BDBM27722 3-[4-(trifluoromethyl)phenyl]quinoxaline-5-carboxamide::CHEMBL521428::quinoxaline analogue, 3d

SMILES NC(=O)c1cccc2ncc(nc12)-c1ccc(cc1)C(F)(F)F

InChI Key InChIKey=TVFZZQMNVBEMRP-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 = 27722   

TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Fujisawa Pharmaceutical

LigandPNGBDBM27722(3-[4-(trifluoromethyl)phenyl]quinoxaline-5-carboxa...)
Affinity DataIC50:  118nMpH: 8.0 T: 2°CAssay Description:To assess the inhibitory activity of novel inhibitors, the PARP enzyme assay was carried out in reaction mixture consisting of activated salmon teste...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Fujisawa Pharmaceutical

LigandPNGBDBM27722(3-[4-(trifluoromethyl)phenyl]quinoxaline-5-carboxa...)
Affinity DataIC50:  118nMAssay Description:Inhibition of human recombinant PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 2(Mus musculus (Mouse))
Fujisawa Pharmaceutical

LigandPNGBDBM27722(3-[4-(trifluoromethyl)phenyl]quinoxaline-5-carboxa...)
Affinity DataIC50:  11nMT: 2°CAssay Description:To assess the inhibitory activity of novel inhibitors, the PARP enzyme assay was carried out in reaction mixture consisting of activated salmon teste...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed