BDBM50031674 (3S,10R,13S,17R)-10,13-Dimethyl-17-pyridin-4-yl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol::CHEMBL310690

SMILES C[C@]12CCC3C(CC=C4C[C@@H](O)CC[C@]34C)C1CC[C@@H]2c1ccncc1

InChI Key InChIKey=XAAZZZPPMNDFEH-GOVWGFSTSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50031674   

TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50031674((3S,10R,13S,17R)-10,13-Dimethyl-17-pyridin-4-yl-2,...)
Affinity DataIC50:  160nMAssay Description:Ability to inhibit the Steroid 17-alpha-hydroxylase/17,20 lyase enzyme by 50%.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50031674((3S,10R,13S,17R)-10,13-Dimethyl-17-pyridin-4-yl-2,...)
Affinity DataIC50:  160nMAssay Description:Inhibition of human progesterone 17-alpha-hydroxylase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50031674((3S,10R,13S,17R)-10,13-Dimethyl-17-pyridin-4-yl-2,...)
Affinity DataIC50:  53nMAssay Description:Ability to inhibit the C17,20-lyase enzyme by 50% using 17-alpha-hydroxyprogesterone as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed