BDBM50366969 CHEMBL1790593

SMILES CC[C@@H](C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OC)cc2)NC(=O)[C@H](CCCCCCC(=O)NO)NC(=O)[C@H]2CCCCN2C1=O

InChI Key InChIKey=IDNMSLGHIWCDPW-UHFFFAOYSA-N

Data  1 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50366969   

TargetHistone deacetylase(Cryptosporidium parvum)
Institute of Technology

Curated by ChEMBL
LigandPNGBDBM50366969(CHEMBL1790593)
Affinity DataIC50: 4.80nMAssay Description:Inhibitory activity against histone deacetylases (HDAC) prepared from mouse melanoma B16/BL6 cells; Not testedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed