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TargetHistone deacetylase 2b
LigandBDBM50139944
Substrate/Competitorn/a
Meas. Tech.ChEMBL_87717 (CHEMBL857174)
IC50 145±n/a nM
Citation Mai, AMassa, SCerbara, IValente, SRagno, RBottoni, PScatena, RLoidl, PBrosch, G 3-(4-Aroyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamides as a new class of synthetic histone deacetylase inhibitors. 2. Effect of pyrrole-C2 and/or -C4 substitutions on biological activity. J Med Chem47:1098-109 (2004) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Histone deacetylase 2b
Name:Histone deacetylase 2b
Synonyms:Histone deacetylase HD2
Type:PROTEIN
Mol. Mass.:30785.07
Organism:Zea mays
Description:ChEMBL_87549
Residue:286
Sequence:
MEVGGQEVKPGATVSCKVGDGLVIHLSQAALGESKKASENAILSVNIDDKKLVLGTLSVE
KHPQISCDLVFDKDFELPHNSKTRSVFFRGYKSPVPLFESNSGEDSSDEELKTDQIPLQN
NEIKISAAKVPAKDDDDDVFIILAMMMMIYSSDDDDDDFTTSDSDNEMSEEDDSSDEDEM
SEEDDSSDEDEMSGGADPSDDSSDESGSEHTSAPKKTDVVVGKKRAIKAEAPYGKKAKSE
QSSQKTGDKASTSHPAKQSIKTPADKSRKTPTADKKSPKSGSHGCK
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50139944
n/a
NameBDBM50139944
Synonyms:CHEMBL12890 | N-Hydroxy-3-[1-methyl-4-(naphthalene-1-carbonyl)-1H-pyrrol-2-yl]-acrylamide
TypeSmall organic molecule
Emp. Form.C19H16N2O3
Mol. Mass.320.3419
SMILESCn1cc(cc1\C=C\C(=O)NO)C(=O)c1cccc2ccccc12
Structure
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