null

SMILES [H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C(=O)C(O)=C(C[C@]12C)C#N

InChI Key InChIKey=WNPBBBQFDAPUSS-KJXREMBBSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50123013   

TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50123013(CHEMBL3623216)copy SMILEScopy InChI
Affinity DataIC50: 1.02E+3nMAssay Description:Inhibition of human placental microsomal aromatase using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release preincubated for 5...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7D2SPubMed
TargetAromatase(Homo sapiens (Human))
State University of New York Upstate Medical University

Curated by ChEMBL
LigandPNGBDBM50123013(CHEMBL3623216)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC84Q6PubMed