Bioactive Constituents from Michelia champaca

被引：0
|
作者：
Yeh, Yu-Ting [2 ]
Huang, Jin-Cherng [3 ]
Kuo, Po-Lin [1 ]
Chen, Chung-Yi [2 ]
机构：
[1] Kaohsiung Med Univ, Inst Clin Med, Kaohsiung 807, Taiwan
[2] Fooyin Univ, Sch Med & Hlth Sci, Kaohsiung 831, Taiwan
[3] Natl Chiayi Univ, Dept Forest Prod Sci & Furniture Engn, Chiayi 600, Taiwan
来源：
NATURAL PRODUCT COMMUNICATIONS | 2011年 / 6卷 / 09期
关键词：
Michelia champaca L; aporphine; liriodenine; CYTOTOXIC CONSTITUENTS; THERAPY; APOPTOSIS; ALKALOIDS; RECEPTOR; LEAVES; CELLS;
D O I：
暂无
中图分类号：
R914 [药物化学];
学科分类号：
100701 ;
摘要：
(-)-Anonaine (1), (-)-asimilobine (2), (-)-nuciferine (3), (-)-anolobine (4), (-)-romerine (5), (-)-N-acetylanonaine (6), liriodenine (7), (+)-syringaresinol (8), N-trans-feruloyltyramine (9), N-cis-feruloyltyramine (10), scopoletin (11), 4-acetonyl-3,5-dimethoxy-p-quinol (12), vanillin (13), vanillic acid (14), syringic acid (15), beta-sitosterol (16) and stigmasterol (17) were isolated from branches of Michelia champaca L. In addition, a cell proliferation assay of five of the isolated compounds on human breast and lung cancer cells showed that liriodenine (7) was the strongest inhibitor.
引用
收藏
页码：1251 / 1252
页数：2
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