Xanthine oxidase inhibitory constituents from the roots of Ampelopsis japonica

被引:0
作者
Li, Yu-Lin [1 ,2 ,3 ]
Liu, Fen [1 ,2 ,3 ,4 ]
Zhao, Li-Yun [1 ,2 ,3 ]
Li, Han-Xiang [1 ,2 ,3 ]
Jumai, Aikebaier [1 ,2 ,3 ]
Xu, Zhi-Fang [1 ,2 ,3 ]
Qiu, Sheng-Xiang [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, State Key Lab Plant Divers & Specialty Crops, Guangzhou, Peoples R China
[2] Chinese Acad Sci, Guangdong Prov Key Lab Appl Bot, South China Bot Garden, Guangzhou, Peoples R China
[3] South China Natl Bot Garden, Guangzhou, Peoples R China
[4] Univ Chinese Acad Sci, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Ampelopsis japonica; bioactive compounds; ampejaponoside a and B; xanthine oxidase activity; molecular docking; TRITERPENE GLYCOSIDES; SAPONINS; DOCKING;
D O I
10.1080/14786419.2024.2341308
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Bioassay-guided purification of the xanthine oxidase (XOD) inhibitory extract of the roots of Ampelopsis japonica resulted in the isolation of two new triterpenoids (1-2), designated Ampejaponoside A and B, along with sixteen known compounds (3-18). The structures of Ampejaposide A and B were elucidated by comprehensive analysis of spectroscopic data with the structures of the known compounds 3-18 confirmed by comparison the spectral data with corresponding values reported in literatures. All the isolates were evaluated for their XOD inhibitory activity in vitro. As a result, compounds 2, 8, and 14-16 displayed significant XOD inhibitory effect, particularly 16 being the most potent with an IC50 value of 0.21 mu M, superior to positive substance allopurinol (IC50 1.95 mu M). Molecular docking uncovered a unique interaction mode of 16 with the active site of XOD. The current study showed that the triterpenoids and polyphenols from A. japonica could serve as new lead compounds with the potential to speed up the development of novel XOD inhibitors with clinical potential to treat hyperuricaemia and gout. [GRAPHICS]
引用
收藏
页数:10
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