BDBM50340426 16-Dehydropregnenolone acetate::CHEMBL1761683

SMILES CC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@@]4(C)[C@@H](CC=C4C(C)=O)[C@@H]3CC=C2C1

InChI Key InChIKey=MZWRIOUCMXPLKV-RFOVXIPZSA-N

Data  3 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 3 hits for monomerid = 50340426   

TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50340426(16-Dehydropregnenolone acetate | CHEMBL1761683)
Affinity DataIC50:  1.71E+3nMAssay Description:Inhibition of human testicular 17-alpha-hydroxylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50340426(16-Dehydropregnenolone acetate | CHEMBL1761683)
Affinity DataIC50:  1.89E+3nMAssay Description:Inhibition of human testicular steroid 17-alpha-hydroxylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50340426(16-Dehydropregnenolone acetate | CHEMBL1761683)
Affinity DataIC50:  3.56E+4nMAssay Description:Inhibition of human DPP-4 assessed as cleavage of substrate using H-Gly-Pro-AMC chromogenic substrate after 10 mins by double beam spectrophotometerMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed