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The Total Synthesis and Biological Mode of Action of Largazole: A Potent Class I Histone Deacetylase (HDAC) Inhibitor

The efficient total synthesis of the recently described natural substance largazole (1) and it’s active metabolite largazole thiol (2) is described. The synthesis required eight linear steps and proceeded in 37% overall yield. It is demonstrated that largazole is a pro-drug, that is activated by rem...

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書誌詳細
主要な著者: Bowers, Albert, West, Nathan, Taunton, Jack, Schreiber, Stuart L., Bradner, James E., Williams, Robert M.
フォーマット: Artigo
言語:Inglês
出版事項: 2008
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3090445/
https://ncbi.nlm.nih.gov/pubmed/18642817
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ja8033763
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