Phytochemical and bioactivity studies on constituents of the leaves of Vitex quinata

被引:22
作者
Deng, Ye [1 ]
Chin, Young-Won [1 ]
Chai, Hee-Byung [1 ]
de Blanco, Esperanza Carcache [1 ,2 ]
Kardono, Leonardus B. S. [3 ]
Riswan, Soedarsano [4 ]
Soejarto, Djaja D. [5 ]
Farnsworth, Norman R. [5 ]
Kinghorn, A. Douglas [1 ]
机构
[1] Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USA
[2] Ohio State Univ, Coll Pharm, Div Pharm Practice & Adm, Columbus, OH 43210 USA
[3] Indonesian Inst Sci, Serpong 15310, Tangerang, Indonesia
[4] Indonesian Inst Sci, Biol Res Ctr, Herbarium Bogoriense, Bogor 16122, Indonesia
[5] Univ Illinois, Coll Pharm, Chicago, IL 60612 USA
基金
美国国家卫生研究院;
关键词
Cytotoxicity; (S)-5-Hydroxy-7,4 '-dimethoxyflavanone; Methyl 3,4,5-O-tricaffeoyl quinate; Methyl 10R-methoxy-12-oxo-9(13); 16E-Phytodienoate; NF-kappa B assay; 3,4,3 ',4 '-Tetrahydroxy-delta-truxinate; Vitex quinata; FLAVONOIDS;
D O I
10.1016/j.phytol.2011.03.007
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
A phytochemical investigation of the leaves of Vitex quinata (Lour.) F.N. Williams (Verbenaceae), guided by a cytotoxicity assay against the MCF-7 human breast cancer cell line, led to the isolation of a new delta-truxinate derivative (1) and a new phytonoic acid derivative (2), together with 12 known compounds. The structures of the new compounds were determined by spectroscopic methods as dimethyl 3,4,3 ',4 '-tetrahydroxy-delta-truxinate (1) and methyl 10R-methoxy-12-oxo-9(13), 16E-phytodienoate (2), respectively. In a cytotoxicity assay, (S)-5-hydroxy-7,4 '-dimethoxyflavanone (3) was found to be the sole active principle, with ED50 values of 1.1-6.7 mu M, respectively, when tested against a panel of three human cancer cells. Methyl 3,4,5-O-tricaffeoyl quinate (4) showed activity in an enzyme-based ELISA NF-kappa B p65 assay, with an ED50 value of 10.3 mu M. (C) 2011 Phytochemical Society of Europe. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:213 / 217
页数:5
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