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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£º¹²²éµ½184¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . pukeensine C44H64N2O3 ÏàËÆ¶È:57.5% Acta Pharmaceutica Sinica 1992 27 394-396 A NEW SKELETON BISDITERPENOID ALKALOID FROM ACONITUM PUKEENSE LS Ding; FE Wu; YZ Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . wattoside B C34H57O12 ÏàËÆ¶È:56.4% Acta Botanica Yunnanica 2001 23(3) 373-380 New Steroidal Glycosides from Tupistra wattii YANG Fan, SHEN Ping,WANG Yi-Fei,ZHANG Ren-Yan, YANG Chong-Ren Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Lilioglycoside C C39H60O13 ÏàËÆ¶È:56.4% Chemistry of Natural Compounds 1997 33 658-662 sTRuCTURES OF SOME LILIOGLYCOSIDES FROM THE BULBS OF Lilium regale P. K. Kintya, A. S. Gur'eva, N. E. Mashchenko,and A. S. Shashkov Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Olean-12-en-3¦Â,16¦Â-diol-3-O-palmitate ÏàËÆ¶È:56.4% Pharmazie 2006 61 70-73 Triterpenoids from Pyrethrum tatsienense Yang Ai-Mei, Liu Xia, Lu Run-Hua and Shi Yan-Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . caulophyllogenin-3-O-¦Á-L-arabinopyranoside C35H56O9 ÏàËÆ¶È:56.4% Journal of Anhui Agricultural Sciences 2012 40 745-747 Study on the Chemical Constitutes of C. robustum root MA Yang-min et al Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 10c C38H64O7 ÏàËÆ¶È:56.4% Steroids 2013 78 651-661 Synthesis of various secosteroidal macrocycles by ring-closing metathesis Malika Ibrahim-Ouali, Eug¨¦nie Romero Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-O-¦Â-D-galactopyranosyl-(1¡ú2)-¦Â-D-glucuronopyranosyl quillaic acid ÏàËÆ¶È:54.7% Phytochemistry 1995 40 509-514 Acylated triterpene saponins from Silene jenisseensis Marie-Aleth Lacaille-Dubois, Bernard Hanquet, Zhen-Hua Cui, Zhi-Cen Lou, Hildebert Wagner Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Bupleurosides IV C42H68O14 ÏàËÆ¶È:54.7% Bioorganic & Medicinal Chemistry Letters 1997 7 2193-2198 New hepatoprotective saponins, bupleurosides III, VI, IX, and XIII, from Chinese Bupleuri Radix: Structure-requirements for the cytoprotective activity in primary cultured rat hepatocytes Hisashi Matsuda, Toshiyuki Murakami, Kiyofumi Ninomiya, Masahiro Inadzuki, Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 22-methoxy-(25R)-5¦Â-furostane-1¦Â,3¦Â,4¦Â,5¦Â,26-pentaol 26-O-¦Â-D-glucopyranoside ÏàËÆ¶È:53.8% Acta Botanica Sinica 1999 41 1249-1251 Steroidal saponins from Speirantha gardenii Chen Meng-jing Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . spirasine V/VI ÏàËÆ¶È:53.8% Journal of Integrative Plant Biology 2005 47 120-123 Two New Diterpenoid from Spiraea japonica L.F. var. fortunei (Planchon)Rehd Li-Ming FAN, Hong-Ping HE, Yue-Mao SHENand Xiao-Jiang HAO Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3¦Â,16¦Â,17¦Á-dihydroxycholest-5-en-22-one 16-O-¦Â-D-xylopyranosyl-(1¡ú3)-(2-O-acetyl-¦Á-L-arabinopyranoside C39H62O13 ÏàËÆ¶È:53.8% Phytochemistry 1992 31 3969-3973 Acylated cholestane glycosides from the bulbs of Ornithogalum saundersiae Satoshi Kubo, Yoshihiro Mimaki, Miki Terao, Yutaka Sashida, Tamotsu Nikaido, Taichi Ohmoto Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . olean-12-en-3¦Â,15¦Á-yl diacetate ÏàËÆ¶È:53.8% Phytochemistry 1988 27 3653-3657 Alkaloids from Alstonia macrophylla Atta-ur-rahman,Gulzar Ahmed,M.Iqbal Choudhary,Habib-ur-rehman,K.T. De Silva Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 23-hydroxyimberbic acid-23-O-¦Á-L-4-acetyl-rhamnopyranoside ÏàËÆ¶È:53.8% Chinese Traditional and Herbal Drugs 2008 39 512-514 éÐη糵×ÓÒ¶ÖÐÝÆÀ໯ºÏÎïµÄÑо¿ ÎâÏþÅô;³Â¹âÓ¢;½¯²ÅÎä;Öì¹úÔª;·½ºêÑ« Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ¦Â-amyrin-3-palmitate C46H80O2 ÏàËÆ¶È:53.8% Chinese Journal of Natural Medicines 2007 5 259-262 Non-alkaline Constituents From the Leaf of Alstonia scholaris DU Guo-Shun; CAI Xiang-Hai; SHANG Jian-Hua; LUO Xiao-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . bahamaolide B C39H64O11 ÏàËÆ¶È:53.8% Journal of Natural Products 2012 75 959-967 Bahamaolides A and B, Antifungal Polyene Polyol Macrolides from the Marine Actinomycete Streptomyces sp. Dong-Gyu Kim, Kyuho Moon, Seong-Hwan Kim, Seon-Hui Park, Sunghyouk Park, Sang Kook Lee, Ki-Bong Oh, Jongheon Shin, and Dong-Chan Oh Structure 13C NMR ̼Æ×Ä£Äâͼ |

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