BDBM50546234 CHEMBL4758386

SMILES OC(=O)c1cccc(Nc2ccc([N+]([O-])=O)c3c(cccc23)[N+]([O-])=O)c1

InChI Key InChIKey=DEBLYSMOATYNAJ-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50546234   

TargetAldo-keto reductase family 1 member C4(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50546234(CHEMBL4758386)
Affinity DataIC50: 5.34E+3nMAssay Description:Inhibition of human AKR1C4 using S-tetralol as substrate in presence of NADP by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAldo-keto reductase family 1 member C2(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50546234(CHEMBL4758386)
Affinity DataIC50: 1.56E+4nMAssay Description:Inhibition of human AKR1C2 using S-tetralol as substrate in presence of NADP by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAldo-keto reductase family 1 member C3(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50546234(CHEMBL4758386)
Affinity DataIC50: 53nMAssay Description:Inhibition of human AKR1C3 using S-tetralol as substrate in presence of NADP by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAldo-keto reductase family 1 member C1(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50546234(CHEMBL4758386)
Affinity DataIC50: 1.54E+4nMAssay Description:Inhibition of human AKR1C1 using S-tetralol as substrate in presence of NADP by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed