galanin(3-29) (rat/mouse)


SMILES CC[C@H](C)[C@H](NC(=O)[C@H](C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)CNC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)[C@@H](C)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)O)[C@@H](C)O
InChIKey OEYNEKWXIPNQHZ-VFYYSKAESA-N
Sequence TLNSAGYLLGPHAIDNHRSFSDKHGLT

Chemical properties

Hydrogen bond acceptors 43
Hydrogen bond donors 43
Rotatable bonds 93
Molecular weight (Da) 2920.5

Drug properties

Molecular type Peptide
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
GAL1 GALR1 Rat Galanin A pKi 6.0 6.0 6.0 Guide to Pharmacology
GAL2 GALR2 Mouse Galanin A pKi 5.66 5.66 5.66 Guide to Pharmacology
GAL1 GALR1 Mouse Galanin A pKi 5.78 5.78 5.78 Guide to Pharmacology
GAL3 GALR3 Rat Galanin A pKi 6.0 6.0 6.0 Guide to Pharmacology
GAL2 GALR2 Rat Galanin A pKi 5.51 5.75 6.0 Guide to Pharmacology
GAL2 GALR2 Human Galanin A pKi 6.15 6.15 6.15 Guide to Pharmacology
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
GAL1 GALR1 Rat Galanin A pIC50 6.0 6.0 6.0 Guide to Pharmacology
GAL1 GALR1 Human Galanin A pIC50 6.0 6.0 6.0 Guide to Pharmacology
GAL2 GALR2 Rat Galanin A pIC50 6.0 6.0 6.0 Guide to Pharmacology