Cytotoxic abietane-derivative diterpenoids of Salvia lachnostachys

被引:12
|
作者
Oliveira, Cristhian S. [1 ]
Salvador, Marcos J. [2 ]
de Carvalho, Joao E. [3 ]
Santos, Elide P. [4 ]
Barison, Andersson [1 ]
Stefanello, Maria Elida A. [1 ]
机构
[1] Univ Fed Parana, Dept Chem, BR-81531980 Curitiba, Parana, Brazil
[2] Univ Estadual Campinas, Dept Plant Biol, BR-13083970 Campinas, SP, Brazil
[3] Univ Estadual Campinas, CPQBA, BR-13083970 Campinas, SP, Brazil
[4] Univ Fed Parana, Dept Bot, BR-81531990 Curitiba, Parana, Brazil
基金
巴西圣保罗研究基金会;
关键词
Salvia lachnostachys; Lamiaceae; Diterpenes; fruticuline A; Cytotoxic activity; DEMETHYL FRUTICULIN; CORRUGATA;
D O I
10.1016/j.phytol.2016.07.005
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
A bioassay-guided fractionation of Salvia lachnostachys Benth leaf extract led to the isolation of three known diterpenes, namely fruticuline A (1), fruticuline B (2) and 7,20-dihydrofruticuline A (3), together with two new compounds, 4 and 5. The structures were mainly elucidated by 1D and 2D NMR spectroscopy and HRESIMS. The cytotoxic activity of the crude ethanol extract, the semi-purified fractions (A-E) and compounds 1, 2 and 4 were evaluated against seven human cancer cell lines and the normal cell line HaCat. The ethanol extract showed activity against all tested cell lines (GI(50) 25.0-44.0 mu g/mL). Among the fractions, the greatest activity was exhibited by fraction A (eluted with hexane), which inhibited the growth of all tested cell lines with GI(50) of 3.9-19.5 mu g/mL. Compounds 1 and 4 were the most active, inhibiting the growth of U251, MCF-7, NCI-ADR/RES, 786.0, NCI-H460, PC-3, OVCAR-03 and HaCat cell lines with GI(50) < 10 mu M. Compound 2 showed moderate activity against MCF-7, NCI-H460, OVCAR-03, K562 and HaCat, with GI(50) varying 19.9-29.3 mu M. (C) 2016 Phytochemical Society of Europe. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:140 / 143
页数:4
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