CYPROTERONE ACETATE


SMILES CC(=O)O[C@]1(C(C)=O)CC[C@H]2[C@@H]3C=C(Cl)C4=CC(=O)[C@@H]5C[C@@H]5[C@]4(C)[C@H]3CC[C@@]21C
InChIKey UWFYSQMTEOIJJG-FDTZYFLXSA-N

Chemical properties

Hydrogen bond acceptors 4
Hydrogen bond donors 0
Rotatable bonds 2
Molecular weight (Da) 416.2

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
A1 AA1R Rat Adenosine A pKi 8.89 9.0 9.12 ChEMBL
μ OPRM Human Opioid A pKi 6.05 6.05 6.05 ChEMBL
μ OPRM Human Opioid A pKi 8.22 8.22 8.22 Drug Central
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
A1 AA1R Rat Adenosine A pIC50 6.9 7.6 8.3 ChEMBL
μ OPRM Human Opioid A pIC50 5.66 5.66 5.66 ChEMBL
TSH TSHR Human Glycoprotein hormone A Potency 4.4 4.4 4.4 ChEMBL
A1 AA1R Rat Adenosine A pIC50 8.08 8.08 8.08 Drug Central