2,5-Disubstituted-1,3,4-oxadiazoles/thiadiazole as surface recognition moiety: Design and synthesis of novel hydroxamic acid based histone deacetylase inhibitors-Reference-Cited by-同舟云学术

2,5-Disubstituted-1,3,4-oxadiazoles/thiadiazole as surface recognition moiety: Design and synthesis of novel hydroxamic acid based histone deacetylase inhibitors

Published:2011-10 Issue:19 Volume:21 Page:5735-5738
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Rajak Harish,Agarawal Avantika,Parmar Poonam,Thakur Bhupendra Singh,Veerasamy Ravichandran,Sharma Prabodh Chander,Kharya Murli Dhar

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference26 articles.

1. Histone deacetylation in epigenetics: An attractive target for anticancer therapy

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

3. HDAC Inhibitors-New Generation of Target Specific Treatment

4. Histone deacetylases and cancer: causes and therapies

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