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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.
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页码:140 / 143
页数:4
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