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²éѯ½á¹û£º¹²²éµ½2503¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Arjunaside A C36H56O10 ÏàËÆ¶È:80.5% Planta Medica 2010 76 903-908 18,19-Secooleanane Type Triterpene Glycosyl Esters from the Bark of Terminalia arjuna Wang, Wei; Ali, Zulfiqar; Li, Xing-Cong; Shen, Yunheng; Khan, Ikhlas A. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . kakisaponin C C36H58O10 ÏàËÆ¶È:77.7% Chemical & Pharmaceutical Bulletin 2009 57 532-535 Three Minor Novel Triterpenoids from the Leaves of Diospyros kaki Guang Chen, Zong-Quan Wang and Ji-Ming Jia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Arjunaside E C38H62O11 ÏàËÆ¶È:72.9% Planta Medica 2010 76 903-908 18,19-Secooleanane Type Triterpene Glycosyl Esters from the Bark of Terminalia arjuna Wang, Wei; Ali, Zulfiqar; Li, Xing-Cong; Shen, Yunheng; Khan, Ikhlas A. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Arjunaside B C36H56O11 ÏàËÆ¶È:72.2% Planta Medica 2010 76 903-908 18,19-Secooleanane Type Triterpene Glycosyl Esters from the Bark of Terminalia arjuna Wang, Wei; Ali, Zulfiqar; Li, Xing-Cong; Shen, Yunheng; Khan, Ikhlas A. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Arjunaside C C36H58O10 ÏàËÆ¶È:72.2% Planta Medica 2010 76 903-908 18,19-Secooleanane Type Triterpene Glycosyl Esters from the Bark of Terminalia arjuna Wang, Wei; Ali, Zulfiqar; Li, Xing-Cong; Shen, Yunheng; Khan, Ikhlas A. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 24-epi-pinfaensin ÏàËÆ¶È:69.4% 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 -------------------------------------------------------------------------------- 7 . kakisaponin B C36H58O10 ÏàËÆ¶È:69.4% Chemical & Pharmaceutical Bulletin 2009 57 532-535 Three Minor Novel Triterpenoids from the Leaves of Diospyros kaki Guang Chen, Zong-Quan Wang and Ji-Ming Jia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . swinhoeic acid C30H46O5 ÏàËÆ¶È:67.6% Chinese Traditional and Herbal Drugs 2008 39 978-981 ÈÕ±¾Â·±ßÇàµÄ»¯Ñ§³É·ÖÑо¿ ÕÔ¾§;¸ßÎÄÔ¶;¶ÎºêȪ;ëø½Ü;¸ßʯϲ¾Ã Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . kolokoside A C36H58O10 ÏàËÆ¶È:66.6% Journal of Natural Products 2007 70 378-382 Kolokosides A-D: Triterpenoid Glycosides from a Hawaiian Isolate of Xylaria sp. Stephen T. Deyrup,James B. Gloer, Kerry O¡¯Donnell,and Donald T. Wicklow Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . glucosyl pinfaensate C36H56O11 ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 11 . Laevigin C C36H56O11 ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2013 23 3290-3297 Anti-inflammatory secondary metabolites from the leaves of Rosa laevigata Min, Yan, Yan, Zhu, Hong-Jun, Zhang, Wei-Hua, Jiao, Bing-Nan, Han, Zhao-Xi, Liu, Feng, Qiu, Wan-Sheng, Chen, Hou-Wen, Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . geumonoid C30H46O5 ÏàËÆ¶È:64.7% Chemical & Pharmaceutical Bulletin 2000 48(9) 13647-1369 A New Anti-HIV Triterpene from Geum japonicum Hong-Xi XU,Dong-Sheng MING,Hui Dong,and Paul Pui-Hay BUT Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 18,19-seco,2¦Á,3¦Á-dihydroxyl-19-oxo-urs-11,13(18)-dien-28-oic acid C30H46O5 ÏàËÆ¶È:64.7% Chinese Chemical Letters 2009 20 572-575 Two new triterpenes from Duchesnea indica Wei Qiao, Zhi Yao, Wen Zhang, Hong Quan Duan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 2¦Á,3¦Á-dihydroxy-19-oxo-18,19-seco-urs-11,13(18)-dien-28-oic acid C30H46O5 ÏàËÆ¶È:64.7% Natural Product Research and Development 2005 17 404-408 Triterpene Acids from Toddalia asiatica HUANG Ping*; KARAGIANIS Gloria; WEI Shan-xin; WATERMAN Peter G Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 2¦Á,3R,23-trihydroxy-19-oxo-18,19-seco-urs-11,13(18)-dien-28-oic acid C30H46O6 ÏàËÆ¶È:64.7% Journal of Natural Products 2011 74 732-738 Anti-inflammatory Triterpenes from the Leaves of Rosa laevigata Na Zeng, Yang Shen, Ling-Zhi Li, Wei-Hua Jiao, Pin-Yi Gao, Shao-Jiang Song, Wan-Sheng Chen, and Hou-Wen Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . quadranoside VI C36H56O11 ÏàËÆ¶È:63.8% Chemical & Pharmaceutical Bulletin 2000 48(8) 1114-1120 Quadranosides VI-XI, Six New Triterpene Glucosides from the Seeds of Combretum quadrangulare I Ketut ADNYANA,Yasuhiro TEZUKA, Suresh AWALE,Arjun Hari BANSKOTA, Kim Qui TRAN and Shigetoshi KADOTA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Rosamultin C36H58O10 ÏàËÆ¶È:63.8% 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 -------------------------------------------------------------------------------- 18 . ilexoside XLIII C36H58O11 ÏàËÆ¶È:63.8% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . glucosyl tormentate ÏàËÆ¶È:63.8% 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 -------------------------------------------------------------------------------- 20 . glucosyl tormentate ÏàËÆ¶È:63.8% 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 -------------------------------------------------------------------------------- 21 . 2¦Á,19¦Á-dihydroxy-3-oxo-12-ursen-28-oic acid ¦Â-D-glucopyranosyl ester C36H56O10 ÏàËÆ¶È:63.8% molecules 2011 16 4642-4651 Triterpenoids from the Roots of Sanguisorba tenuifolia var. Alba Hai-Xue Kuang, Hong-Wei Li, Qiu-Hong Wang, Bing-You Yang, Zhi-Bin Wang and Yong-Gang Xia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 28-(O-¦Â-D-Glucopyranosyl)-urs-12-ene-2¦Á,3¦Â,19¦Á-trihydroxy-28-oic acid C36H58O10 ÏàËÆ¶È:63.8% Natural Product Communications 2006 1 705-710 Smooth Muscle Relaxant Triterpenoid Glycosides fromRubus idaeus (Raspberry) Leaves Janne Rojas Vera, Christopher G. Dacke, Gerald Blunden and Asmita V. Patel Structure 13C NMR ̼Æ×Ä£Äâͼ |
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