Steroidal saponins from the leaves of Beaucarnea recurvata

被引：11

作者：

Eskander, Jacqueline ^{[1
,3
]}

Lavaud, Catherine ^{[1
]}

Harakat, Dominique ^{[2
]}

机构：

[1] UMR CNRS 6229, ICMR, Lab Pharmacognosie, F-51687 Reims 2, France

[2] UMR CNRS 6229, ICMR, Serv Anal, F-51687 Reims 2, France

[3] Helwan Univ, Fac Pharm, Dept Pharmacognosy, Cairo, Egypt

来源：

PHYTOCHEMISTRY | 2011年 / 72卷 / 09期

关键词：

Beaucarnea recurvata; Ruscaceae; Steroidal saponins; INHIBITORY-ACTIVITY; STRUCTURAL ELUCIDATION; GLYCOSIDES; SEEDS; STEMS;

D O I：

10.1016/j.phytochem.2011.03.004

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：

Thirteen steroidal saponins were isolated from the leaves of Beaucarnea recurvata Lem. Their structures were established using one- and two-dimensional NMR spectroscopy and mass spectrometry. Six of them were identified as: 26-O-beta-D-glucopyranosyl (25S)-furosta-5,20(22)-diene 1 beta,3 beta,26-triol 1-O-alpha-L-rhamnopyranosyl-(1 -> 2) beta-D-fucopyranoside, 26-O-beta-D-glucopyranosyl (25S)-furosta-5,20(22)-diene 1 beta,3 beta,26-triol 1-O-alpha-L-rhamnopyranosyl-(1 -> 2)-4-O-acetyl-beta-D-fucopyranoside, 26-O-beta-D-glucopyranosyl (25R)-furosta-5,20(22)-diene-23-one-1 beta,3 beta,26-triol 1-O-alpha-L-rhamnopyranosyl-(1 -> 2) beta-D-fucopyranoside, 26-O-beta-D-glucopyranosyl (25S)-furosta-5-ene-1 beta,3 beta,22 alpha,26-tetrol 1-O-alpha-L-rhamnopyranosyl-(1 -> 4)-6-O-acetyl-beta-D-glucopyranoside, 26-O-beta-D-glucopyranosyl (25S)-furosta-5-ene-1 beta,3 beta,22 alpha,26-tetrol 1-O-alpha-L-rhamnopyranosyl-(1 -> 2) beta-D-fucopyranoside, and 24-O-beta-D-glucopyranosyl (25R)-spirost-5-ene-1 beta,3 beta, 24-triol 1-O-alpha-L-rhamnopyranosyl-(1 -> 2)-4-O-acetyl-beta-D-fucopyranoside. The chemotaxonomic classification of B. recurvata in the family Ruscaceae was discussed. (C) 2011 Elsevier Ltd. All rights reserved.

引用

页码：946 / 951

页数：6

共 30 条

[1] Dependence of 1H NMR chemical shifts of geminal protons of glycosyloxy methylene (H2-26) on the orientation of the 27-methyl group of furostane-type steroidal saponins [J].

Agrawal, PK .

MAGNETIC RESONANCE IN CHEMISTRY, 2004, 42 (11) :990-993

[2] NMR-SPECTROSCOPY IN THE STRUCTURAL ELUCIDATION OF OLIGOSACCHARIDES AND GLYCOSIDES [J].

AGRAWAL, PK .

PHYTOCHEMISTRY, 1992, 31 (10) :3307-3330

[3]

[Anonymous], 1997, Cactus and succulent plants: Status survey and conservation action plan

[4]

[Anonymous], 2003, BOT J LINN SOC, V141, P399, DOI DOI 10.1046/J.1095-8339.2003.T01-1-00158.X

[5] Saponins from Allium minutiflorum with antifungal activity [J].

Barile, Elisa ;

Bonanomi, Giuliano ;

Antignani, Vincenzo ;

Zolfaghari, Behzad ;

Sajjadi, S. Ebrahim ;

Scala, Felice ;

Lanzotti, Virginia .

PHYTOCHEMISTRY, 2007, 68 (05) :596-603

[6] Spirostanol saponins of Allium porrum L. [J].

Carotenuto, A ;

Fattorusso, E ;

Lanzotti, V ;

Magno, S .

PHYTOCHEMISTRY, 1999, 51 (08) :1077-1082

[7] A subfamilial classification for the expanded asparagalean families Amaryllidaceae, Asparagaceae and Xanthorrhoeaceae [J].

Chase, Mark W. ;

Reveal, James L. ;

Fay, Michael F. .

BOTANICAL JOURNAL OF THE LINNEAN SOCIETY, 2009, 161 (02) :132-136

[8]

COMBARIEU ED, 2002, FITOTERAPIA, V73, P583

[9] Saponins and flavonoids of Allium triquetrum [J].

Corea, G ;

Fattorusso, E ;

Lanzotti, V .

JOURNAL OF NATURAL PRODUCTS, 2003, 66 (11) :1405-1411

[10]

DING Y, 1989, PHYTOCHEMISTRY, V28, P2787, DOI 10.1016/S0031-9422(00)98089-0

← 1 2 3 →