BDBM50313668 CHEMBL1091082::N-(6-chloro-5-(4-fluorophenyl)-1H-indazol-3-yl)butyramide

SMILES CCCC(=O)Nc1n[nH]c2cc(Cl)c(cc12)-c1ccc(F)cc1

InChI Key InChIKey=NJIZXSCJRDEYGO-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 = 50313668   

TargetCytochrome P450 1A2(Homo sapiens (Human))
Sanofi-Aventis

Curated by ChEMBL
LigandPNGBDBM50313668(CHEMBL1091082 | N-(6-chloro-5-(4-fluorophenyl)-1H-...)
Affinity DataIC50:  830nMAssay Description:Inhibition of human recombinant CYP1A2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Sanofi-Aventis

Curated by ChEMBL
LigandPNGBDBM50313668(CHEMBL1091082 | N-(6-chloro-5-(4-fluorophenyl)-1H-...)
Affinity DataIC50:  22nMAssay Description:Inhibition of human recombinant GSK3-beta using gamma[33P]-ATP after 30 mins by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Sanofi-Aventis

Curated by ChEMBL
LigandPNGBDBM50313668(CHEMBL1091082 | N-(6-chloro-5-(4-fluorophenyl)-1H-...)
Affinity DataIC50:  130nMAssay Description:Inhibition of human recombinant GSK3beta by kinetic assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed