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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >1,3,4-Oxadiazoline derivatives as novel potential inhibitors targeting chitin biosynthesis: design, synthesis and biological evaluation.
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1,3,4-Oxadiazoline derivatives as novel potential inhibitors targeting chitin biosynthesis: design, synthesis and biological evaluation.

机译:1,3,4-氧代唑啉衍生物作为新型潜在抑制剂靶向甲壳素生物合成:设计,合成和生物学评价。

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摘要

Two series of 1,3,4-oxadiazoline heterocycle derivatives were designed, synthesized and identified. Bioactivity assays showed that all synthesized compounds inhibited chitin synthesis in yeast, suggesting they might be a novel class of potential inhibitors against chitin biosynthesis. The structure-activity relationships (SAR) of these compounds are discussed.
机译:设计,合成和鉴定了两种1,3,4-氧代唑杂环杂环衍生物。 生物活性测定表明,所有合成的化合物抑制了酵母中的依甲酸甲酸甲酸甲酸丝蛋白合成,表明它们可能是对依托丁蛋白生物合成的新类潜在的抑制剂。 讨论了这些化合物的结构 - 活性关系(SAR)。

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