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纤细卷柏中的细胞毒性双黄酮类化合物。

Cytotoxic biflavonoids from Selaginella delicatula.

作者信息

Lin L C, Kuo Y C, Chou C J

机构信息

National Research Institute of Chinese Medicine, Pettou, Taipei 112, Taiwan, Republic of China.

出版信息

J Nat Prod. 2000 May;63(5):627-30. doi: 10.1021/np990538m.

Abstract

Four new biflavonoids-robustaflavone 4'-methyl ether (1), robustaflavone 7,4'-dimethyl ether (2), 2",3" -dihydrorobustaflavone 7,4', -dimethyl ether (3), and 2",3" '-dihydrorobustaflavone 7,4', 7"-trimethyl ether (4)-as well as two known biflavonoids, robustaflavone and amentoflavone, and three caffeoylquinic acids, 3,5-di-O-caffeoylquinic acid, 3, 4-di-O-caffeoylquinic acid, and 4,5-di-O-caffeoylquinic acid, were isolated from Selaginella delicatula. The structures of the new compounds were established by spectroscopic analysis and chemical modification. The cytotoxic activity of these compounds on various tumor cell lines was evaluated, and both compounds 1 and 3 significantly suppressed the growth of Raji and Calu-1 tumor cell lines.

摘要

从薄叶卷柏中分离出4种新的双黄酮类化合物——粗壮黄酮4'-甲醚(1)、粗壮黄酮7,4'-二甲醚(2)、2",3"-二氢粗壮黄酮7,4'-二甲醚(3)和2",3"'-二氢粗壮黄酮7,4',7"-三甲醚(4),以及2种已知的双黄酮类化合物——粗壮黄酮和穗花杉双黄酮,还有3种咖啡酰奎宁酸——3,5-二-O-咖啡酰奎宁酸、3,4-二-O-咖啡酰奎宁酸和4,5-二-O-咖啡酰奎宁酸。通过光谱分析和化学修饰确定了新化合物的结构。评估了这些化合物对各种肿瘤细胞系的细胞毒性活性,化合物1和3均显著抑制了Raji和Calu-1肿瘤细胞系的生长。

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