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首页> 外文期刊>Proceedings of the Japan Academy, Series B. Physical and Biological Sciences >Recent development of two chitinase inhibitors, Argifin and Argadin, produced by soil microorganisms
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Recent development of two chitinase inhibitors, Argifin and Argadin, produced by soil microorganisms

机译:由土壤微生物产生的两种几丁质酶抑制剂Argifin和Argadin的最新开发

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摘要

Chitin, the second most abundant polysaccharide in nature, occurs in fungi; some algae and many invertebrates, including insects. Thus, chitin synthesis and degradation could represent specific targets for fungicides and insecticides. Chitinases hydrolyze chitin into oligomers of N-acetyl-D-glucosamine at key points in the life cycles of organisms, consequently, chitinase inhibitors have become subject of increasing interest. This review covers the development of two chitinase inhibitors of natural origin, Argifin and Argadin, isolated from the cultured broth of microorganisms in our laboratory. In particular, the practical total synthesis of these natural products, the synthesis of lead compounds via, computer-aided rational molecular design, and discovery methods that generate only highly-active compounds using a kinetic target (chitinase)guided synthesis approach (termed in situ click chemistry) are described.
机译:几丁质是自然界中第二丰富的多糖,存在于真菌中。一些藻类和许多无脊椎动物,包括昆虫。因此,几丁质的合成和降解可能代表杀菌剂和杀虫剂的特定目标。几丁质酶在生物体生命周期的关键点将几丁质水解为N-乙酰基-D-葡萄糖胺的低聚物,因此,几丁质酶抑制剂已成为人们越来越感兴趣的主题。这篇综述涵盖了从我们实验室的微生物培养液中分离得到的两种自然来源的几丁质酶抑制剂Argifin和Argadin的开发。特别是这些天然产物的实际总合成,通过计算机辅助的合理分子设计合成先导化合物以及使用动力学靶标(几丁质酶)指导的合成方法(原位合成)仅生成高活性化合物的发现方法点击化学)进行说明。

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