null

SMILES OC(=O)\C=C\c1cc(OCc2ccccc2)cc(c1)C(=O)NCCc1ccccc1

InChI Key InChIKey=BMPXIXYIJSWPOS-VAWYXSNFSA-N

  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 2 hits for monomerid = 50509764   

TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
Texas Tech University Health Sciences Center

Curated by ChEMBL
LigandPNGBDBM50509764(CHEMBL4568995)copy SMILEScopy InChI
Affinity DataIC50: 160nMAssay Description:Inhibition of recombinant human AKR1C3 expressed in Escherichia coli BL21 (D3) using S-tetralol as substrate in presence of NADP+ by UV-spectrophotom...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8X52PubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
Texas Tech University Health Sciences Center

Curated by ChEMBL
LigandPNGBDBM50509764(CHEMBL4568995)copy SMILEScopy InChI
Affinity DataIC50: 2.60E+4nMAssay Description:Inhibition of recombinant human AKR1C2 expressed in Escherichia coli BL21 (D3) using S-tetralol as substrate in presence of NADP+ by UV-spectrophotom...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8X52PubMed