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Chemical Phylogenetics of Histone Deacetylases

The broad study of histone deacetylases in chemistry, biology and medicine relies on tool compounds to derive mechanistic insights. A phylogenetic analysis of Class I and II HDACs as targets of a comprehensive, structurally diverse panel of inhibitors revealed unexpected isoform selectivity even amo...

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Detalles Bibliográficos
Autores principales: Bradner, James E., West, Nathan, Grachan, Melissa L., Greenberg, Edward F., Haggarty, Stephen J., Warnow, Tandy, Mazitschek, Ralph
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822059/
https://www.ncbi.nlm.nih.gov/pubmed/20139990
http://dx.doi.org/10.1038/nchembio.313
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author Bradner, James E.
West, Nathan
Grachan, Melissa L.
Greenberg, Edward F.
Haggarty, Stephen J.
Warnow, Tandy
Mazitschek, Ralph
author_facet Bradner, James E.
West, Nathan
Grachan, Melissa L.
Greenberg, Edward F.
Haggarty, Stephen J.
Warnow, Tandy
Mazitschek, Ralph
author_sort Bradner, James E.
collection PubMed
description The broad study of histone deacetylases in chemistry, biology and medicine relies on tool compounds to derive mechanistic insights. A phylogenetic analysis of Class I and II HDACs as targets of a comprehensive, structurally diverse panel of inhibitors revealed unexpected isoform selectivity even among compounds widely perceived as non-selective. The synthesis and study of a focused library of cinnamic hydroxamates allowed the identification of a first non-selective HDAC inhibitor. These data will guide a more informed use of HDAC inhibitors as chemical probes and therapeutic agents.
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spelling pubmed-28220592010-09-01 Chemical Phylogenetics of Histone Deacetylases Bradner, James E. West, Nathan Grachan, Melissa L. Greenberg, Edward F. Haggarty, Stephen J. Warnow, Tandy Mazitschek, Ralph Nat Chem Biol Article The broad study of histone deacetylases in chemistry, biology and medicine relies on tool compounds to derive mechanistic insights. A phylogenetic analysis of Class I and II HDACs as targets of a comprehensive, structurally diverse panel of inhibitors revealed unexpected isoform selectivity even among compounds widely perceived as non-selective. The synthesis and study of a focused library of cinnamic hydroxamates allowed the identification of a first non-selective HDAC inhibitor. These data will guide a more informed use of HDAC inhibitors as chemical probes and therapeutic agents. 2010-02-07 2010-03 /pmc/articles/PMC2822059/ /pubmed/20139990 http://dx.doi.org/10.1038/nchembio.313 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Bradner, James E.
West, Nathan
Grachan, Melissa L.
Greenberg, Edward F.
Haggarty, Stephen J.
Warnow, Tandy
Mazitschek, Ralph
Chemical Phylogenetics of Histone Deacetylases
title Chemical Phylogenetics of Histone Deacetylases
title_full Chemical Phylogenetics of Histone Deacetylases
title_fullStr Chemical Phylogenetics of Histone Deacetylases
title_full_unstemmed Chemical Phylogenetics of Histone Deacetylases
title_short Chemical Phylogenetics of Histone Deacetylases
title_sort chemical phylogenetics of histone deacetylases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822059/
https://www.ncbi.nlm.nih.gov/pubmed/20139990
http://dx.doi.org/10.1038/nchembio.313
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