BDBM50366722 CHEMBL1793827

SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2cn(OC)c3ccccc23)NC(=O)[C@H](CCCCCC(O)=O)NC(=O)[C@H]2CCCCN2CC1=O

InChI Key InChIKey=SIVWRIUCOPXNRQ-RPKRYSFNSA-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 = 50366722   

TargetHistone deacetylase(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50366722(CHEMBL1793827)
Affinity DataIC50:  15nMAssay 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
LigandPNGBDBM50366722(CHEMBL1793827)
Affinity DataIC50:  30nMAssay 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