化学
黄荆
类黄酮
IC50型
立体化学
牡荆
二维核磁共振波谱
有机化学
传统医学
抗氧化剂
体外
生物化学
医学
作者
Ngoc‐Hong Nguyen,Thuc‐Huy Duong,Huy Truong Nguyen,Y. Thien Vu,Thi‐Minh‐Dinh Tran,Thi‐Thanh‐Van Ho,Chi‐Cong Mai,Dinh‐Tri Mai,Hoang‐Chuong Nguyen,Huong Thuy Le,Duc‐Dung Pham
标识
DOI:10.1002/cbdv.202300390
摘要
Adenosma bracteosum and Vitex negundo are natural sources of methoxylated flavonoids. Little is known about the α-glucosidase inhibition of multi-methoxylated flavonoid derivatives. Eighteen natural flavonoids were isolated from A. bracteosum and V. negundo. Seven halogenated derivatives were synthesized. Their chemical structures were elucidated by extensive NMR analysis and high-resolution mass spectroscopy as well as comparisons in literature. All compounds were evaluated for their α-glucosidase inhibition. Most compounds showed good activity with IC50 values ranging from 16.7 to 421.8 μM. 6,8-Dibromocatechin was the most active compound with an IC50 value of 16.7 μM. A molecular docking study was conducted, indicating that those compounds are potent α-glucosidase inhibitors.
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