs.jmedchem.8b00605
CHEMBL4453953 335395 6 None 2 2 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometryDisplacement of [3H]-CCR2-RA-[R] from human TEV protease site linked CCR1 expressed in human U20S cell membranes co-expressing Gal4-VP16 transcription factor after 120 mins by scintillation spectrometry
ChEMBL 385 3 1 3 4.2 CC(=O)C1=C(O)C(=O)N(c2ccc(C)cc2)C1c1ccc(Br)cc1 10.1021/acs.jmedchem.8b00605
9959839 77841 0 None None None Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 574 10 4 4 5.4 O=C(NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1)NC1CCNCC1 10.1021/jm990316l
CHEMBL142752 77841 0 None None None Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 574 10 4 4 5.4 O=C(NCC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1)NC1CCNCC1 10.1021/jm990316l
10525695 240103 0 None None None Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 411 7 1 4 4.7 N#CC(CCCN1CCC(O)(c2ccccn2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL358283 240103 0 None None None Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 411 7 1 4 4.7 N#CC(CCCN1CCC(O)(c2ccccn2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
11798220 67386 0 None None None Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 460 8 1 4 6.5 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(Oc2ccccc2)c1 10.1021/jm990316l
CHEMBL142263 67386 0 None None None Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 460 8 1 4 6.5 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1cccc(Oc2ccccc2)c1 10.1021/jm990316l
10789018 78655 0 None None None Human 7.0 pKi = 7.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 435 7 1 4 5.1 N#Cc1ccc(C2(O)CCN(CCCC(C#N)(c3ccccc3)c3ccccc3)CC2)cc1 10.1021/jm990316l
CHEMBL143499 78655 0 None None None Human 7.0 pKi = 7.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 435 7 1 4 5.1 N#Cc1ccc(C2(O)CCN(CCCC(C#N)(c3ccccc3)c3ccccc3)CC2)cc1 10.1021/jm990316l
10548809 237945 0 None None None Human 7.0 pKi = 7.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 396 7 1 3 5.3 CCC(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
CHEMBL343028 237945 0 None None None Human 7.0 pKi = 7.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 396 7 1 3 5.3 CCC(C#N)(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccccc1 10.1021/jm990316l
44199443 335090 0 None None None Human 6.0 pKi = 6.0 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 378 6 2 3 4.0 CCC(NC(=O)C1CCCC1)C(O)C1CCN(c2ccc(Cl)cc2)CC1 nan
CHEMBL4449875 335090 0 None None None Human 6.0 pKi = 6.0 Binding
Displacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assayDisplacement of human [125I]-MIP-1alpha from CCR1 in human THP-1 cells incubated for 30 mins by radioligand binding assay
ChEMBL 378 6 2 3 4.0 CCC(NC(=O)C1CCCC1)C(O)C1CCN(c2ccc(Cl)cc2)CC1 nan
10810107 80381 0 None None None Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 384 6 2 4 4.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(O)cc1 10.1021/jm990316l
CHEMBL145106 80381 0 None None None Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 384 6 2 4 4.4 N#CC(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(O)cc1 10.1021/jm990316l
10572669 238197 0 None None None Human 7.0 pKi = 7.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 393 6 1 4 4.6 N#Cc1ccccc1C(C#N)CCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
CHEMBL344989 238197 0 None None None Human 7.0 pKi = 7.0 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 393 6 1 4 4.6 N#Cc1ccccc1C(C#N)CCCN1CCC(O)(c2ccc(Cl)cc2)CC1 10.1021/jm990316l
10576419 77690 0 None None None Human 7.0 pKi = 7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 472 9 1 3 6.7 N#CC(CCCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
CHEMBL142620 77690 0 None None None Human 7.0 pKi = 7 Binding
Inhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cellsInhibition of [125I]-MIP-1 alpha binding to recombinant human C-C chemokine receptor type 1 expressed in HEK293 cells
ChEMBL 472 9 1 3 6.7 N#CC(CCCCCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1 10.1021/jm990316l
44537841 1390 22 None None None Human 9.0 pIC50 = 9 Binding
Displacement of [<sup>125</sup>I]MIP-1&alpha; from CCR1 in human THP-1 cells.Displacement of [<sup>125</sup>I]MIP-1&alpha; from CCR1 in human THP-1 cells.
Guide to Pharmacology 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 25101488
57889181 1390 22 None None None Human 9.0 pIC50 = 9 Binding
Displacement of [<sup>125</sup>I]MIP-1&alpha; from CCR1 in human THP-1 cells.Displacement of [<sup>125</sup>I]MIP-1&alpha; from CCR1 in human THP-1 cells.
Guide to Pharmacology 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 25101488
9497 1390 22 None None None Human 9.0 pIC50 = 9 Binding
Displacement of [<sup>125</sup>I]MIP-1&alpha; from CCR1 in human THP-1 cells.Displacement of [<sup>125</sup>I]MIP-1&alpha; from CCR1 in human THP-1 cells.
Guide to Pharmacology 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 25101488
CHEMBL2398716 1390 22 None None None Human 9.0 pIC50 = 9 Binding
Displacement of [<sup>125</sup>I]MIP-1&alpha; from CCR1 in human THP-1 cells.Displacement of [<sup>125</sup>I]MIP-1&alpha; from CCR1 in human THP-1 cells.
