| Literature DB >> 21874153 |
Daniel M Fass1, Rishita Shah, Balaram Ghosh, Krista Hennig, Stephanie Norton, Wen-Ning Zhao, Surya A Reis, Peter S Klein, Ralph Mazitschek, Rebecca L Maglathlin, Timothy A Lewis, Stephen J Haggarty.
Abstract
Carboxylic acids with known central nervous system and histone deacetylase (HDAC) inhibitory activities were converted to hydroxamic acids and tested using a suite of in vitro biochemical assays with recombinant HDAC isoforms, cell based assays in human cervical carcinoma Hela cells and primary cultures from mouse forebrain, and a whole animal (Xenopus laevis) developmental assay. Relative to the parent carboxylic acids, two of these analogs exhibited enhanced potency, and one analog showed altered HDAC isoform selectivity and in vivo activity in the Xenopus assay. We discuss potential uses of these novel hydroxamic acids in studies aimed at determining the utility of HDAC inhibitors as memory enhancers and mood stabilizers.Entities:
Year: 2010 PMID: 21874153 PMCID: PMC3161516 DOI: 10.1021/ml1001954
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345