Triterpene saponins of Genista ulicina Spach

被引:19
作者
Boutaghane, Naima [1 ,2 ]
Voutquenne-Nazabadioko, Laurence [1 ]
Harakat, Dominique [1 ]
Simon, Alain
Kabouche, Zahia [2 ]
机构
[1] UFR Pharm, CNRS UMR 7312, ICMR, F-51687 Reims, France
[2] Univ Mentouri Constantine, Fac Sci Exactes, Lab Obtent Subst Therapeutiques, Constantine 25000, Algeria
关键词
Genista ulicina; Fabaceae; Triterpenoid saponins; Cytotoxic activity; QUINOLIZIDINE ALKALOIDS; SOYASAPONIN-I; FLAVONOIDS; PLANTS; ISOFLAVONOIDS; SESSILIFOLIA; ELUCIDATION; SAPOGENOL; TENERA;
D O I
10.1016/j.phytochem.2013.03.020
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
From the n-BuOH extract of the aerial parts of Genista ulicina, six triterpene saponins, 3-O-beta-D-glucopyranosyl-olean-12-ene-3 beta,27,28,30-tetraol, 3-O-beta-D-glucopyranosyl-olean-12-ene-3 beta,27,28,29-tetraol, 3,29-di-O-beta-D-glucopyranosyl-olean-12-ene-3 beta,27,28,29-tetraol, 3-O-beta-D-glucopyranosyl-olean-12-ene-3 beta,28,29-triol-27-oic acid, 3-O-beta-D-glucopyranosyl-olean-12-ene-3 beta,27,28-triol-29-oic acid, and 3-O-beta-D-glucopyranosyl-14-H-27-nor-olean-12-ene-3 beta,28,29-triol, were isolated together with eight known triterpene saponins and six flavonoids. Their structures were established mainly by means of spectroscopic methods (1D and 2D-NMR as well as HR-ESI-MS). The n-BuOH extract, investigated for its antitumor growth inhibition of human colon cancer HT-29 cells, presented no significant activity (IC50 > 100 mu g). (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:176 / 181
页数:6
相关论文
共 37 条
[1]   UNAMBIGUOUS H-1-NMR AND C-13-NMR ASSIGNMENTS OF ISOFLAVONES FROM VIROLA-CADUCIFOLIA [J].
DOSSANTOS, SA ;
DE CARVALHO, MG ;
BRAZ FILHO, R .
JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY, 1995, 6 (04) :349-352
[2]   Identification of medicinal plants in the family Fabaceae using a potential DNA barcode ITS2 [J].
Gao, Ting ;
Yao, Hui ;
Song, Jingyuan ;
Liu, Chang ;
Zhu, Yingjie ;
Ma, Xinye ;
Pang, Xiaohui ;
Xu, Hongxi ;
Chen, Shilin .
JOURNAL OF ETHNOPHARMACOLOGY, 2010, 130 (01) :116-121
[3]   Assessment of estrogenic activity of flavonoids from Mediterranean plants using an in vitro short-term test [J].
Garritano, S ;
Pinto, B ;
Giachi, I ;
Pistelli, L ;
Reali, D .
PHYTOMEDICINE, 2005, 12 (1-2) :143-147
[4]   Flavonoids and isoflavonoids from Genista morisii [J].
Giachi, I ;
Manunta, A ;
Morelli, I ;
Pistelli, L .
BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 2002, 30 (08) :801-803
[5]  
Harborne J. B., 1994, PHYTOCHEMICAL DICT L, P313
[6]  
Ilarionov I, 1979, FARMATSIYA, V29, P39
[7]   Major triterpenoid saponins from Saponaria officinalis [J].
Jia, ZH ;
Koike, K ;
Nikaido, T .
JOURNAL OF NATURAL PRODUCTS, 1998, 61 (11) :1368-1373
[8]   SAPONIN AND SAPOGENOL .45. STRUCTURES OF KAIKASAPONIN-I, KAIKASAPONIN-II, AND KAIKASAPONIN-III FROM SOPHORAE FLOS, THE BUDS OF SOPHORA-JAPONICA L [J].
KITAGAWA, I ;
TANIYAMA, T ;
HONG, WW ;
HORI, K ;
YOSHIKAWA, M .
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 1988, 108 (06) :538-546
[9]  
KITAGAWA I, 1976, CHEM PHARM BULL, V24, P121
[10]   CONSTITUENTS OF LEGUMINOUS PLANTS .13. NEW TRITERPENOID SAPONINS FROM WISTARIA-BRACHYBOTRYS [J].
KONOSHIMA, T ;
KOZUKA, M ;
HARUNA, M ;
ITO, K .
JOURNAL OF NATURAL PRODUCTS, 1991, 54 (03) :830-836