Synthesis and biological evaluation of histone deacetylase inhibitors that are based on FR235222: A cyclic tetrapeptide scaffold-Reference-Cited by-同舟云学术

Synthesis and biological evaluation of histone deacetylase inhibitors that are based on FR235222: A cyclic tetrapeptide scaffold

Published:2008-04 Issue:8 Volume:18 Page:2549-2554
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Singh Erinprit K.,Ravula Suchitra,Pan Chung-Mao,Pan Po-Shen,Vasko Robert C.,Lapera Stephanie A.,Weerasinghe Sujith V.W.,Pflum Mary Kay H.,McAlpine Shelli R.

Publisher

Elsevier BV

Subject

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

Reference23 articles.

1. Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer

2. Histone Deacetylase Inhibitors

3. Histone-deacetylase inhibitors: novel drugs for the treatment of cancer

4. HDAC inhibitors: Clinical update and mechanism-based potential

5. Trichostatin A, an inhibitor of histone deacetylases, strongly suppresses growth of pancreatic adenocarcinoma cells

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