BDBM50174543 (3R,5R,10R,13S)-3-Hydroxy-10,13-dimethyl-tetradecahydro-cyclopenta[a]phenanthrene-4,17-dione::CHEMBL198818
SMILES: C[C@]12CCC3C(CC[C@H]4C(=O)[C@H](O)CC[C@]34C)C1CCC2=O
InChI Key: InChIKey=UXTAKINVUOEXAI-OZTGMACGSA-N
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cytochrome P450 19A1 (Homo sapiens (Human)) | BDBM50174543![]() ((3R,5R,10R,13S)-3-Hydroxy-10,13-dimethyl-tetradeca...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 147 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Oporto Curated by ChEMBL | Assay Description Inhibition constant against aromatase protein from human placental microsomes using [1-beta-3H]-androstenedione; Competitive inhibition | J Med Chem 48: 6379-85 (2005) Article DOI: 10.1021/jm050129p BindingDB Entry DOI: 10.7270/Q25M66GD | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 19A1 (Homo sapiens (Human)) | BDBM50174543![]() ((3R,5R,10R,13S)-3-Hydroxy-10,13-dimethyl-tetradeca...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 670 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Oporto Curated by ChEMBL | Assay Description Inhibitory concentration against aromatase protein from human placental microsomes using [1-beta-3H]-androstenedione; Competitive inhibition | J Med Chem 48: 6379-85 (2005) Article DOI: 10.1021/jm050129p BindingDB Entry DOI: 10.7270/Q25M66GD | |||||||||||
More data for this Ligand-Target Pair |