BDBM42055 (E)-2-(1H-benzimidazol-2-yl)-3-(2-thienyl)acrylonitrile::(E)-2-(1H-benzimidazol-2-yl)-3-thiophen-2-yl-2-propenenitrile::(E)-2-(1H-benzimidazol-2-yl)-3-thiophen-2-yl-prop-2-enenitrile::(E)-2-(1H-benzimidazol-2-yl)-3-thiophen-2-ylprop-2-enenitrile::2-(1H-Benzoimidazol-2-yl)-3-thiophen-2-yl-acrylonitrile::MLS000567024::SMR000175048::cid_5334847

SMILES N#C\C(=C/c1cccs1)c1nc2ccccc2[nH]1

InChI Key InChIKey=MDVSLHGZTWHJMW-CSKARUKUSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 42055   

TargetBotulinum neurotoxin type A(Clostridium botulinum)
Microbiotix

Curated by ChEMBL
LigandPNGBDBM42055((E)-2-(1H-benzimidazol-2-yl)-3-(2-thienyl)acryloni...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Clostridium botulinum BoNT/A light chain-mediated SNAP-25 substrate cleavage after 40 mins by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Microbiotix

Curated by ChEMBL
LigandPNGBDBM42055((E)-2-(1H-benzimidazol-2-yl)-3-(2-thienyl)acryloni...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Bacillus anthracis lethal factor using MCA-KKVYPYPME[dnp]Kamide peptide substrate after 30 mins by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed