Triterpene saponins from Cyclamen hederifolium

被引:39
作者
Altunkeyik, Hilal [2 ]
Gulcemal, Derya [2 ]
Masullo, Milena [1 ]
Alankus-Caliskan, Ozgen [2 ]
Piacente, Sonia [1 ]
Karayildirim, Tamer [2 ]
机构
[1] Univ Salerno, Dipartimento Sci Farmaceut & Biomed, I-84084 Fisciano, Italy
[2] Ege Univ, Fac Sci, Dept Chem, TR-35100 Izmir, Turkey
关键词
Cyclamen hederifolium; Oleanane-type saponins; ARDISIA-CRENATA; ANTIINFLAMMATORY ACTIVITY; BIOLOGICAL-ACTIVITIES; TRADITIONAL MEDICINE; COUM; PERSICUM;
D O I
10.1016/j.phytochem.2011.09.003
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
Five triterpene saponins never reported before, hederifoliosides A-E, and four known triterpene saponins were isolated from the tubers of Cyclamen hederifolium. The structures of hederifoliosides A-E were determined as 3 beta,16 alpha-dihydroxy-13 beta,28-epoxyolean-30-oic acid 3-O-{[beta-D-glucopyranosyl-(1 -> 2)-O]-beta-D-xylopyranosyl-(1 -> 2)-O-beta-D-glucopyranosyl-(1 -> 4)-O-alpha-L-arabinopyranoside}, 3 beta,16 alpha-dihydroxy-13 beta, 28-epoxyolean-30-oic acid 3-O-{[beta-D-glucopyranosyl-(1 -> 2)-O]-beta-D-xylopyranosyl-(1 -> 2)-O-[beta-D-glucopyranosyl-(1 -> 3)]-O-beta-D-glucopyranosyl-(1 -> 4)-O-alpha-L-arabinopyranoside}, 3 beta,16 alpha-dihydroxy-13 beta, 28-epoxyolean-30-al 3-O-{[beta-D-glucopyranosyl-(1 -> 2)-O]-beta-D-xylopyranosyl-(1 -> 2)-O-[beta-D-glucopyranosyl-(1 -> 3)]-O-[beta-D-glucopyranosyl-(1 -> 6)]-O-beta-D-glucopyranosyl-(1 -> 4)-O-alpha-L-arabinopyranoside}, 30-O-beta-D-glucopyranosyl-(1 -> 2)-O -beta-D-glucopyranosyl-3 beta,16 alpha,30-trihydroxyolean-12-en-28-al 3-O-{[beta-D-glucopyranosyl-(1 -> 2)-O]-beta-D-xylopyranosyl-(1 -> 2)-O-beta-D-glucopyranosyl-(1 -> 4)-O-alpha-L-arabinopyranoside}, 30-O-beta-D-glucopyranosyl-(1 -> 2)-O-beta-D-glucopyranosyl-3 beta,16 alpha,28,30-tetrahydroxyolean-12-en 3-O-{[beta-D-glucopyranosyl-(1 -> 2)-O]-beta-D-xylopyranosyl-(1 -> 2)-O-[beta-D-glucopyranosyl-(1 -> 3)]-O-beta-D-glucopyranosyl-(1 -> 4)-O-alpha-L-arabinopyranoside}, by a combination of one- and two-dimensional NMR techniques, and mass spectrometry. The cytotoxic activity of the isolated compounds was evaluated against a small panel of cancer cell lines including Hela, H-446, HT-29, and U937. None of the tested compounds, in a range of concentrations between 1 and 50 mu M, caused a significant reduction of the cell number. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:127 / 133
页数:7
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