Synthesis of new mono and bis amides projected as potential histone deacetylase (HDAC) inhibitors-Reference-Cited by-同舟云学术

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Synthesis of new mono and bis amides projected as potential histone deacetylase (HDAC) inhibitors

Published:2010-03 Issue:13 Volume:66 Page:2520-2528
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Terracciano Stefania,Chini Maria Giovanna,Bifulco Giuseppe,D'Amico Elisabetta,Marzocco Stefania,Riccio Raffaele,Bruno Ines

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference40 articles.

1. Epigenetic therapy of cancer: past, present and future

2. Epigenetics—An Epicenter of Gene Regulation: Histones and Histone-Modifying Enzymes

3. FR235222, a Fungal Metabolite, is a Novel Immunosuppressant that Inhibits Mammalian Histone Deacetylase. III. Structure Determination.

4. Biological Activities in Animal Models.

5. Taxonomy, Fermentation, Isolation and Biological Activities.

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2. Dual NAMPT/HDAC Inhibitors as a New Strategy for Multitargeting Antitumor Drug Discovery;ACS Medicinal Chemistry Letters;2017-12-19

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5. Can Small Chemical Modifications of Natural Pan-inhibitors Modulate the Biological Selectivity? The Case of Curcumin Prenylated Derivatives Acting as HDAC or mPGES-1 Inhibitors;Journal of Natural Products;2015-11-20

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