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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
15 .     ilexgenin A
    ÏàËÆ¶È:62.0%
Chinese Traditional and Herbal Drugs          2007          38          995-997
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Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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