BDBM16590 2-(1H-indazol-3-yl)-1H-1,3-benzodiazole::3-(1H-benzimidazol-2-yl)-1H-indazole::CHEMBL383990::Indazole Compound 2

SMILES c1ccc2[nH]c(nc2c1)-c1n[nH]c2ccccc12

InChI Key InChIKey=JTKFRFMSUBOCIQ-UHFFFAOYSA-N

Data  1 KI  11 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 12 hits for monomerid = 16590   

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM16590(2-(1H-indazol-3-yl)-1H-1,3-benzodiazole | CHEMBL38...)
Affinity DataIC50: 6.30E+3nMpH: 7.5 T: 2°CAssay Description:Kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor compound in the presence ATP/[gamma-33P] ATP. 33P ...More data for this Ligand-Target Pair
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LigandPNGBDBM16590(2-(1H-indazol-3-yl)-1H-1,3-benzodiazole | CHEMBL38...)
Affinity DataIC50: 845nMpH: 7.5 T: 2°CAssay Description:Kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor compound in the presence ATP/[gamma-33P] ATP. 33P ...More data for this Ligand-Target Pair
In DepthDetails Article
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TargetCyclin-A2/Cyclin-dependent kinase 2(Human)
Vernalis (R&D)

LigandPNGBDBM16590(2-(1H-indazol-3-yl)-1H-1,3-benzodiazole | CHEMBL38...)
Affinity DataIC50: 1.43E+4nMpH: 7.5 T: 2°CAssay Description:Kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor compound in the presence ATP/[gamma-33P] ATP. 33P ...More data for this Ligand-Target Pair
In DepthDetails Article
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TargetGlycogen synthase kinase-3 beta(Human)
Vernalis (R&D)

LigandPNGBDBM16590(2-(1H-indazol-3-yl)-1H-1,3-benzodiazole | CHEMBL38...)
Affinity DataIC50: 744nMpH: 7.5 T: 2°CAssay Description:Kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor compound in the presence ATP/[gamma-33P] ATP. 33P ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM16590(2-(1H-indazol-3-yl)-1H-1,3-benzodiazole | CHEMBL38...)
Affinity DataIC50: 2.71E+3nMpH: 7.5 T: 2°CAssay Description:Kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor compound in the presence ATP/[gamma-33P] ATP. 33P ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM16590(2-(1H-indazol-3-yl)-1H-1,3-benzodiazole | CHEMBL38...)
Affinity DataIC50: 5.00E+4nMpH: 7.5 T: 2°CAssay Description:Kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor compound in the presence ATP/[gamma-33P] ATP. 33P ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM16590(2-(1H-indazol-3-yl)-1H-1,3-benzodiazole | CHEMBL38...)
Affinity DataIC50: 2.00E+5nMpH: 7.5 T: 2°CAssay Description:Kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor compound in the presence ATP/[gamma-33P] ATP. 33P ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM16590(2-(1H-indazol-3-yl)-1H-1,3-benzodiazole | CHEMBL38...)
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM16590(2-(1H-indazol-3-yl)-1H-1,3-benzodiazole | CHEMBL38...)
Affinity DataIC50: 720nMAssay Description:Inhibition of VEGFR1More data for this Ligand-Target Pair
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PubMed
TargetFibroblast growth factor receptor 1(Human)
Chiron

Curated by ChEMBL
LigandPNGBDBM16590(2-(1H-indazol-3-yl)-1H-1,3-benzodiazole | CHEMBL38...)
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of FGFR1More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM16590(2-(1H-indazol-3-yl)-1H-1,3-benzodiazole | CHEMBL38...)
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibition of VEGFR2More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM16590(2-(1H-indazol-3-yl)-1H-1,3-benzodiazole | CHEMBL38...)
Affinity DataKi:  8.58E+3nM ΔG°:  -7.02kcal/molepH: 7.5 T: 2°CAssay Description:For Ki determinations a matrix of inhibitor and substrate concentrations were tested. Inhibitor concentrations were tested from four times IC50 with ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed