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20071070088: ½ð±Ò+10 2013-06-19 16:16:22
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20071070088: ½ð±Ò+10 2013-06-19 16:16:22
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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£º¹²²éµ½264¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 21S,23R-21/23,23/27-diepoxy-21-methoxycycloartan-1,24-diene-3,27-dione C31H42O5 ÏàËÆ¶È:61.2% Journal of Natural Products 2009 72 1102-1105 Cycloartane Triterpenoids from KleinhoWia hospita Li-She Gan, Gang Ren, Jian-Xia Mo, Xiang-Yi Zhang, Wei Yao, and Chang-Xin Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . isowalsuranolide C26H30O7 ÏàËÆ¶È:58.6% Journal of Natural Products 2000 63 947-951 Tetranortriterpenoids from Walsura yunnanensis Xiao-Dong Luo, Shao-Hua Wu, Yun-Bao Ma, and Da-Gang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â,6¦Â,7¦Á-trihydroxyolean-12-en-27-oic acid C30H47O4 ÏàËÆ¶È:56.6% Journal of Asian Natural Products Research 2009 11 236-243 Triterpenes from Astilbe chinensis Jun-Yi Hu , Zhi Yao , Ying-Qian Xu , Yoshihisa Takaishi and Hong-Quan Duan Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2¦Á,3¦Á-dihydroxy-30-noroleana-12,20(29)-dien-28-oic acid C29H44O4 ÏàËÆ¶È:55.1% Chemical & Pharmaceutical Bulletin 2003 51(8) 960-965 Triterpenes and Triterpene Saponins from the Stems of Akebia trifoliata Yoshihiro MIMAKI,Minpei KURODA, Akihito YOKOSUKA, Hiroshi HARADA, Masato FUKUSHIMA, and Yutaka SASHIDA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . walsuranolide C26H30O7 ÏàËÆ¶È:55.1% Journal of Natural Products 2000 63 947-951 Tetranortriterpenoids from Walsura yunnanensis Xiao-Dong Luo, Shao-Hua Wu, Yun-Bao Ma, and Da-Gang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . sinomontanine C C34H44N2O9 ÏàËÆ¶È:55.1% Journal of Asian Natural Products Research 2001 3 15-22 Five New Norditerpenoid Alkaloids from Aconitum Sinomontanum FENG-PENG WANG, CHONC-SHENG PENG, XI-XIAN JIAN and DONG-LIN CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . kopsidine A ÏàËÆ¶È:55.1% Natural Product Research 1993 3 291-298 Semisynthesis of Kopsidine a and B via a Polonovski-Potier Reaction Christiane Kan-fan; Jean-Charles Quirion; Henri-Philippe Husson Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 23,24-dihydrocucurbitacin-F ÏàËÆ¶È:55.1% Journal of Natural Products 1987 Vol 50 315 Chemical Studies on Mexican Plants Used in Traditional Medicine, II: Cucurbitacins from Hintonia latiflora Mar¨ªa Teresa Reguero, Rachel Mata, Robert Bye, Edelmira Linares, Guillermo Delgado Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . dihydrocucurbitacin E ÏàËÆ¶È:54.8% Chinese Traditional and Herbal Drugs 2012 43 432-435 Isolation and identification of chemical constituents from Citrullus colocynthis MIAO Jing; ZHANG Jie; DENG Shi-ming; DAI Bin Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 21S,23R-21/23,23/27-diepoxy-21-hydroxycycloartan-1,24-diene-3,27-dione C30H40O5 ÏàËÆ¶È:53.3% Journal of Natural Products 2009 72 1102-1105 Cycloartane Triterpenoids from KleinhoWia hospita Li-She Gan, Gang Ren, Jian-Xia Mo, Xiang-Yi Zhang, Wei Yao, and Chang-Xin Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ulmuestone C38H54O6 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2006 54(6) 775-778 New Triterpenoids Isolated from the Root Bark of Ulmus pumila L. Dong WANG,Mingyu XIA,and Zheng CUI Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . N-ethyl-12-hydroxy-17-veratroyldictizine C31H43NO7 ÏàËÆ¶È:53.3% Phytochemistry 2005 66 837-846 Norditerpene and diterpene alkaloids from Aconitum variegatum Jes¨²s G. D¨ªaz, Juan Garc¨ªa Ruiza, Werner Herz Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 2¦Á,19¦Á-dihydroxy-3-oxo-urs-12-en-28-oic acid ÏàËÆ¶È:53.3% Phytochemistry 2002 59 315-323 Production of bioactive triterpenes by Eriobotrya japonica calli Shoko Taniguchi, Yoko Imayoshi, Eri Kobayashi, Yoshie Takamatsu, Hideyuki Ito,Tsutomu Hatano, Hiroshi Sakagami, Harukuni Tokuda, Hoyoku Nishino,Daigo Sugita, Susumu Shimura, Takashi Yoshida Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2¦Á,19¦Á-dihydroxy-3-oxo-12-ursen-28-oic acid C30H46O5 ÏàËÆ¶È:53.3% Journal of Natural Products 1996 59 643-645 Anti-HIV Triterpene Acids from Geum japonicum Hong-Xi Xu, Fa-Quan Zeng, Min Wan, and Keng-Yeow Sim Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 2¦Á, 19¦Á-di-hydroxyursolic acid C30H48O5 ÏàËÆ¶È:53.3% 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 16 . euscaphic acid C16H24O3 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1989 37 648-651 Cytotoxic Triterpenes from a Chinese Medicine, Goreishi Atsushi NUMATA,Peiming YANG,Chika TAKAHASHI,Ryoko FUJIKI,Michiko NABAE and Eiichi FUJITA Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . cucurbitacin L C30H4407 ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 2000 36 292-294 Bryonia ISOPRENES. II. CUCURBITACIN L AND BRYOAMARIDE FROM Bryonia melanocarpa M. I. lsaev Structure 13C NMR ̼Æ×Ä£Äâͼ |

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