BDBM27723 3-(4-methoxyphenyl)quinoxaline-5-carboxamide::CHEMBL519443::quinoxaline analogue, 3e

SMILES COc1ccc(cc1)-c1cnc2cccc(C(N)=O)c2n1

InChI Key InChIKey=XLKSSLKAULIQEE-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 = 27723   

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

LigandPNGBDBM27723(3-(4-methoxyphenyl)quinoxaline-5-carboxamide | CHE...)
Affinity DataIC50:  71nMpH: 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

LigandPNGBDBM27723(3-(4-methoxyphenyl)quinoxaline-5-carboxamide | CHE...)
Affinity DataIC50:  71nMAssay 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

LigandPNGBDBM27723(3-(4-methoxyphenyl)quinoxaline-5-carboxamide | CHE...)
Affinity DataIC50:  8nMT: 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