BDBM50383528 CHEMBL2032251

SMILES ONC(=O)\C=C\c1ccccc1Cl

InChI Key InChIKey=HMGPSDPNANTYKH-AATRIKPKSA-N

Data  4 IC50

PDB links: 1 PDB ID matches this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50383528   

TargetBotulinum neurotoxin type A(Clostridium botulinum)
Fox Chase Chemical Diversity Center

Curated by ChEMBL
LigandPNGBDBM50383528(CHEMBL2032251)
Affinity DataIC50:  1.34E+4nMAssay Description:Inhibition of clostridium botulinum Botulinum neurotoxin type A using SNAPide as substrate by FRET analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 8(Homo sapiens (Human))TBA
LigandPNGBDBM50383528(CHEMBL2032251)
Affinity DataIC50:  54nMAssay Description:Inhibitory activity against recombinant Trypanosoma cruzi (Trypanosoma cruzi) Trypanothione reductaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50383528(CHEMBL2032251)
Affinity DataIC50:  100nMAssay Description:Inhibitory activity against recombinant Trypanosoma cruzi (Trypanosoma cruzi) Trypanothione reductaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetHistone deacetylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50383528(CHEMBL2032251)
Affinity DataIC50:  2.20E+3nMAssay Description:Inhibitory activity against recombinant Trypanosoma cruzi (Trypanosoma cruzi) Trypanothione reductaseMore data for this Ligand-Target Pair
In DepthDetails PubMed