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1 .     glucosyl pinfaensate
C36H56O11     ÏàËÆ¶È:100%
Phytochemistry          1994          36          1469-1472
A triterpene from Rubus pinfaensis
David G. Durham, Xiaojun Liu, R. Michael E. Richards
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     24-epi-pinfaensin
    ÏàËÆ¶È:88.8%
Phytochemistry          1996          42          495-499
Triterpenes and triterpene glycosides from Paradrymonia macrophylla
Christian Terreaux, Marc P. Maillard, Mahabir P. Gupta, Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     2¦Á,3¦Â,19¦Á,23-tetrahydroxyurs-12-ene-28-O-¦Â-D-glucopyranosyl ester (niga-ichigoside F1)
    ÏàËÆ¶È:88.8%
Archives of Pharmacal Research          2011          34          543-550
A dimeric triterpenoid glycoside and flavonoid glycosides with free radical-scavenging activity isolated from Rubus rigidus var. camerunensis
T¨¦lesphore Benoît Nguelefack, F¨¦licit¨¦ Hermine Kamga Mbakam, L¨¦on Az¨¦fack Tapondjou, Pierre Watcho and Elvine Pami Nguelefack-Mbuyo, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     niga-ichigoside F1
    ÏàËÆ¶È:86.1%
Chemical & Pharmaceutical Bulletin          2003          51(2)          200-202
A New Triterpene Glucosyl Ester from the Fruit of the Blackberry (Rubus allegheniensis)
Masateru ONO,Michiko TATEISHI, Chikako MASUOKA,Hiromasa KOBAYASHI,Keiji IGOSHI,Haruki KOMATSU,Yasuyuki ITO,Masafumi OKAWA,and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     tormentoside
    ÏàËÆ¶È:86.1%
Planta Medica          1995          61          94-95
Tormentoside and Two of its Isomers Obtained from the Rhizomes of Potentilla erecta
Lech Stachurski, Elbi eta Bednarek Jan Cz. Dobrowolski, Halina Strzelecka, and Aleksander P. Mazurek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Rosamultin
C36H58O10     ÏàËÆ¶È:86.1%
Acta Botanica Yunnanica          2008          30(1)          121-124
Triterpenoids from Saurauia napaulensis (Saurauiaceae)
WANGQiong,JU Peng,WANG Yi-Fen,LUO Shi-De
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     niga-ichigoside F1
C36H58O11     ÏàËÆ¶È:86.1%
Acta Botanica Yunnanica          2008          30(1)          121-124
Triterpenoids from Saurauia napaulensis (Saurauiaceae)
WANGQiong,JU Peng,WANG Yi-Fen,LUO Shi-De
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     suavissimoside R1
C36H54O12     ÏàËÆ¶È:86.1%
Chemical & Pharmaceutical Bulletin          1985          33          37-40
19¦Á-Hydroxyursane-Type Triterpene Glucosyl Esters from the Roots of Rubus suavissimus S. LEE
FENG GAO,FENGHUAI CHEN,TAKASHI TANAKA,RYOJI KASAI,TAKASHI SETO and OSAMU TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     suavissimoside R1
C36H56O12     ÏàËÆ¶È:86.1%
Chemical & Pharmaceutical Bulletin          1987          35          1748-1754
Trachelosperosides, Glycosides of 19¦Á-Hydroxyursane-Type Triterpenoids from Trachelospermum asiaticum (Trachelospermum. III)
FUMIKO ABE and TATSUO YAMAUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     trachelosperoside A-1
C36H56O12     ÏàËÆ¶È:86.1%
Chemical & Pharmaceutical Bulletin          1987          35          1748-1754
Trachelosperosides, Glycosides of 19¦Á-Hydroxyursane-Type Triterpenoids from Trachelospermum asiaticum (Trachelospermum. III)
FUMIKO ABE and TATSUO YAMAUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     trachelosperoside B-1
C36H58O12     ÏàËÆ¶È:86.1%
Chemical & Pharmaceutical Bulletin          1987          35          1748-1754
Trachelosperosides, Glycosides of 19¦Á-Hydroxyursane-Type Triterpenoids from Trachelospermum asiaticum (Trachelospermum. III)
FUMIKO ABE and TATSUO YAMAUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     suavissmoside R1
    ÏàËÆ¶È:86.1%
Natural Product Research          2002          16          137-141
Aculeoside I, A Novel 18,19-Seco-ursane Saponin Isolated from Ilex Aculeolata
Ming-An Ouyang; Xu Zhang; Dian-Peng Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     niga-ichigoside F1
C36H58O11     ÏàËÆ¶È:86.1%
China Journal of Chinese Materia Medica          1994          19          486-487
Studies on the Chemical Constituents of Chinese Medicianl Plant Rubus parviforlius L.
Wang Xianrong, Du Anquan and Wang Hongping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     sauvissimoside R1
C36H56O12     ÏàËÆ¶È:86.1%
China Journal of Chinese Materia Medica          1994          19          486-487
Studies on the Chemical Constituents of Chinese Medicianl Plant Rubus parviforlius L.
Wang Xianrong, Du Anquan and Wang Hongping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Niga-ichigoside F1
    ÏàËÆ¶È:86.1%
Fitoterapia          2001          72          591-593
Saponins from Strasburgeria robusta
B.H. Um, T. Pouplin, A. Lobstein, B. Weniger,M. Litaudon, R. Anton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 2
    ÏàËÆ¶È:86.1%
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   Ì¼Æ×Ä£Äâͼ
17 .     glucosyl tormentate
    ÏàËÆ¶È:86.1%
Acta Pharmaceutica Sinica          2008          Vol 43          504-508
Triterpene saponins from Adinandra nitida
WANG Ying; YE Wen-cai; YIN Zhi-qi; ZHAO Shou-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     niga-ichigoside F1
    ÏàËÆ¶È:86.1%
Acta Pharmaceutica Sinica          2001          Vol 36          910-912
TRITERPENOIDS FROM CLEMATOCLETHRA SCANDENS
ZHANG Xiao rong; PENG Shu lin; WANG Ming kui; DING Li sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     19¦Á-hydroxyasiatic acid
    ÏàËÆ¶È:86.1%
Phytochemistry          1994          36          1469-1472
A triterpene from Rubus pinfaensis
David G. Durham, Xiaojun Liu, R. Michael E. Richards
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Rosmutin
    ÏàËÆ¶È:86.1%
Phytochemistry          1993          32          155-159
Triterpenoids from Sanguisorba alpina
Zhong-Jian Jia, Xiang-Qian Liu, Zi-Min Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     4-epi-niga-ichigoside F1
C36H58O11     ÏàËÆ¶È:86.1%
Phytochemistry          1992          31          3642-3644
Oleanane and ursane glucosides from Rubus species
Zhou Xiao-Hong, Ryoji Kasai, Kazuhiro Ohtani, Osamu Tanaka, Nie Rui-Lin, Yang Chong-Ren, Zhou Jun, Kazuo Yamasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     glucosyl tormentate
    ÏàËÆ¶È:86.1%
Phytochemistry          1992          31          3642-3644
Oleanane and ursane glucosides from Rubus species
Zhou Xiao-Hong, Ryoji Kasai, Kazuhiro Ohtani, Osamu Tanaka, Nie Rui-Lin, Yang Chong-Ren, Zhou Jun, Kazuo Yamasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     tormentic acid ester glucoside
C36H58O10     ÏàËÆ¶È:86.1%
Phytochemistry          1988          27          3593-3595
Saponins from leaves of Aphloia theiformis
Naidu Gopalsamy,David Vargas,Joseph Gu¨¦ho,Claude Ricaud,Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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