Isolation, modification and cytotoxic evaluation of stilbenoids from Acanthopanax leucorrhizus

被引:8
作者
Hu, Hao-Bin [1 ]
Liang, Hai-Peng [2 ]
Li, Hai-Ming [1 ]
Yuan, Ru-Nan [3 ]
Sun, Jiao [3 ]
Zhang, La-La [1 ]
Han, Ming-Hu [1 ]
Wu, Yun [1 ]
机构
[1] Longdong Univ, Coll Chem & Chem Engn, Qingyang 745000, Peoples R China
[2] Qingyang First Peoples Hosp, Dept Oncol, Qingyang 745000, Peoples R China
[3] Gansu Agr Univ, Coll Food Sci & Engn, Lanzhou 730070, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
Cytotoxicity; Stilbenoids; Acanthopanax leucorrhizus; Structure-activity relationship; ROOT BARK; CONSTITUENTS; RESVERATROL; ANTIOXIDANT;
D O I
10.1016/j.fitote.2017.11.007
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Twenty natural stilbenoids (1 - 20), including seven new stilbenoids (2, 4-7, 19, 20) and thirteen known stilbenoids (1, 3, 8-18), were isolated from the stem barks of Acanthopanax ieucorrhizus, and six modified stilbenoid derivatives (1a, 2a, 4a, 4b, 7a and 17a) were obtained via methylation, demethylation and isopentenylation of the corresponding isolates (1, 2, 4, 7 and 17). These stilbenoids were structurally characterized by comprehensive analysis of their spectroscopic data and comparison with literature information, and evaluated for their cytotoxic activities against three human tumor cell lines (leukemia HL-60, hepatoma SMMC-7721 and breast carcinoma MCF-7) in vitro by MIT assay. The results showed that compounds 1a, 4a and 4b showed potent selective cytotoxicity against SMMC-7721 (IC50 = 10.16 +/- 1.95 mu M and 9.76 +/- 1.32 mu M) and MCF-7 (IC50 = 10.72 mu 2.78 mu M) cell lines. The cytotoxic evaluation of these structurally modified stilbenoid derivatives have led to the establishment of a structure-activity relationship.
引用
收藏
页码:167 / 176
页数:10
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