BDBM50150336 (4R,6S)-4-Hydroxy-6-({[4-((8S,11R,13S,14S,17S)-17-hydroxy-13-methyl-3-oxo-17-prop-1-ynyl-2,3,6,7,8,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-11-yl)-phenyl]-methyl-amino}-methyl)-tetrahydro-pyran-2-one::CHEMBL182961

SMILES CC#C[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@H](C[C@]12C)c1ccc(cc1)N(C)C[C@@H]1C[C@@H](O)CC(=O)O1

InChI Key InChIKey=AEMCKZFBFDARJV-WRFREBFJSA-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 = 50150336   

TargetGlucocorticoid receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50150336((4R,6S)-4-Hydroxy-6-({[4-((8S,11R,13S,14S,17S)-17-...)
Affinity DataIC50:  140nMAssay Description:Inhibition of dexamethasone-induced glucocorticoid receptor mediated tyrosine aminotransferase in rat hepatocytesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50150336((4R,6S)-4-Hydroxy-6-({[4-((8S,11R,13S,14S,17S)-17-...)
Affinity DataIC50:  2.30nMAssay Description:Inhibition of [3H]dexamethasone binding to human glucocorticoid receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProgesterone receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50150336((4R,6S)-4-Hydroxy-6-({[4-((8S,11R,13S,14S,17S)-17-...)
Affinity DataIC50:  3.80nMAssay Description:Inhibition of human progesterone receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50150336((4R,6S)-4-Hydroxy-6-({[4-((8S,11R,13S,14S,17S)-17-...)
Affinity DataIC50:  23nMAssay Description:Inhibition of dexamethasone-induced glucocorticoid receptor mediated alkaline phosphatase activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed