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TargetHistone deacetylase 11
LigandBDBM587635
Substrate/Competitorn/a
Meas. Tech.In Vitro Histone Deacetylase Assay I
IC50<500±n/a nM
Citation Zheng, XMartin, MWNg, PYThomason, JRHan, BRudnitskaya, ALancia, Jr., DR Isoindolines as HDAC inhibitors US Patent US11535607 Publication Date 12/27/2022
More Info.:Get all data from this article,  Assay Method
 
Histone deacetylase 11
Name:Histone deacetylase 11
Synonyms:HD11 | HDA11_HUMAN | HDAC11 | Human HDAC11
Type:Chromatin regulator; hydrolase; repressor
Mol. Mass.:39187.66
Organism:Homo sapiens (Human)
Description:Q96DB2
Residue:347
Sequence:
MLHTTQLYQHVPETRWPIVYSPRYNITFMGLEKLHPFDAGKWGKVINFLKEEKLLSDSML
VEAREASEEDLLVVHTRRYLNELKWSFAVATITEIPPVIFLPNFLVQRKVLRPLRTQTGG
TIMAGKLAVERGWAINVGGGFHHCSSDRGGGFCAYADITLAIKFLFERVEGISRATIIDL
DAHQGNGHERDFMDDKRVYIMDVYNRHIYPGDRFAKQAIRRKVELEWGTEDDEYLDKVER
NIKKSLQEHLPDVVVYNAGTDILEGDRLGGLSISPAGIVKRDELVFRMVRGRRVPILMVT
SGGYQKRTARIIADSILNLFGLGLIGPESPSVSAQNSDTPLLPPAVP
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM587635
n/a
NameBDBM587635
Synonyms:(R)-N-hydroxy-3,3-dimethyl-2-(5- (trifluoromethyl)pyrazin-2-yl)indoline- 7-carboxamide | US11535607, Example 40-3
TypeSmall organic molecule
Emp. Form.C16H15F3N4O2
Mol. Mass.352.3111
SMILESCC1(C)[C@@H](Nc2c1cccc2C(=O)NO)c1cnc(cn1)C(F)(F)F |r|
Structure
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