BDBM50429331 CHEMBL2334933

SMILES CS(=O)(=O)c1ccc(\C=C(\C(O)=O)c2ccc(Cl)cc2)cc1

InChI Key InChIKey=NABYNTJSTAGTSK-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 = 50429331   

TargetAldo-keto reductase family 1 member C2(Human)
University of Ljubljana

Curated by ChEMBL
LigandPNGBDBM50429331(CHEMBL2334933)
Affinity DataIC50: 2.69E+4nMAssay Description:Inhibition of recombinant AKR1C2 (unknown origin) assessed as decrease in oxidation of 1-acenaphthenol substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAldo-keto reductase family 1 member C1(Human)
University of Ljubljana

Curated by ChEMBL
LigandPNGBDBM50429331(CHEMBL2334933)
Affinity DataIC50: 1.57E+4nMAssay Description:Inhibition of human recombinant AKR1C1 expressed in Escherichia coli assessed as decrease in oxidation of 1-acenaphthenol substrate by spectrophotome...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAldo-keto reductase family 1 member C3(Human)
University of Ljubljana

Curated by ChEMBL
LigandPNGBDBM50429331(CHEMBL2334933)
Affinity DataIC50: 8.66E+4nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) assessed as decrease in oxidation of 1-acenaphthenol substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed