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抗霉素A结构改造的研究进展 被引量:4

Research Progress in Structural Modification of Antimycin A
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摘要 抗霉素A(Antimycin A)是一类具有大环双内酯结构的天然产物,是典型的线粒体呼吸链细胞色素bc_1复合物Q_i位点抑制剂.鉴于该类化合物的独特结构与超高活性,越来越多的科研工作者对其展开了系统深入的研究.本文主要总结了Antimycin A的发现、生物活性研究,及近年来科研工作者对其进行结构改造所取得的成果. Antimycin A is a class of natural products bearing a dilactone-ring moiety as the core skeleton. These compounds have been identified as specific inhibitors of the mitochondrial respiratory chain and bind to the Q_i site of the cytochrome bc_1 complex. Due to its unique structure and extremly high activity, it has aroused great interest of researchers. The development and biological activities of antimycin A are mainly described, and the recent results of its structural modifications are summarized.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2017年第6期1368-1381,共14页 Chinese Journal of Organic Chemistry
基金 国家自然科学基金(Nos.21472063 21502062) 湖北省教育厅一般项目(No.Q20102606) 襄阳市科技局一般项目(No.2010GG1B33) 低维光电材料与器件湖北省重点实验室(No.HLOM151005)资助项目~~
关键词 抗霉素A 抑制剂 生物活性 结构改造 antimycin A inhibitor biological activity structural modification
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