BDBM50078834 2-(pyridin-2-yl)-1H-benzo[d]imidazole::2-pyridin-2-yl-1H-benzoimidazole::CHEMBL72683

SMILES c1ccc(nc1)-c1nc2ccccc2[nH]1

InChI Key InChIKey=YNFBMDWHEHETJW-UHFFFAOYSA-N

Data  4 IC50  1 Kd  1 EC50

  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 6 hits for monomerid = 50078834   

TargetSerine/threonine-protein kinase mTOR(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50078834(2-(pyridin-2-yl)-1H-benzo[d]imidazole | 2-pyridin-...)
Affinity DataKd:  6.00E+4nMAssay Description:Dissociation constant when binding to FK506 binding protein (FKBP).More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetMethionine aminopeptidase(Escherichia coli (strain K12))
Saarland University

Curated by ChEMBL
LigandPNGBDBM50078834(2-(pyridin-2-yl)-1H-benzo[d]imidazole | 2-pyridin-...)
Affinity DataIC50: 574nMAssay Description:Inhibition of Co2+ loaded MetAP expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCytochrome P450 2B1(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50078834(2-(pyridin-2-yl)-1H-benzo[d]imidazole | 2-pyridin-...)
Affinity DataIC50: 6.46E+4nMAssay Description:Inhibitory potency to aminopyrine N-demethylase activity (P450) in hepatic microsomes from phenobarbitone-induced rats.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetMethionine aminopeptidase 1(Human)
Universit£T Heidelberg

Curated by ChEMBL
LigandPNGBDBM50078834(2-(pyridin-2-yl)-1H-benzo[d]imidazole | 2-pyridin-...)
Affinity DataIC50: 2.84E+4nMAssay Description:Inhibition of human MetAP1More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetMethionine aminopeptidase 2(Human)
Universit£T Heidelberg

Curated by ChEMBL
LigandPNGBDBM50078834(2-(pyridin-2-yl)-1H-benzo[d]imidazole | 2-pyridin-...)
Affinity DataIC50: 1.33E+4nMAssay Description:Inhibition of human MetAP2 expressed in baculovirus infected Sf9 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetFocal adhesion kinase 1(Human)
Goethe University Frankfurt

Curated by ChEMBL
LigandPNGBDBM50078834(2-(pyridin-2-yl)-1H-benzo[d]imidazole | 2-pyridin-...)
Affinity DataEC50:  1.03E+5nMAssay Description:Inhibition of N-terminal NanoLuc-tagged full length FAK (unknown origin) transfected in HEK293T cells pre-incubated with compound for 2 hrs followed ...More data for this Ligand-Target Pair
In DepthDetails
PubMed