首页> 外文期刊>European journal of organic chemistry >Synthesis of (4R,12S,15S,16S,19R,20R,34S)-Muricatetrocin and (4R,12S,15S,16S,19R,20R,34S)-Muricatertrocin,Two Potent Inhibitors of Mitochondrial Complex I
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Synthesis of (4R,12S,15S,16S,19R,20R,34S)-Muricatetrocin and (4R,12S,15S,16S,19R,20R,34S)-Muricatertrocin,Two Potent Inhibitors of Mitochondrial Complex I

机译:(4R,12S,15S,16S,19R,20R,34S)-Muricatetrocin和(4R,12S,15S,16S,19R,20R,34S)-Muricatertrocin的两种线粒体复合物强抑制剂I的合成

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摘要

(4R,12S,15S,16S,19R,20R,34S)-Muricatetrocin (1) and (4R,12S,15S,16S,19R,20R,34S)-muricatetrocin (2) were synthesized by a modular synthetic strategy. Both compounds act as potent inhibitors of mitochondrial complex I. Compound 1 showed analtical data in a greement with howiicin E and a fit with the date for muricatetrocin A if one reassigns the reported ~(13)C signals for C(13) and C(14). Compound 2 matched muricatetrocin B in respect to all NMR data. However,a lower optical rotation was found for 2 ([#alpha#]_D~(28)=+6.7) than was reprted for the natural product ([#alpha#]_D~(25)=+15.0).
机译:(4R,12S,15S,16S,19R,20R,34S)-Muricatetrocin(1)和(4R,12S,15S,16S,19R,20R,34S)-Muricatetrocin(2)通过模块化合成策略合成。两种化合物均是线粒体复合体I的有效抑制剂。如果一个化合物重新分配了报道的C(13)和C(〜)的〜(13)C信号,则化合物1在与how霉素E的关系中显示出分析数据,并与鼠毛霉素A的日期相吻合。 14)。就所有NMR数据而言,化合物2匹配鼠毛霉素B。但是,发现2([#alpha#] _ D〜(28)= + 6.7)的旋光度比天然产物([#alpha#] _ D〜(25)= + 15.0)低。

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