Synthesis of coumarin derivatives and their cytoprotective effects on t-BHP-induced oxidative damage in HepG2 cells

被引:16
|
作者
Ando, Tomomi [1 ]
Nagumo, Mina [2 ]
Ninomiya, Masayuki [1 ,2 ]
Tanaka, Kaori [3 ,4 ]
Linhardt, Robert J. [5 ]
Koketsu, Mamoru [1 ,2 ]
机构
[1] Gifu Univ, Fac Engn, Dept Mat Sci & Technol, 1-1 Yanagido, Gifu 5011193, Japan
[2] Gifu Univ, Fac Engn, Dept Chem & Biomol Sci, 1-1 Yanagido, Gifu 5011193, Japan
[3] Gifu Univ, Life Sci Res Ctr, Div Anaerobe Res, 1-1 Yanagido, Gifu 5011193, Japan
[4] Gifu Univ, United Grad Sch Drug Discovery & Med Informat Sci, 1-1 Yanagido, Gifu 5011193, Japan
[5] Rensselaer Polytech Inst, Ctr Biotechnol & Interdisciplinary Studies, Troy, NY 12180 USA
关键词
Coumarin; Cytoprotection; Human hepatoma HepG2 cell; THERAPEUTIC AGENTS; CONSTITUENTS; PATHWAY; PLANTS; ROOTS;
D O I
10.1016/j.bmcl.2018.06.018
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Coumarins are ubiquitous in higher plants and exhibit various biological actions. The aim of this study was to investigate the structure-activity relationships of coumarin derivatives on tert-butyl hydroperoxide (t-BHP)-induced oxidative damage in human hepatoma HepG2 cells. A series of coumarin derivatives were prepared and assessed for their cytoprotective effects. Among these, a caffeoyl acid-conjugated dihydropyranocoumarin derivative, caffeoyllomatin, efficiently protected against cell damage elicited by t-BHP. Our findings suggest that caffeoyllomatin appears to be a potent cytoprotective agent.
引用
收藏
页码:2422 / 2425
页数:4
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