BDBM50407396 CHEMBL2112299

SMILES C[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O)CC[C@]34C)[C@@H]1CC=C2c1ccncc1

InChI Key InChIKey=MDKFLRXFVIMNBI-UHFFFAOYSA-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 = 50407396   

TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50407396(CHEMBL2112299)
Affinity DataIC50: 1.00E+3nMAssay Description:Ability to inhibit the C17,20-lyase enzyme by 50% using 17-alpha-hydroxyprogesterone as substrate.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Human)
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50407396(CHEMBL2112299)
Affinity DataIC50: 4.00E+3nMAssay Description:Ability to inhibit the Steroid 17-alpha-hydroxylase/17,20 lyase enzyme by 50%.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAromatase(Human)
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50407396(CHEMBL2112299)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Cytochrome P450 19A1More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed