阿维菌素的研究进展:基于阿维菌素结构衍生化的综述

Lili Dong , Jianjun Zhang
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引用次数: 4

摘要

阿维菌素是一种从阿维菌链霉菌中分离出来的发酵衍生的大环内酯,作为生物制药在农业、医学和兽医领域有着悠久的历史。由于具有显著的生物活性和低的哺乳动物毒性,阿维菌素已被公认为最具市场竞争力的驱虫药和杀虫剂之一,与这些化合物相关的研究已被授予2015年诺贝尔生理学或医学奖。阿维菌素分子中含有碳碳双键、羟基和夹竹桃等多个反应位点,通过化学修饰可以进一步开发出具有更好的理化性质、生物利用度、害虫谱和药效的衍生物。目前,已有数千种阿维菌素衍生物被研究,许多品种已被商业化用于作物保护和制药用途。本文综述了阿维菌素结构修饰反应的研究进展,并对其构效关系作了进一步总结。这篇综述可能为未来开发高效的阿维菌素类驱虫药、杀菌剂和杀虫剂提供重要的见解。
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Research progress of avermectin: A minireview based on the structural derivatization of avermectin

Avermectins, a fermentation-derived macrocyclic lactones isolated from Streptomyces avermitilis, exhibiting a long history as biopharmaceuticals used in agriculture, medical and veterinary fields. Due to the significant biological activity and low mammalian toxicity, avermectins have been recognized as one of the most market-competitive anthelmintics and insecticides, with research related to these compounds has been awarded the 2015 Nobel Prize in Physiology or Medicine. Avermectin molecules contain multiple reaction sites, such as carbon-carbon double bonds, hydroxyl groups and oleandrose, facilitating the further development of derivatives with improved physicochemical properties, bioavailability, pest spectrum, and efficacy by chemical modification. Presently, thousands of avermectin derivatives have been studied and various species have been commercialized for crop protection and pharmaceutical use. Herein, we review the research progress achieved on structural modification reactions of avermectin and further summarize their structure-activity relationships. This mini-review may provide important insights into the future development of efficient avermectin-based anthelmintics, fungicides, and insecticides.

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