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²éѯ½á¹û£º¹²²éµ½2415¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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