BDBM50067250 (E)-N-({[3-(3-Bromo-2-methyl-imidazo[1,2-a]pyridin-8-yloxymethyl)-2,4-dichloro-phenyl]-methyl-carbamoyl}-methyl)-3-(4-methanesulfonylamino-phenyl)-acrylamide; hydrochloride::CHEMBL538281

SMILES CN(C(=O)CNC(=O)\C=C\c1ccc(NS(C)(=O)=O)cc1)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl

InChI Key InChIKey=ADUFOLJVECWGCS-MDWZMJQESA-N

Data  2 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 2 hits for monomerid = 50067250   

TargetB2 bradykinin receptor(Homo sapiens (Human))
Fujisawa Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067250((E)-N-({[3-(3-Bromo-2-methyl-imidazo[1,2-a]pyridin...)
Affinity DataIC50:  4.80nMAssay Description:Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoidcarcinoma) which express Bradykinin receptor B...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetB2 bradykinin receptor(Cavia porcellus)
Fujisawa Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067250((E)-N-({[3-(3-Bromo-2-methyl-imidazo[1,2-a]pyridin...)
Affinity DataIC50:  3.90nMAssay Description:Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed