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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½4410¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

2Â¥2013-12-10 16:15:24
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3Â¥2013-12-10 16:46:19














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