Triterpene saponins from Antonia ovata leaves

被引:6
|
作者
Magid, Abdulmagid Alabdul [1 ]
Lalun, Nathalie [2 ]
Long, Christophe [3 ]
Borie, Nicolas [1 ]
Bobichon, Helene [4 ]
Moretti, Christian [5 ]
Lavaud, Catherine [1 ]
机构
[1] Inst Chim Mol Reims, IFR 53 Biomol, UMR CNRS 6229, Lab Pharmacognosie, Batiment 18,BP 1039, F-51687 Reims 2, France
[2] UFR Med, IFR Biomol 53, Lab Biol Cellulaire Genet & Histol, F-51095 Reims, France
[3] Ctr Rech & Dev Pierre Fabre, USR CNRS Pierre Fabre ETaC 3388, F-31035 Toulouse 01, France
[4] UFR Med, IFR Biomol 53, UMR CNRS 6237, F-51095 Reims, France
[5] IRD, UMR SAE 138, F-98713 Tahiti, France
关键词
Antonia ovata; Loganiaceae; Triterpenoid saponins; Theasapogenol A; 15 alpha-Hydroxy-theasapogenol A; Cytotoxic activity; ICHTHYOTOXIC PLANTS; FRUITS;
D O I
10.1016/j.phytochem.2012.01.025
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
Six pentacyclic triterpenoid saponins, named antoniosides E-J along with two known alkaloids, were isolated from the leaves of Antonia ovata. Their structures were determined by the extensive use of 1D and 2D-NMR experiments along with HRESIMS analysis and acid hydrolysis. All isolated saponins contained the same pentasaccharide chain: 3-O-[beta-D-glucopyranosyl-(1 -> 2)]-[beta-D-glucopyranosyl-(1 -> 4)]-[beta-D-glucopyranosyl-(1 -> 3)-alpha-L-arabinopyranosyl(1 -> 6)]-beta-D-glucopyranoside, linked at C-3 of esterified derivatives of polyhydroxyoleanene triterpenoids (theasapogenol A and 15 alpha-hydroxy-theasapogenol A). Isolated compounds were evaluated for their cytotoxic activity against KB cell line by a WST-1 assay, and the IC50 values ranged from 3.3 to 5.3 mu M. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:268 / 274
页数:7
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