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A novel HDAC inhibitor with a hydroxy-pyrimidine scaffold. Bioorganic & medicinal chemistry letters, 2011/07/15, Volume 21, Issue 14, p.4164-9, (2011)
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Chemical genetic strategy identifies histone deacetylase 1 (HDAC1) and HDAC2 as therapeutic targets in sickle cell disease. Proceedings of the National Academy of Sciences of the United States of America, 2010/07/13, Volume 107, Issue 28, p.12617-22, (2010)
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Chemical phylogenetics of histone deacetylases. Nature chemical biology, 2010/03/01, Volume 6, Issue 3, p.238-243, (2010)
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Synthesis and histone deacetylase inhibitory activity of largazole analogs: alteration of the zinc-binding domain and macrocyclic scaffold. Organic letters, 2009/03/19, Volume 11, Issue 6, p.1301-4, (2009)
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Synthesis and conformation-activity relationships of the peptide isosteres of FK228 and largazole. Journal of the American Chemical Society, 2009/03/04, Volume 131, Issue 8, p.2900-5, (2009)
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Total synthesis and biological mode of action of largazole: a potent class I histone deacetylase inhibitor. Journal of the American Chemical Society, 2008/08/20, Volume 130, Issue 33, p.11219-22, (2008)
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