SKF-38393


SMILES Oc1cc2CCNCC(c2cc1O)c1ccccc1
InChIKey JUDKOGFHZYMDMF-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 3
Hydrogen bond donors 3
Rotatable bonds 1
Molecular weight (Da) 255.1

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Ligand site mutations D1 D2 D5

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
D1 DRD1 Human Dopamine A pKi 6.2 6.5 6.8 Guide to Pharmacology
D5 DRD5 Human Dopamine A pKi 7.0 7.0 7.0 Guide to Pharmacology
D5 DRD5 Human Dopamine A pKi 6.61 7.36 9.3 ChEMBL
D1 DRD1 Rat Dopamine A pKi 7.19 7.24 7.46 ChEMBL
α2C ADA2C Human Adrenoceptors A pKi 7.08 7.08 7.08 ChEMBL
D2 DRD2 Rat Dopamine A pKd 4.34 4.5 4.75 ChEMBL
D2 DRD2 Rat Dopamine A pKi 5.16 5.24 5.54 ChEMBL
D1 DRD1 Human Dopamine A pKi 6.41 7.34 9.0 ChEMBL
D1 DRD1 Human Dopamine A pKd 6.82 6.82 6.82 ChEMBL
D2 DRD2 Human Dopamine A pKi 5.02 5.48 6.8 ChEMBL
D2 DRD2 Human Dopamine A pKd 5.02 5.02 5.02 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
D1 DRD1 Goldfish Dopamine A pEC50 6.02 6.02 6.02 ChEMBL
D1 DRD1 Rat Dopamine A pIC50 4.97 6.61 7.46 ChEMBL
D1 DRD1 Rat Dopamine A pEC50 7.0 7.0 7.0 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 4.5 4.62 4.75 ChEMBL
α2C ADA2C Human Adrenoceptors A pEC50 5.86 5.86 5.86 ChEMBL
D2 DRD2 Rat Dopamine A pIC50 5.43 5.43 5.43 ChEMBL
D1 DRD1 Human Dopamine A pEC50 6.18 6.92 8.96 ChEMBL