null

SMILES [H][C@@]12C[C@H](C#N)[C@H](O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CCC2=C(Sc3ccccc3)C(=O)CC[C@]12C

InChI Key InChIKey=GPIRVQGMLLEUJS-WDYHNDBASA-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 2 hits for monomerid = 50123012   

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

Curated by ChEMBL
LigandPNGBDBM50123012(CHEMBL3623217)copy SMILEScopy InChI
Affinity DataIC50: 169nMAssay Description:Inhibition of human placental microsomal aromatase using [1beta-3H] androstenedione as substrate assessed as tritiated H2O release after 5 mins by be...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
LigandPNGBDBM50123012(CHEMBL3623217)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC84Q6PubMed