Journal article

Antimalarial activity of the anticancer histone deacetylase inhibitor SB939

SDM Sumanadasa, CD Goodman, AJ Lucke, T Skinner-Adams, I Saham, A Haque, TA Do, GI McFadden, DP Fairlie, KT Andrews

Antimicrobial Agents and Chemotherapy | Published : 2012

Abstract

Histone deacetylase (HDAC) enzymes posttranslationally modify lysines on histone and nonhistone proteins and play crucial roles in epigenetic regulation and other important cellular processes. HDAC inhibitors (e.g., suberoylanilide hydroxamic acid [SAHA; also known as vorinostat]) are used clinically to treat some cancers and are under investigation for use against many other diseases. Development of new HDAC inhibitors for noncancer indications has the potential to be accelerated by piggy-backing onto cancer studies, as several HDAC inhibitors have undergone or are undergoing clinical trials. One such compound, SB939, is a new orally active hydroxamate-based HDAC inhibitor with an improved ..

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