AH6809


SMILES CC(Oc1ccc2c(c1)oc1c(c2=O)cc(cc1)C(=O)O)C
InChIKey AQFFXPQJLZFABJ-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 4
Hydrogen bond donors 1
Rotatable bonds 3
Molecular weight (Da) 298.1

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
DP1 PD2R Human Prostanoid A pKi 5.8 5.8 5.8 Guide to Pharmacology
EP1 PE2R1 Human Prostanoid A pKi 5.9 5.95 6.0 Guide to Pharmacology
EP2 PE2R2 Human Prostanoid A pKi 5.9 5.9 5.9 Guide to Pharmacology
EP3 PE2R3 Human Prostanoid A pKi 5.8 5.8 5.8 Guide to Pharmacology
EP1 PE2R1 Rat Prostanoid A pKi 5.9 5.9 5.9 Guide to Pharmacology
EP2 PE2R2 Rat Prostanoid A pKi 6.3 6.3 6.3 Guide to Pharmacology
EP2 PE2R2 Mouse Prostanoid A pKi 6.5 6.5 6.5 Guide to Pharmacology
EP2 PE2R2 Mouse Prostanoid A pKi 6.46 6.46 6.46 PDSP Ki database
EP4 PE2R4 Human Prostanoid A pKi 5.0 5.47 5.94 PDSP Ki database
EP3 PE2R3 Human Prostanoid A pKi 5.8 5.8 5.8 PDSP Ki database
FP PF2R Human Prostanoid A pKi 5.0 5.0 5.0 PDSP Ki database
EP2 PE2R2 Human Prostanoid A pKi 5.94 5.94 5.94 ChEMBL
DP1 PD2R Human Prostanoid A pKi 5.85 5.85 5.85 PDSP Ki database
DP1 PD2R Human Prostanoid A pKi 5.85 5.85 5.85 ChEMBL
EP1 PE2R1 Human Prostanoid A pKi 5.91 5.91 5.91 PDSP Ki database
EP1 PE2R1 Human Prostanoid A pKi 5.92 5.92 5.92 ChEMBL
EP3 PE2R3 Human Prostanoid A pKi 5.8 5.8 5.8 ChEMBL
IP PI2R Human Prostanoid A pKi 5.0 5.0 5.0 PDSP Ki database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database