Guide to Pharmacology 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 25101488
CHEMBL3334824 1390 22 None None None Human 9.0 pIC50 = 9 Binding
Displacement of [<sup>125</sup>I]MIP-1&alpha; from CCR1 in human THP-1 cells.Displacement of [<sup>125</sup>I]MIP-1&alpha; from CCR1 in human THP-1 cells.
Guide to Pharmacology 438 6 3 4 3.1 O=C(CC(O)(C)C)N[C@@H](C(=O)N1CC[C@](C(C1)(C)C)(O)c1ccc(cc1)Cl)C(C)C 25101488
3497 2447 26 None None None Human 8.0 pKd = 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 12909630
44309353 2447 26 None None None Human 8.0 pKd = 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 12909630
5311123 2447 26 None None None Human 8.0 pKd = 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 12909630
CHEMBL1628706 2447 26 None None None Human 8.0 pKd = 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 12909630
CHEMBL308473 2447 26 None None None Human 8.0 pKd = 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 482 11 4 6 2.5 O[C@H]([C@@H](NC(=O)c1cnc2c(n1)cccc2)Cc1cccc(c1)F)C[C@H](C(=O)N)CCC(O)(C)C 12909630
764 7613 0 None None None Human 8.2 pKd = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9336350
763 7611 0 None None None Human 8.4 pKd = 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7545673
763 7611 0 None None None Human 8.4 pKd = 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9115216
763 7611 0 None None None Human 8.4 pKd = 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9336350
765 7614 0 None None None Human 9.2 pKd = 9.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7545673
766 7615 0 None None None Human 8.3 pKd None 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9115216
762 7610 0 None None None Human 9.4 pKd None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9336350
2352 195309 69 None None None Human 8.1 pKi = 8.1 Binding
Binding affinity to CCR1Binding affinity to CCR1
Drug Central 444 6 3 9 0.9 Cc1nnc(C(=O)NC(C)(C)c2nc(C(=O)NCc3ccc(F)cc3)c(O)c(=O)n2C)o1 None
54671008 195309 69 None None None Human 8.1 pKi = 8.1 Binding
Binding affinity to CCR1Binding affinity to CCR1
Drug Central 444 6 3 9 0.9 Cc1nnc(C(=O)NC(C)(C)c2nc(C(=O)NCc3ccc(F)cc3)c(O)c(=O)n2C)o1 None
CHEMBL254316 195309 69 None None None Human 8.1 pKi = 8.1 Binding
Binding affinity to CCR1Binding affinity to CCR1
Drug Central 444 6 3 9 0.9 Cc1nnc(C(=O)NC(C)(C)c2nc(C(=O)NCc3ccc(F)cc3)c(O)c(=O)n2C)o1 None
DB06817 195309 69 None None None Human 8.1 pKi = 8.1 Binding
Binding affinity to CCR1Binding affinity to CCR1
Drug Central 444 6 3 9 0.9 Cc1nnc(C(=O)NC(C)(C)c2nc(C(=O)NCc3ccc(F)cc3)c(O)c(=O)n2C)o1 None
753 1716 0 None 1 2 Human 7.4 pKi = 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12381680
Q16627 1716 0 None 1 2 Human 7.4 pKi = 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12381680
757 1781 0 None -112 2 Human 7.5 pKi = 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12381680
757 1781 0 None -112 2 Human 7.5 pKi = 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8530354
P13236 1781 0 None -112 2 Human 7.5 pKi = 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12381680
P13236 1781 0 None -112 2 Human 7.5 pKi = 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8530354
758 1785 0 None -89 4 Human 7.5 pKi = 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8530354
758 1785 0 None -89 4 Human 7.5 pKi = 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9624164
P13501 1785 0 None -89 4 Human 7.5 pKi = 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8530354
P13501 1785 0 None -89 4 Human 7.5 pKi = 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9624164
759 1793 0 None -6 4 Human 8.1 pKi = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11994538
759 1793 0 None -6 4 Human 8.1 pKi = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12381680
P80098 1793 0 None -6 4 Human 8.1 pKi = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11994538
P80098 1793 0 None -6 4 Human 8.1 pKi = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12381680
512282 1562 44 None None None Human 8.6 pKi = 8.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10748002
767 1562 44 None None None Human 8.6 pKi = 8.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10748002
CHEMBL232656 1562 44 None None None Human 8.6 pKi = 8.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 434 6 2 4 3.1 NC(=O)Nc1cc(Cl)ccc1OCC(=O)N1CCN(C[C@H]1C)Cc1ccc(cc1)F 10748002
755 1754 0 None None None Human 8.9 pKi = 8.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12381680
P55773 1754 0 None None None Human 8.9 pKi = 8.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12381680
756 1775 0 None 3 2 Human 9.0 pKi = 9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11170631
756 1775 0 None 3 2 Human 9.0 pKi = 9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12381680
756 1775 0 None 3 2 Human 9.0 pKi = 9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8530354
756 1775 0 None 3 2 Human 9.0 pKi = 9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9624164
P10147 1775 0 None 3 2 Human 9.0 pKi = 9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11170631
P10147 1775 0 None 3 2 Human 9.0 pKi = 9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12381680
P10147 1775 0 None 3 2 Human 9.0 pKi = 9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8530354
P10147 1775 0 None 3 2 Human 9.0 pKi = 9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9624164
760 3401 0 None -3 2 Human 7.1 pKi None 7.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11170631
752 1464 0 None 12 2 Human 8.8 pKi None 8.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11170631