cholic acid


SMILES O[C@@H]1CC[C@]2([C@@H](C1)C[C@H]([C@@H]1[C@@H]2C[C@H](O)[C@]2([C@H]1CC[C@@H]2[C@@H](CCC(=O)O)C)C)O)C
InChIKey BHQCQFFYRZLCQQ-OELDTZBJSA-N

Chemical properties

Hydrogen bond acceptors 4
Hydrogen bond donors 4
Rotatable bonds 4
Molecular weight (Da) 408.3

Drug properties

Molecular type Small molecule
Physiological/Surrogate Endogenous
Approved drug Yes

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
GPBA GPBAR Human Bile acid A pEC50 4.7 4.84 4.87 ChEMBL
GPBA GPBAR Human Bile acid A pIC50 5.22 5.22 5.22 ChEMBL
GPBA GPBAR Human Bile acid A pEC50 8.3 8.3 8.3 Drug Central
GPBA GPBAR Human Bile acid A pEC50 5.0 5.0 5.0 Guide to Pharmacology
GPBA GPBAR Mouse Bile acid A pIC50 5.28 5.28 5.28 ChEMBL