Back to Search
Start Over
Histone deacetylase activators: N-acetylthioureas serve as highly potent and isozyme selective activators for human histone deacetylase-8 on a fluorescent substrate.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2011 Oct 01; Vol. 21 (19), pp. 5920-3. Date of Electronic Publication: 2011 Aug 04. - Publication Year :
- 2011
-
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.<br /> (Copyright © 2011 Elsevier Ltd. All rights reserved.)
- Subjects :
- 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
Benzamides chemical synthesis
Benzamides pharmacology
Enzyme Activators chemical synthesis
Enzyme Activators pharmacology
Histone Deacetylases metabolism
Phenylthiourea analogs & derivatives
Software
Thiourea analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3405
- Volume :
- 21
- Issue :
- 19
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 21865040
- Full Text :
- https://doi.org/10.1016/j.bmcl.2011.07.080