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Design, synthesis, and biological activity evaluation of a series of pleuromutilin derivatives with novel C14 side chains

机译:具有新型C14侧链的一系列胸膜霉素衍生物的设计,合成和生物活性评价

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摘要

In this work, according to the 'me-too me-better' design strategy, a peculiar side chain different from lefamulin at C14 position of pleuromutilin was introduced. A series of novel thioether pleuromutilin derivatives containing cyclohexane in the C14 chain was synthesized by ten-step synthesis reaction. All derivatives were characterized by Nuclear Magnetic Resonance (NMR) and High Resolution Mass Spectrometer (HRMS). Furthermore, majority of derivatives displayed moderate antibacterial activity in vitro. However, the compound 2C and 2J exhibited comparable or superior antibacterial activity to lefamulin. The summarized structure-activity relationship not only made the variety of pleuromutilin derivatives more diverse, but also provided new ideas for its design and development.
机译:在这项工作中,根据'ME-SOO-DEL-PERS-DELLY'的设计策略,引入了与胸脲素的C14位置不同的奇形侧链。 通过十步合成反应合成C14链中含有环己烷的一系列新型硫醚胸蛋白衍生物。 所有衍生物的特征在于核磁共振(NMR)和高分辨率质谱仪(HRMS)。 此外,大多数衍生物在体外显示中度抗菌活性。 然而,化合物2C和2J表现出与北甘油蛋白的相当或优异的抗菌活性。 总而言之的结构 - 活动关系不仅使得各种胸膜蛋白衍生物更加多样化,而且还为其设计和发展提供了新的思路。

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