null

SMILES C[C@]12CC[C@H]3[C@@H](CC[C@H]4CC(=O)CCN34)[C@@H]1CCC2=O

InChI Key InChIKey=VWYXLVRVZRLBLR-YLVYSCNESA-N

  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 = 50057289   

Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50057289((5aS,7aS,10aS,10bS,12aS)-7a-Methyl-tetradecahydro-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory activity against 5-alpha Reductase-2 on human prostate homogenates from surgically derived benign hyperplastic tissueMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50057289((5aS,7aS,10aS,10bS,12aS)-7a-Methyl-tetradecahydro-...)copy SMILEScopy InChI
Affinity DataIC50: 2.90nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50057289((5aS,7aS,10aS,10bS,12aS)-7a-Methyl-tetradecahydro-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory activity against human 5-alpha Reductase-1 expressed in DU-145 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed