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N-Hydroxy-(4-oxime)-cinnamide: A versatile scaffold for the synthesis of novel histone deacetilase (HDAC) inhibitors

By Giannini G, Marzi M, Pezzi R, Brunetti T, Battistuzzi G, Di Marzo M, Cabri W, Vesci L and Pisano C

Abstract

With the aim to discover novel HDAC inhibitors with high potency and good safety profiles, we have designed a small library based on a N-hydroxy-(4-oxime)-cinnamide scaffold. We describe the synthesis of these novel compounds and some preliminary in vitro cytotoxic activity on three tumor cell lines, NB4, H460 and HCT116, as well as their inhibitory activity against class I, II and IV HDAC. Several 4-oxime derivatives demonstrated a promising inhibitory activity on HDAC6 and HDAC8 coupled to a good selectivity profile. (C) 2009 Elsevier Ltd. All rights reserved

Topics: HDAC, cancer
Publisher: 'Elsevier BV'
Year: 2009
DOI identifier: 10.1016/j.bmcl.2009.02.029
OAI identifier: oai:cris.unibo.it:11585/756754
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