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²éѯ½á¹û£º¹²²éµ½2472¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . CS-E ÏàËÆ¶È:84.8% Chemical & Pharmaceutical Bulletin 1996 44 1834-1848 Isolation of New Tremorgenic Metabolites from an Ascomycete, Corynascus setosus Haruhiro FUJIMOTO,Etsuko NEGISHI,Kentaro YAMAGUCHI,Nahoko NISHI and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Helvolic acid C33H44O8 ÏàËÆ¶È:84.8% Chinese Journal of Applied & Environmental Biology 2007 13 66-68 Chemical Study on Aspergillus sp.136 QIN Ling; LI Bogang; GUAN Jiafa & ZHANG Guolin Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Helvolic acid C33H44O8 ÏàËÆ¶È:80.6% Chinese Journal of Applied & Environmental Biology 2010 16 76-78 Isolation and Anti-phytopathogenic Activity of Secondary Metabolites from Alternaria sp. FL25,an Endophytic Fungus in Ficus carica FENG Chengliang & MA Yangmin Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (4S,5S,6S,8S,9S,10R,13R,14S,16S,17Z)-6,16-diacetoxy-25-hydroxy-3,7-dioxy-29-nordammara-1,17(20)-dien-21-oic acid C33H46O9 ÏàËÆ¶È:75.7% Journal of Natural Products 2008 71(6) 985-989 Cytotoxic Alkaloids and Antibiotic Nordammarane Triterpenoids from the Marine-Derived Fungus Aspergillus sydowi Min Zhang, Wen-Liang Wang, Yu-Chun Fang, Tian-Jiao Zhu, Qian-Qun Gu, and Wei-Ming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . helvolic acid ÏàËÆ¶È:68.9% Chinese Pharmaceutical Journal 2011 46 1154-1158 Metabolites of Aspergillus sp. HT-2 ZHANG, Li-min, LI, Zhan-lina, BAI, Jiao, Wu, Xinc, WANG, Yu, HUA, Hui-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . stigmasta-3,6-dione C29H48O2 ÏàËÆ¶È:65.5% Natural Product Research and Development 2007 19 620-622 Chemical Constituents of Piper pedicellatum C. DC LI Jun-zhu; LIU Hai-yang; DONG Qiu; CHEN Chang-xiang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Helvolic Acid ÏàËÆ¶È:65.5% Lishizhen Medicine and Materia Medica Research 2012 23 1369-1371 Isolation and Identification of the Secondary Metabolites from Endophytic Fungi Ficus carica of FS11 YANG Xiu-fang; XU Xiao-na; ZHANG Hong-chi; MA Yang-min Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ilexhainanin C C30H46O7 ÏàËÆ¶È:63.3% Helvetica Chimica Acta 2007 Vol. 90 121 Triterpenoids from the Leaves of Ilex hainanensis Si-Xiang Zhou, Jun-Shan Yang, Fu-Cheng Liu, and Peng-Fei Tu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . myrioside A C46H78O18 ÏàËÆ¶È:63.3% Chemical & Pharmaceutical Bulletin 2002 50(8) 1097-1099 Five Triterpene Glycosides from Oxytropis myriophylla Masafumi OKAWA,Rie YAMAGUCHI, Hurlad DELGER,Ryota TSUCHIHASHI, Toshihiro NOHARA,Junei KINJO, Susumu ISODA, and Yoshiteru IDA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . rotundic acid C30H48O5 ÏàËÆ¶È:63.3% Phytochemistry 1993 32 417-420 Triterpenoid saponins from Ilex integra Issei Yano, Chikage Nishiizumi, Kazuko Yoshikawa, Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Fupenjic acid C30H44O5 ÏàËÆ¶È:63.3% Korean Journal of Pharmacognosy 2007 38(4) 354-357 Isolation of Two Steroids and a Triterpenoid from the Roots of Potentilla discolor Park, Hee-Juhn; Lee, Kyung-Tae; Park, Jong-Hee Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 6 C31H46O6 ÏàËÆ¶È:63.3% Tetrahedron 2000 56 547-552 Two New 19-Hydroxyursolic Acid-type Triterpenes from Peruvian ¡®Uña de Gato¡¯ (Uncaria tomentosa) Mariko Kitajima, Ken-ichiro Hashimoto, Masashi Yokoya, Hiromitsu Takayama, Norio Aimi Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 2¦Á,19¦Á-dihydroxy-3-oxo-urs-12-en-28-oic acid monoacetate ÏàËÆ¶È:62.5% 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 . rotundic acid ÏàËÆ¶È:62.0% Journal of Natural Products 1999 62 1379-1384 Activity of Triterpenoid Glycosides from the Root Bark of Mussaenda macrophylla against Two Oral Pathogens Nam-Cheol Kim, Anne E. Desjardins, Christine D. Wu, and A. Douglas Kinghorn Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ilexgenin A ÏàËÆ¶È:62.0% Chinese Traditional and Herbal Drugs 2007 38 995-997 붬Çà¸ùÖл¯Ñ§³É·ÖµÄÑо¿ ÒüÎÄÇå;ÖÜÖÐÁ÷;×Þ½ÚÃ÷;ÃϽÜ;¸µ´ºÑà Structure 13C NMR ̼Æ×Ä£Äâͼ |

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