星形毒素:合成与生物学研究

E. El-Sawy, G. Kirsch, Mohamed Abdel-Aziz
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引用次数: 1

摘要

Asteltoxins属于一组多烯吡咯真菌毒素,已知是线粒体ATP合成和ATP水解的有效抑制剂。Asteltoxin A首次从玉米毒曲霉(Aspergillus stellatus)中分离得到。已经进行了几次尝试来合成星毒素A,从合成双(四氢呋喃)片段开始,这在以前的生物合成研究中得到了证明。本文综述了星藻毒素的真菌来源、类似星藻毒素的生物合成途径、合成试验及其生物活性。这是第一次对1979年至2023年期间进行审查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Asteltoxins: Synthesis and Biological Studies
Asteltoxins belong to a group of polyene pyrone mycotoxins that are known to be potent inhibitors of mitochondrial ATP synthesis and ATP hydrolysis. Asteltoxin A was first isolated from the toxic maize cultures of Aspergillus stellatus. Several attempts have been made to synthesize asteltoxin A, starting with the synthesis of a bis(tetrahydrofuran) moiety that has been demonstrated previously in biosynthetic studies. This review highlights the fungal sources of asteltoxins, similar asteltoxins, biosynthetic pathways, their synthetic trials, and their biological activities. This review is the first of its kind covering the periods from 1979 to 2023.
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