一种新的细胞毒性糖脑苷。

M. D. Kaoke, Denis Kehdinga Sema, J. Dzoyem, P. B. Leutcha, F. Delie, E. Allémann, Wilfred Fon, N. Sewald, A. Lannang
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引用次数: 3

摘要

本文研究了喀麦隆药用植物巨叶罗菲亚(Rauvolfia macrophylla Stapf)茎皮次生代谢产物对人白血病细胞系THP-1(小鼠单核细胞白血病细胞系)和小鼠巨噬细胞系Raw264.7(人巨噬细胞白血病细胞系)的抗增殖活性。一种新的脑糖苷,Rauvocerebroside(1)与其他六种已知化合物;分离得到11-甲氧基-19-epiajmalicine(2)、19-epiajmalicine(3)、蔗糖(4)、丁丁酸(6)和Lupeol(7)。利用一维和二维核磁共振、红外和质谱数据以及已发表的综述对它们的结构进行了阐明。对化合物(1)、(2)和(3)的细胞毒性分析表明,化合物(1)对THP-1 (IC50为20.70 μM)和Raw 264.7 (IC50为26.34 μM)癌细胞具有较好的活性。化合物(2)和(3)对THP-1细胞的IC50为43.23 μM(2)和34.25 μM(3),对Raw 264.7细胞的IC50较低。这些结果表明化合物(1)、(2)和(3)可能是潜在的抗癌剂。
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A New Cytotoxic Glycocerebroside from Rauvolfia macrophylla Stapf.
The present study investigated secondary metabolites from stem bark of a Cameroonian medicinal plant Rauvolfia macrophylla Stapf, and their anti-proliferative activities against human leukaemia cell lines, THP-1 (mouse monocytic leukaemia cell lines) and mouse macrophage cell line Raw264.7 (human macrophage leukaemia cell lines). One new glycocereboside, Rauvocerebroside (1) with six other known compounds,; 11-methoxy-19-epiajmalicine (2), 19-epiajmalicine (3), Sucrose (4), Butulinic acid (6) and Lupeol (7) were isolated. Their structural elucidation was done using 1D and 2D NMR, IR and MS spectroscopy data together with published reviews. Analyses of the cytotoxicity of compounds (1), (2) and (3) displayed good activity of (1) on THP-1 (IC50 20.70 μM) and Raw 264.7 (IC50 26.34 μM) cancer cell lines. Compounds (2) and (3), showed moderate activity on THP-1 cells (IC50 43.23 μM for (2) and 34.25 μM for (3) and a low activity on Raw 264.7 cells. These results suggest that compounds (1), (2) and (3) could be potential anticancer agent.
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