BDBM26041 2-chloro-5-(2-phenyl-5-(pyridin-4-yl)-1H-imidazol-4-yl)phenol::2-chloro-5-[2-phenyl-5-(pyridin-4-yl)-1H-imidazol-4-yl]phenol::CHEMBL373011::L-779,450::L-779450

SMILES Oc1cc(ccc1Cl)-c1[nH]c(nc1-c1ccncc1)-c1ccccc1

InChI Key InChIKey=WXJLXRNWMLWVFB-UHFFFAOYSA-N

Data  2 IC50  2 Kd

  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 4 hits for monomerid = 26041   

TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Gsk

LigandPNGBDBM26041(2-chloro-5-(2-phenyl-5-(pyridin-4-yl)-1H-imidazol-...)
Affinity DataKd:  2.40nMpH: 7.5 T: 2°CAssay Description:The kinase enzyme, fluorescent ligand and a variable concentration of test compound are incubated together to reach thermodynamic equilibrium under c...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM26041(2-chloro-5-(2-phenyl-5-(pyridin-4-yl)-1H-imidazol-...)
Affinity DataIC50:  1.40nMAssay Description:Inhibition of Raf1 kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Gsk

LigandPNGBDBM26041(2-chloro-5-(2-phenyl-5-(pyridin-4-yl)-1H-imidazol-...)
Affinity DataIC50:  10nMAssay Description:Inhibition bRaf kinase activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Gsk

LigandPNGBDBM26041(2-chloro-5-(2-phenyl-5-(pyridin-4-yl)-1H-imidazol-...)
Affinity DataKd:  2.40nMAssay Description:Binding affinity at bRaf kinase in fluorescent ligand displacement assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed