作者:Shinichiro Fuse、Kumiko Okada、Yusuke Iijima、Asami Munakata、Kazuhiro Machida、Takashi Takahashi、Motoki Takagi、Kazuo Shin-ya、Takayuki Doi
DOI:10.1039/c0ob01169j
日期:——
The total synthesis of a natural productHDAC inhibitor, spiruchostatin B, was successfully achieved. A 5-step synthesis that included an asymmetric aldol reaction was carried out in an automated synthesizer to provide an (E)-(S)-3-hydroxy-7-thio-4-heptenoic acid segment that is the crucial structure of cysteine-containing, depsipeptidic natural products such as spiruchostatins, FK228, FR901375, and largazole for their inhibitory activity against HDACs.
天然产物HDAC抑制剂spirochostatin B的全合成成功实现。通过自动化合成器执行了一种包含不对称羟醛反应的5步合成路线,得到了(E)-(S)-3-羟基-7-硫-4-庚烯酸片段,这一片段是包含半胱氨酸的脱硫肽类天然产物,如spirochostatins、FK228、FR901375和largazole,它们对HDACs具有抑制活性的关键结构。