BDBM50093598 17-(2-Hydroxyimino-propyl)-10,13-dimethyl-1,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-2H-cyclopenta[a]phenanthrene-3,6-dione::CHEMBL136097

SMILES CC(CC1CCC2C3CC(=O)C4=CC(=O)CCC4(C)C3CCC12C)N=O

InChI Key InChIKey=MBSYQDOIFSFBSL-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50093598   

Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
University Of The Saarland

Curated by ChEMBL
LigandPNGBDBM50093598(17-(2-Hydroxyimino-propyl)-10,13-dimethyl-1,7,8,9,...)
Affinity DataIC50:  430nMAssay Description:Evaluated for the inhibitory activity against human steroid 5-alpha-reductase type 2 from human BPH tissue at 210 nM of testosteroneMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of The Saarland

Curated by ChEMBL
LigandPNGBDBM50093598(17-(2-Hydroxyimino-propyl)-10,13-dimethyl-1,7,8,9,...)
Affinity DataIC50:  2.90E+3nMAssay Description:Inhibition of Human steroid 5-alpha-reductase type I expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
University Of The Saarland

Curated by ChEMBL
LigandPNGBDBM50093598(17-(2-Hydroxyimino-propyl)-10,13-dimethyl-1,7,8,9,...)
Affinity DataIC50:  860nMAssay Description:Inhibition of Human steroid 5-alpha-reductase type II expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of The Saarland

Curated by ChEMBL
LigandPNGBDBM50093598(17-(2-Hydroxyimino-propyl)-10,13-dimethyl-1,7,8,9,...)
Affinity DataIC50:  900nMAssay Description:Evaluated for the inhibitory activity against human steroid 5-alpha-reductase type I in human DU-145 cell assay at 5 nM of androstenedioneMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed