BDBM50105688 (E)-N-Hydroxy-3-[4-(3-trifluoromethyl-benzenesulfonylamino)-phenyl]-acrylamide::CHEMBL95195::N-hydroxy-3-(4-(3-(trifluoromethyl)phenylsulfonamido)phenyl)acrylamide::US8796330, 114

SMILES ONC(=O)\C=C\c1ccc(NS(=O)(=O)c2cccc(c2)C(F)(F)F)cc1

InChI Key InChIKey=PDIYZRMQLKPNAP-RMKNXTFCSA-N

Data  3 IC50  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50105688   

TargetHistone deacetylase 1(Homo sapiens (Human))
Methylgene

US Patent
LigandPNGBDBM50105688((E)-N-Hydroxy-3-[4-(3-trifluoromethyl-benzenesulfo...)
Affinity DataIC50:  100nMT: 2°CAssay Description:For deacetylase assays, 20,000 cpm of the [3H]-metabolically labeled acetylated histone substrate (M. Yoshida et al., J. Biol. Chem. 265(28): 17174-1...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetHistone deacetylase 8(Homo sapiens (Human))TBA
LigandPNGBDBM50105688((E)-N-Hydroxy-3-[4-(3-trifluoromethyl-benzenesulfo...)
Affinity DataIC50:  100nMAssay Description:Inhibition of Homo sapiens (human) HDAC8More data for this Ligand-Target Pair
In DepthDetails Article
TargetHistone deacetylase 1(Homo sapiens (Human))
Methylgene

US Patent
LigandPNGBDBM50105688((E)-N-Hydroxy-3-[4-(3-trifluoromethyl-benzenesulfo...)
Affinity DataEC50:  2.20E+4nMAssay Description:Concentration of compound required for acetylation of histone-4 in human T24 cancer cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Methylgene

US Patent
LigandPNGBDBM50105688((E)-N-Hydroxy-3-[4-(3-trifluoromethyl-benzenesulfo...)
Affinity DataIC50:  100nMAssay Description:In vitro inhibition of partially purified recombinant human Histone deacetylase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed