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Bioorg Med Chem Lett ; 21(19): 5920-3, 2011 Oct 01.
Article in English | MEDLINE | ID: mdl-21865040

ABSTRACT

We report, for the first time, that certain N-acetylthiourea derivatives serve as highly potent and isozyme selective activators for the recombinant form of human histone deacetylase-8 in the assay system containing Fluor-de-Lys as a fluorescent substrate. The experimental data reveals that such activating feature is manifested via decrease in the K(m) value of the enzyme's substrate and increase in the catalytic turnover rate of the enzyme.


Subject(s)
Benzamides/chemical synthesis , Benzamides/pharmacology , Enzyme Activators/chemical synthesis , Enzyme Activators/pharmacology , Histone Deacetylases/metabolism , Phenylthiourea/analogs & derivatives , Software , Thiourea/analogs & derivatives , Benzamides/chemistry , Binding Sites , Dose-Response Relationship, Drug , Drug Design , Drug Discovery , Enzyme Activation , Enzyme Activators/chemistry , Fluorescent Dyes/metabolism , Humans , Isoenzymes/metabolism , Kinetics , Models, Chemical , Molecular Targeted Therapy , Phenylthiourea/chemical synthesis , Phenylthiourea/chemistry , Phenylthiourea/pharmacology , Structure-Activity Relationship , Substrate Specificity , Thiourea/chemistry
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