Dihydroxyxanthones prenylated derivatives: Synthesis, structure elucidation, and growth inhibitory activity on human tumor cell lines with improvement of selectivity for MCF-7

被引:53
作者
Castanheiro, Raquel A. P.
Pinto, Madalena M. M. [1 ]
Silva, Artur M. S.
Cravo, Sara M. M.
Gales, Luis
Damas, Ana M.
Nazareth, Nair
Nascimento, Maria S. J.
Eaton, Graham
机构
[1] Univ Porto, Ctr Estudos Quim Organ Fitoquim & Farmacol, Oporto, Portugal
[2] Univ Porto, Fac Farm, Lab Quim Organ, P-4050047 Oporto, Portugal
[3] Univ Aveiro, Dept Quim, P-3810193 Aveiro, Portugal
[4] Univ Porto, Inst Ciencias Biomed Abel Salazar, ICBAS, P-4099003 Oporto, Portugal
[5] Univ Porto, IBMC, Unidad Estructura Mol, P-4050047 Oporto, Portugal
[6] Univ Porto, Fac Farm, Microbiol Lab, P-4050047 Oporto, Portugal
[7] Univ Leicester, Dept Chem, Leicester LE 7RH, Leics, England
关键词
xanthones; Prenylation; antitumor activity; x-ray crystallography; NMR spectroscopy;
D O I
10.1016/j.bmc.2007.06.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The synthesis, structure elucidation, and antitumor activity of 11 xanthones are reported, being the compounds 3, 4, 6-8, and 9 described for the first time. Xanthones 1 and 2 were used as building blocks to obtain the prenylated derivatives 3-8. Prenylation was carried out using prenyl bromide in alkaline medium. Dihydropyranoxanthones 9-11 were obtained from compounds 4 and 5 by an oxidative ring closure. The structure of the compounds was established by IR, UV, MS, and NMR (H-1, C-13, Cosy, HSQC, and HMBC techniques and for compounds 4, 6, and 11 the structure was confirmed by X-ray crystallographic analysis. The effect of the 11 xanthones on the in vitro growth of four human tumor cell lines, MCF-7 (breast adenocarcinoma), NCI-H460 (nonsmall cell lung cancer), SF-268 (central nervous system cancer), and UACC-62 (melanoma) is also described. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6080 / 6088
页数:9
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