BDBM50366698 CHEMBL1793944

SMILES CCC(CCCCC[C@@H]1NC(=O)[C@H]2CCCCN2CC(=O)[C@@H](NC(=O)[C@H](Cc2cn(OC)c3ccccc23)NC1=O)[C@@H](C)CC)SC(C)=O

InChI Key InChIKey=ZMLFRAJSAWUTBS-JMUZYZKLSA-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 = 50366698   

TargetHistone deacetylase(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50366698(CHEMBL1793944)
Affinity DataIC50:  73nMAssay Description:Inhibitory activity against histone deacetylase (HDAC) derived from partially purified extracts of human HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Cryptosporidium parvum)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50366698(CHEMBL1793944)
Affinity DataIC50:  110nMAssay Description:Inhibitory activity against histone deacetylase (HDAC) from partially purified extracts of Eimeria tenella protozoal cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed