Molecular Characterization and Bioactivity of Coumarin Derivatives from the Fruits of Cucumis bisexualis

被引:23
作者
Ma, Qin-Ge [1 ,2 ]
Wei, Rong-Rui [1 ]
Yang, Ming [1 ]
Huang, Xiao-Ying [1 ]
Wang, Fang [1 ]
Sang, Zhi-Pei [2 ]
Liu, Wen-Min [2 ]
Yu, Qing [2 ]
机构
[1] Jiangxi Univ Tradit Chinese Med, Res Ctr Nat Resources Chinese Med Mat & Ethn Med, Minist Educ,Key Lab Modern Preparat TCM, State Key Lab Innovat Drugs & High Efficiency Ene, Nanchang 330004, Jiangxi, Peoples R China
[2] Nanyang Normal Univ, Coll Chem & Pharmaceut Engn, Nanyang 473061, Peoples R China
基金
中国国家自然科学基金;
关键词
Cucumis bisexualis; coumarin derivative; anti-AChE; hepatoprotective; CONSTITUENTS; GLYCOSIDES; XANTHONES; GLABRA; BARK;
D O I
10.1021/acs.jafc.8b00976
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Cucumis bisexualis (Cucurbitaceae) is known as "mapao egg" or "muskmelon egg", which has been widely used as a wild melon in Chinese folk. Nine new coumarin derivatives (1-9), named 7-hydroxy-3-(4',6'-dihydroxy-5'-isopropyl-3 '',3 '' dimethyl-2H-chromen)-6-prenyl-2H-chromen-2-one (1), 7-hydroxy-3- (5 '-prenyl-3 '',3 ''-dim ethyl-2H-chromen )-6-prenyl-2H-chromen-2-one (2), 3-(6'-hydroxy-S'-prenyl-3 '',3 ''-dimethyl-2H-chromen)-6-prenyl-2H-chromen-2-one (3), 3-(5'-ethyl-3 '',3 '' dimethyl-2H-chromen)-6-prenyl-2H-chromen-2-one (4), 3-(4',6'-dihydroxy-S'-dimeth-ylallyl-3 '',3 ''-dimethyl-2H-chromen)-6-prenyl-2H-chromen-2-one (5), 344',6'-dihydroxy-5'-(2-pro-penyl)-3 '',3 ''-dimethyl-2H-chromenl-14,15-dimethyl-pyrano-chromen-2-one (6), 3-(6'-dihydroxy-5'-isopropanol-3 '',3 ''-dimethyl-2H-chromen)-14,15-dimethyl-pyrano-chromen-2-one (7), 3(5'-iso-pentenol-3 '',3 ''-dimethyl-2H-chromen)-14,15-dimethyl-pyrano-chromen-2-one (8), 3-(4',6'-dihydr-oxy-5'-prenyl-3 '',3 '' dimethyl-2H-chromen)-14,15-dimethyl-pyrano-chromen-2-one (9), together with 12 known compounds (10-21), were isolated and identified by spectroscopic analysis and references from the active site (EtOAc soluble fraction) of the fruits of C. bisexualis for the first time. Compounds (1-21) were evaluated for antiacetylcholinesterase (AChE) and hepatoprotective activities for the first time. Compounds 1, 3, 5, 6, 7, and 9 showed anti-AChE activities with IC50 values ranging from 11.23 to 89.69 mu M, and compounds 2, 4, 12, 15, 17, 18, and 19 (10 mu M) exhibited moderate hepatoprotective activities. These findings shed much light on a better understanding of the anti-AChE and hepatoprotective effects of these coumarin derivatives and provided new insights into developing better anti-AChE and hepatoprotective drugs in the future.
引用
收藏
页码:5540 / 5548
页数:9
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