Your browser doesn't support javascript.
loading
The Process and Strategy for Developing Selective Histone Deacetylase 3 Inhibitors.
Cao, Fangyuan; Zwinderman, Martijn R H; Dekker, Frank J.
Afiliação
  • Cao F; Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, 9713AV Groningen, The Netherlands. f.cao@rug.nl.
  • Zwinderman MRH; Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, 9713AV Groningen, The Netherlands. r.h.zwinderman@rug.nl.
  • Dekker FJ; Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, 9713AV Groningen, The Netherlands. f.j.dekker@rug.nl.
Molecules ; 23(3)2018 Mar 02.
Article em En | MEDLINE | ID: mdl-29498635
ABSTRACT
Histone deacetylases (HDACs) are epigenetic drug targets that have gained major scientific attention. Inhibition of these important regulatory enzymes is used to treat cancer, and has the potential to treat a host of other diseases. However, currently marketed HDAC inhibitors lack selectivity for the various HDAC isoenzymes. Several studies have shown that HDAC3, in particular, plays an important role in inflammation and degenerative neurological diseases, but the development of selective HDAC3 inhibitors has been challenging. This review provides an up-to-date overview of selective HDAC3 inhibitors, and aims to support the development of novel HDAC3 inhibitors in the future.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Desenho de Fármacos / Inibidores de Histona Desacetilases / Histona Desacetilases / Proteínas de Neoplasias / Neoplasias / Antineoplásicos Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Desenho de Fármacos / Inibidores de Histona Desacetilases / Histona Desacetilases / Proteínas de Neoplasias / Neoplasias / Antineoplásicos Idioma: En Ano de publicação: 2018 Tipo de documento: Article