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

页码：1251 / 1252

页数：2

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