查尔酮
萜烯
酚类
化学
微生物
萜类
传统医学
药用植物
抗菌剂
生物化学
生物
细菌
立体化学
有机化学
医学
遗传学
作者
Changxuan Deng,Nan Zhang,Hanlin Lin,Wangting Lu,Fei Ding,Yangguang Gao,Yongmin Zhang
标识
DOI:10.2174/0109298673272908231115101520
摘要
α-Glucosidase inhibitors (AGIs) showcase versatile biochemical activities with respect to antidiabetic, anticancerous, antiobese and antiviral effects. They have drawn a great deal of attention from the scientific community. While α-glucosidase inhibitors are mostly discovered from plants and microorganisms, the recent advance in natural α- glucosidase inhibitors over the past five years has been reviewed in this article, and 139 distinct α-glucosidase inhibitors from the plants and microorganisms were classified into ten groups based on their chemical structures, including flavonoids (34), xanthones (6), alkaloids (8), benzopyrones / benzofuranones (8), terpenes (25), saponins (6), phenols / alcohols (25), esters (20), chalcone (5) and other compounds (2). In this review, we mainly focused on the novel chemical structures and the various biological activities of theses natural AGIs. Some of the selected natural compounds exhibit powerful α-glucosidase inhibitory activity and anti-tumor activity, may hold promise to become the candidate drugs for treating type II diabetes and cancer in future.
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