Discovery of Potent and Selective Histone Deacetylase Inhibitors via Focused Combinatorial Libraries of Cyclic α3β-Tetrapeptides-Reference-Cited by-同舟云学术

Discovery of Potent and Selective Histone Deacetylase Inhibitors via Focused Combinatorial Libraries of Cyclic α3β-Tetrapeptides

Published:2009-08-25 Issue:23 Volume:52 Page:7836-7846
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Olsen Christian A.¹,Ghadiri M. Reza¹

Affiliation:

1. Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm900850t

Reference90 articles.

1. Chromatin Modifications and Their Function

2. New Nomenclature for Chromatin-Modifying Enzymes

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

4. Class II histone deacetylases: versatile regulators

5. Stat3 Dimerization Regulated by Reversible Acetylation of a Single Lysine Residue

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