Five glycosylated phenolic derivatives from the bark of Ilex rotunda Thunb. and their anti-inflammatory activities

被引:1
作者
Peng, Shou [1 ,2 ]
Chen, Tong [1 ]
Wang, Ge [1 ,2 ]
Li, Chen-yue [1 ,2 ]
Liu, Wen-jing [3 ]
Wang, Wen-qiong [1 ]
Xuan, Li-jiang [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Medica, State Key Lab Drug Res, Shanghai, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Chinese Mat Med, Nanjing, Peoples R China
关键词
Ilex rotunda; hemiterpene glycosides; phenolic glycosides; anti-inflammatory activity; INFLAMMATORY MEDIATORS; KERATINOCYTES; CONSTITUENTS; GLYCOSIDES; AKT;
D O I
10.1080/14786419.2022.2078323
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Five new glycosylated phenolic derivatives, rotundosides A-E (1-5), and three known glycosides (6-8) were isolated from the 95% alcohol extract of the bark of Ilex rotunda. Their structures were elucidated by extensive spectroscopic analysis and comparison with the literature data. All new compounds possessed a [5-O-(E)-caffeoyl]-beta-D-apiofuranosyl-(1 -> 6)-beta-D-glucopyranosyl group. The anti-inflammatory properties of all isolated compounds were evaluated using a modified nitric oxide (NO) production in lipopolysaccharide (LPS)-induced leukemia cells in mouse macrophage (RAW264.7) method. Compound 8, dracunculifoside H, showed significant anti-inflammatory activity in vitro.
引用
收藏
页码:571 / 578
页数:8
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