BDBM50366743 CHEMBL1793968

SMILES CC[C@H](C)c1[nH]c(=O)c(CC(O)c2ccccc2[N+]([O-])=O)nc(O)c(CCCCCC(=O)CC)[nH]c(O)c2CCCCn2c1O

InChI Key InChIKey=RGCSYUOQCDTHCU-VGCIPCNWSA-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 = 50366743   

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

Curated by ChEMBL
LigandPNGBDBM50366743(CHEMBL1793968)
Affinity DataIC50:  91nMAssay Description:Inhibitory activity against histone deacetylase (HDAC) enzyme derived from partially purified extracts of human HeLa cells using [3H]11 as radioligan...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Cryptosporidium parvum)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50366743(CHEMBL1793968)
Affinity DataIC50:  33nMAssay Description:Inhibitory activity against histone deacetylase enzyme derived from partially purified extracts of Eimeria tenella protozoa using [3H]11 as radioliga...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed