BDBM3931 4-{3-[(1-phenyl-1H-1,3-benzodiazol-5-yl)oxy]propyl}morpholine::5-Substituted 1-Phenylbenzimidazole 20::5-[3-(4-Morpholino)propoxy]-1]phenylbenzimidazole Dihydrochloride

SMILES C(COc1ccc2n(cnc2c1)-c1ccccc1)CN1CCOCC1

InChI Key InChIKey=QPLWWFCARNPZGZ-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 = 3931   

TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
University of Auckland

LigandPNGBDBM3931(4-{3-[(1-phenyl-1H-1,3-benzodiazol-5-yl)oxy]propyl...)
Affinity DataIC50:  170nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
University of Auckland

LigandPNGBDBM3931(4-{3-[(1-phenyl-1H-1,3-benzodiazol-5-yl)oxy]propyl...)
Affinity DataIC50:  5.00E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
University of Auckland

LigandPNGBDBM3931(4-{3-[(1-phenyl-1H-1,3-benzodiazol-5-yl)oxy]propyl...)
Affinity DataIC50:  9.80E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed