Preparation and cytotoxic effect of ceanothic acid derivatives

被引:23
作者
Lee, SS [1 ]
Chen, WC
Huang, CF
Su, Y
机构
[1] Natl Taiwan Univ, Coll Med, Sch Pharm, Taipei 10018, Taiwan
[2] Natl Yang Ming Univ, Inst Pharmacol, Taipei 112, Taiwan
来源
JOURNAL OF NATURAL PRODUCTS | 1998年 / 61卷 / 11期
关键词
D O I
10.1021/np9800856
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Six ceanothane and 1-norceanothane derivatives (1, 2, 8-11) were prepared from ceanothic acid dibenzyl ester. These ring-A homologues of betulinic acid exhibited cytotoxic effects. Among these, 1-decarboxy-3-oxo-ceanothic acid (2) was found to be the most cytotoxic against OVCAR-3 and HeLa cancer cell lines, with an IC50 of 2.8 and 6.6 mu g/mL, respectively, and an IC50 of 11.3 mu g/mL against normal cell line FS-5.
引用
收藏
页码:1343 / 1347
页数:5
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