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CD3OD£º11.59,15.18,16.52,18.06,21.00,23.41,25.17,25.69,25.84,26.91,27.69,28.34,32.79,36.92,37.54,40.62,41.21,41.51,42.97,47.86,48.08,53.45,61.16,69.81,70.46,72.28.72.50,76.93,77.17,79.30,79.97,94.39,129.54,137.06,177.18
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hylgxib: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-23 07:24:12
1 .     kaji-ichigoside F1
    ÏàËÆ¶È:80.5%
Journal of China Pharmaceutical University          2002          33          184-187
Studies on the Constituents of Rosa multiflora Thunb
LI Yan Fang*; HU Li Hong; LOU Feng Chang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     1¦Â,2¦Á,3¦Á-trihydroxyurs-12-en-28-oic acid (1¦Â-hydroxyeuscaphic acid)
C30H48O6     ÏàËÆ¶È:77.1%
Natural Product Sciences          2009          15          76-82
NMR Assignment and Antimicrobial/Antioxidant Activities of 1¦Â-Hydroxyeuscaphic acid from the Seeds of Butyrospermum parkii
Nyaa, Laurentine Bouquet Tankeu; Tapondjou, Leon Azefack; Barboni, Luciano; Tamokou, Jean De Dieu; Kuiate, Jules Roger; Tane, Pierre; Park, Hee-Juhn
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     emarginellic acid
C30H18O5     ÏàËÆ¶È:75%
Phytochemistry          2006          67          956-964
Crotalic and emarginellic acids: Two triterpenes from Crotalaria emarginella and anti-inflammatory and anti-hepatotoxic activity of crotalic acid
Bahar Ahmed , Tawfeq A. Al-Howiriny, Jaber S. Mossa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     kaji-ichigoside F1
C36H60O10     ÏàËÆ¶È:75%
Chinese Journal of Natural Medicines          2010          8          12-15
Triterpenoids from the Roots of Rose odorata var.gigantean
LIU Dai-Lin; ZHU Shan; MA Rong; ZHANG Jing-Ze; LI He-Yu; CHEN Hong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     potentillanoside A
C36H56O10     ÏàËÆ¶È:75%
Phytochemistry          2014          102          169-181
Hepatoprotective triterpenes from traditional Tibetan medicine Potentilla anserina
Toshio Morikawa, Kiyofumi Ninomiya, Katsuya Imura, Takahiro Yamaguchi, Yoshinori Akagi, Masayuki Yoshikawa, Takao Hayakawa, Osamu Muraoka
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     ilexsaponin B
C36H56O11     ÏàËÆ¶È:75%
Asian Journal of Chemistry          2013          25          9457-9459
Qtriterpenoides from the Leaves of Ilex pubescens and their Potential Xanthine Oxidase Inhibitory Activity
ZHONG-LIU ZHOU, *, ZONG-CAI FENG and JING-MIN XIA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     methyl-1¦Á,2¦Á,3¦Â,19¦Á-tetrahydroxyurs-12-en-28-oate
C31H50O6     ÏàËÆ¶È:74.2%
Phytochemistry          1998          49          2477-2481
Pentacyclic triterpenoids from Rubus xanthocarpus
Bao-Zhi Li, Bin-Gui Wang, Zhong-Jian Jia
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     derivative of methyl tormentate
C35H54O7     ÏàËÆ¶È:74.2%
Phytochemistry          1998          48          171-174
Cecropioic acid, a pentacyclic triterpene from Musanga cecropioides
D. Lontsi, B. L. Sondengam, M. T. Martin, B. Bodo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     niga-ichigosideF1
    ÏàËÆ¶È:74.2%
Natural Product Research and Development          2014          26          215-217
Chemical Constituents from the Water-soluble Fraction of Rabdosia excisa
TANG Jian, MA Rui-li, LIU Hong-chuan, OUYANG Zhen, CHEN Hai-sheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     rubuside J
C36H56O11     ÏàËÆ¶È:72.2%
Journal of Natural Products          2009          72          1755-1760
Triterpenoid Saponins from Rubus ellipticus var. obcordatus
Wei Li, Hongwei Fu, Hong Bai, Tatsunori Sasaki, Hiroyoshi Kato, and Kazuo Koike
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     ilexoside XXX
C36H56O11     ÏàËÆ¶È:72.2%
Chemical & Pharmaceutical Bulletin          1992          40          3138-3141
Triterpenoid Saponins of Aquifoliaceous Plants. VIII. Ilexosides XXIX-XXXII from the Leaves of Ilex rotunda THUNB.
Kayoko AMIMOTO,Kazuko YOSHIKAWA and Shigenobu ARIHARA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     compound 2
    ÏàËÆ¶È:72.2%
Phytochemistry          1996          42          505-508
Unsaturated E-ring triterpenes from rubus pinfaensis
David G. Durham, Iain X. Liu, R. Michael E. Richards
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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