Conformational analogues of Oxamflatin as histone deacetylase inhibitors-Reference-Cited by-同舟云学术

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Conformational analogues of Oxamflatin as histone deacetylase inhibitors

Published:2006 Issue:20 Volume:4 Page:3778
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Dear Anthony E.,Liu Hong B.,Mayes Penelope A.,Perlmutter Patrick

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2006/OB/B608213K

Reference13 articles.

1. Histone Deacetylase Inhibitors: Inducers of Differentiation or Apoptosis of Transformed Cells

2. Oxamflatin is a novel antitumor compound that inhibits mammalian histone deacetylase

3. Histone Deacetylase Inhibitors

4. (2E)-5-[3-[(Phenylsulfonyl)amino]phenyl]- pent-2-en-4-ynohydroxamic Acid and Its Derivatives as Novel and Potent Inhibitors of ras Transformation

5. General method for the synthesis of trishydroxamic acids

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