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1 .     urs-12-ene-3¦Â,6¦Â,16¦Â,21¦Â-tetraol-3-O-¦Â-glucopyranoside
C36H60O9     ÏàËÆ¶È:70.2%
Phytochemistry          2008          69          961-972
Triterpene saponins from Silphium radula
Lalita M. Calabria, Sonia Piacente, Ireneusz Kapusta,Suranganie F. Dharmawardhane, Frances M. Segarra, Peter J. Pessiki f, Tom J. Mabry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3-O-¦Â-D-glucopyranosyl 3¦Á,11¦Á-dihydroxylup-20(29)-en-28-oic acid
C36H58O9     ÏàËÆ¶È:67.5%
Phytochemistry          1999          51          1369-1374
Lupane-triterpene glycosides from leaves of Acanthopanax koreanum
Seung-Yeup Chang, Chang-Soo Yook, Toshihiro Nohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     eclalbasaponin VIII
C36H62O8     ÏàËÆ¶È:67.5%
Phytochemistry          1997          44          131-135
Taraxastane glycosides from Eclipta alba
Shoji Yahara, Ning Ding, Toshihiro Nohara, Kazuo Masuda, Hiroyuki Ageta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     2¦Á,3¦Â-dihydroxyurs-12-en-28-oic acid-(28¡ú1)-¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:67.5%
Journal of Natural Products          1994          Vol 57          333
New Triterpenoid Saponins from the Roots of Potentilla tormentilla
A. R. Bilia, E. Palme, S. Catalano, G. Flamini, I. Morelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     methyl 23-benzyloxy-3-oxours-12-en-28-oate
C38H54O4     ÏàËÆ¶È:67.5%
The Journal of Organic Chemistry          2000          65          6278-6282
Synthesis of a-Boswellic Acid Analogues with a Carboxyl Group at C-17 Isolated from the Bark of Schefflera octophylla
Lothar Bore, Tadashi Honda, and Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     lupenic arabinopalmitate
C51H86O6     ÏàËÆ¶È:67.5%
Journal of Asian Natural Products Research          2012          14          7-13
Two new triterpenoids from Cichorium intybus L. roots
Rajkumari Kumari, Mohammed Ali & Vidhu Aeri
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     urs-12-en-28-oic acid-3-O-¦Â-D-glucopyranosyl(1¡ú2)-¦Â-D-glucopyranoside
C42H68O13     ÏàËÆ¶È:66.6%
Indian Journal of Chemistry Section B          1997          36B          901-904
Novel triterpenoid glycosides and triterpenoid acid from the root extract of Acanthus montanus(Acanthace)
Edet M Anam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 17
    ÏàËÆ¶È:65.7%
Chemical & Pharmaceutical Bulletin          2003          51(6)          654-662
Bioactive Constituents from Chinese Natural Medicines. XI.1)Inhibitors on NO Production and Degranulation in RBL-2H3 from Rubia yunnanensis: Structures of Rubianosides II, III, and IV,Rubianol-g, and Rubianthraquinone
Jing TAO, Toshio MORIKAWA, Shin ANDO, Hisashi MATSUDA, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     11,21-dioxo- 3¦Â,15¦Á,24-trihydroxyurs-12-ene-24-O-¦Â-D-glucopyranoside
C36H56O10     ÏàËÆ¶È:64.8%
Journal of Natural Products          2009          72          1563-1567
Triterpenoids and Flavonoids from Celery (Apium graWeolens)
Kailan Zhou, Feng Zhao, Zhihui Liu, Yulei Zhuang, Lixia Chen,and Feng Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     11,21-dioxo-3¦Â,15¦Á,24-trihydroxyolean-12-ene- 24-O-¦Â-D-glucopyranoside
C36H56O10     ÏàËÆ¶È:64.8%
Journal of Natural Products          2009          72          1563-1567
Triterpenoids and Flavonoids from Celery (Apium graWeolens)
Kailan Zhou, Feng Zhao, Zhihui Liu, Yulei Zhuang, Lixia Chen,and Feng Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     rubianoside II
C36H60O8     ÏàËÆ¶È:64.8%
Chemical & Pharmaceutical Bulletin          2003          51(6)          654-662
Bioactive Constituents from Chinese Natural Medicines. XI.1)Inhibitors on NO Production and Degranulation in RBL-2H3 from Rubia yunnanensis: Structures of Rubianosides II, III, and IV,Rubianol-g, and Rubianthraquinone
Jing TAO, Toshio MORIKAWA, Shin ANDO, Hisashi MATSUDA, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     3¦Â,16¦Á-di-O-acetyl-13¦Â, 28-epoxyoleanane
C34H54O5     ÏàËÆ¶È:64.8%
Phytochemistry          2006          67          2641-2650
Oleanane-type triterpenes of Embelia schimperi leaves
Lawrence Onyango Arot Manguro, Steve Onyango Okwiri, Peter Lemmen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     cincholic acid 28-O-¦Â-glucopyranosyl ester
C36H56O10     ÏàËÆ¶È:64.8%
Planta Medica          2005          71          355-361
Six New Triterpenoid Saponins from the Root and Stem Bark of Cephalanthus occidentalis
Zhang, Zhizhen; Li, Shiyou; Zhang, Shanmin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     ilexoside XXV
    ÏàËÆ¶È:64.8%
Chemical & Pharmaceutical Bulletin          1993          41          39-42
Triterpenoid Saponins of Aquifoliaceous Plants. XI.Ilexosides XLI-XLV from the Leaves of Ilex rotunda THUNB.
Kayoko AMIMOTO,Kazuko YOSHIKAWA and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
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