ginkgolide C


SMILES O=C1O[C@@H]2[C@@]([C@@H]1C)(O)[C@@]13C4(C2O)[C@H](OC3=O)[C@@H]([C@H](C24[C@H](O1)OC(=O)C2O)C(C)(C)C)O
InChIKey AMOGMTLMADGEOQ-WXQWCWKOSA-N

Chemical properties

Hydrogen bond acceptors 11
Hydrogen bond donors 4
Rotatable bonds 0
Molecular weight (Da) 440.1

Drug properties

Molecular type Small molecule
Endogenous/Surrogate Surrogate
Approved drug No

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
FFA1 FFAR1 Human Free fatty acid A pKi 6.66 6.66 6.66 ChEMBL
EP3 PE2R3 Human Prostanoid A pKi 6.4 6.4 6.4 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
FFA1 FFAR1 Human Free fatty acid A pEC50 7.3 7.3 7.3 Guide to Pharmacology
FFA4 FFAR4 Human Free fatty acid A pEC50 5.46 5.46 5.46 Guide to Pharmacology
FFA1 FFAR1 Rat Free fatty acid A pEC50 7.0 7.0 7.0 ChEMBL
FFA4 FFAR4 Human Free fatty acid A pEC50 5.46 5.6 5.85 ChEMBL
FFA1 FFAR1 Human Free fatty acid A pEC50 4.75 6.87 7.89 ChEMBL