| Literature DB >> 20637529 |
Paola Conti1, Lucia Tamborini, Andrea Pinto, Laura Sola, Roberta Ettari, Ciro Mercurio, Carlo De Micheli.
Abstract
A series of isoxazole-based histone deacetylase (HDAC) inhibitors structurally related to SAHA were designed and synthesized. The isoxazole moiety was inserted in the vicinity of the Zn(2+)-binding group in order to check its participation in the coordinating process. 2010 Elsevier Masson SAS. All rights reserved.Entities:
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Year: 2010 PMID: 20637529 DOI: 10.1016/j.ejmech.2010.06.035
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514