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1 .     Mogroside I E1
C36H62O9     ÏàËÆ¶È:82.3%
Chinese Journal of Natural Medicines          2010          8          21-24
Chemical Constituents from the Stems and Leaves of Elaeocarpus glabripetalus
ZHANG Sheng; TAO Zheng-Ming; ZHANG Yi; SHEN Zheng-Wu; QIN Guo-Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2 .     24-¦Á-ethyl-20-ene-7-hydro-stigmast-8¦Â:14¦Â-di-3-O-¦Â-D-xylofuranoside
C34H58O6     ÏàËÆ¶È:58.8%
Asian Journal of Chemistry          1995          7          490-494
A New Steroidal Saponin from Trichosanthes dioica (Roxb.)
V.K. Saxena and R.K. Dave
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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3 .     3¦Â-O-5,25-stigmastadien¦Â-D-glucopyranoside
C35H58O6     ÏàËÆ¶È:58.8%
West China Journal of Pharmaceutical Sciences          2011          26          420-423
The separation and indentification of biflavonoids from Androsace umbellata
WANG Wen-jing, LEI Jun, XIAO Yun-chuan, XI Zhen, YU Min, HUANG Jing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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4 .     Snatzkein A
    ÏàËÆ¶È:58.3%
Magnetic Resonance in Chemistry          1997          35          637-642
Structures of Two Novel Triterpene Saponins from Arenaira filicaulis Boiss.
M. Hani A. Elgamal, Hesham S. M. Soliman, Dalal T. Elmunajjed, G¨¢bor T¨®th, Andr¨¢s Simon and Helmut Duddeck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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5 .     3¦Á,27-dihydroxy-cycloart-24E-en-26-oic acid
C30H48O     ÏàËÆ¶È:57.5%
Phytochemistry          1989          28          1471-1477
Triterpenoids from Mangifera indica
V. Anjaneyulu,K. Ravi,K.Harischandra Prasad,J.D. Connolly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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6 .     neomacrotriol
C31H52O3     ÏàËÆ¶È:57.5%
Phytochemistry          2014          102          189-196
Cycloartane triterpenes from the leaves of Neoboutonia macrocalyx L. Original Research Article
Jane Namukobe, Bernard T. Kiremire, Robert Byamukama, John M. Kasenene, Vincent Dumontet, Françoise Gu¨¦ritte, Sabrina Krief, Isabelle Florent, John D. Kabasa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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7 .     uvariol
    ÏàËÆ¶È:57.5%
Lishizhen Medicine and Materia Medica Research          2006          17          1178-1181
Chemical Constituents of Inonotus obliquus
ZHAO Fen-qin, PIAO Hui-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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8 .     cholesteryl-3-O-¦Â-D-glucoside
    ÏàËÆ¶È:57.5%
Strait Pharmaceutical Journal          2012          24          50-53
Studies on Chemical Constituents of Livistona chinesis
CHEN Yan, YAO Hong, LI Shao-guang, HUANG Li-ying, LIN Xin-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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9 .     Cimicifugadine
C35H51NO8     ÏàËÆ¶È:57.1%
Organic Letters          2007          Vol. 9, No. 9          1813-1816
Cimicifugadine from Cimicifuga foetida,a New Class of Triterpene Alklaoids with Novel Reactivity
Chun Dan, Yan Zhou, Deng Ye,Shulin Peng, Lisheng Ding,Michael L. Gross, and Samuel X. Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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10 .     24-hydroxyolean-12-en-3¦Â-yl-¦Â-D-glucopyranoside
C36H60O7     ÏàËÆ¶È:55.5%
Chemical & Pharmaceutical Bulletin          2010          58          1093-1095
Two New Aristolochic Acid Derivatives from the Roots of Aristolochia fangchi and Their Cytotoxicities
Yu Cai and Tian-Ge Cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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11 .     Cycloccidentaliside I
    ÏàËÆ¶È:55.5%
Planta Medica          2012          78          821-827
Li, Shi-Fei; Di, Ying-Tong; Luo, Rong-Hua; Zheng, Yong-Tang; Wang, Yue-Hu; Fang, Xin; Zhang, Yu; Li, Ling; He, Hong-Ping; Li, Shun-Lin; Hao, Xiao-Jiang:
Cycloartane Triterpenoids from Cassia occidentalis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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12 .     9¦Â,25-cyclo 3¦Â-O-(¦Â-D-glucopyranosyl)echynocystic acid
C36H56O9     ÏàËÆ¶È:55.5%
Journal of Ethnopharmacology          2011          135          78-87
Chemical constituents from the stem bark of Symplocos paniculata Thunb. with antimicrobial, analgesic and anti-inflammatory activities
Ruchi Badoni Semwal, Deepak Kumar Semwal, Ravindra Semwal, Randhir Singh, Mohan Singh Maniyari Rawat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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13 .     2,22-dideoxy-20-hydroxyecdysone 25-O-¦Â-D-glucopyranoside
C33H54O10     ÏàËÆ¶È:54.5%
Phytochemistry          2009          70          430-436
Ecdysteroids and a sucrose phenylpropanoid ester from Froelichia floridana
Ping Wang, Shiyou Li, Stacy Ownby, Zhizhen Zhang, Wei Yuan, Wanli Zhang, R. Scott Beasley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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14 .     glyyunnansapogenin B2
    ÏàËÆ¶È:54.5%
Acta Pharmaceutica Sinica          1995          30          27-33
NEW TRTEKPENOIDAL SAPOGENINS FROM THE ROOTS OF GLYCYRRHIZA YUNNANENSIS
JF Hu; ZL Ye and FJ Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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15 .     butyrospermol acetate
    ÏàËÆ¶È:54.5%
China Journal of Chinese Materia Medica          2003          28          124-126
Studies on Chemical Constituents from the Bark of Morus macroura
WU Feng, SUN Shengguo, CHEN Ruoyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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16 .     lup-20(30)-ene-3¦Á,29-diol
C30H50O2     ÏàËÆ¶È:54.5%
Phytochemistry          1999          50          839-841
A pentacyclic triterpene from Daphne oleoides
Nisar Ullah, Zaheer Ahmed, Saeed Ahmed, Pir Muhammad, Abdul Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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17 .     ocotillol
    ÏàËÆ¶È:54.5%
Journal of Shenyang Pharmaceutical University          2008          25          35-38
Chemical constitunts from Sonneratia ovata
ZHENG Zhe, PEI Yue-hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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18 .     penasterol
C30H48O3     ÏàËÆ¶È:54.5%
Journal of the Chemical Society, Perkin Transactions 1          1988                   2403-2406
Penasterol, a novel antileukemic sterol from the okinawan marine sponge Penares sp.
Jie-fei Cheng, Jun'ichi Kobayashi, Hideshi Nakamura, Yasushi Ohizumi, Yoshimasa Hirata and Takuma Sasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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19 .     trametenolicacid
    ÏàËÆ¶È:54.5%
Natural Product Research and Development          2010          22          433-436
Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus
ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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20 .     (20R,22R)-2¦Â,3¦Â:20,22-bis(isopropylidenedioxy)-5¦Â-cholest-8(14)-ene-6¦Â,25-diol
    ÏàËÆ¶È:54.5%
Russian Journal of Organic Chemistry          2008          44          671-674
Analogs of ecdysteroids with a tetrasubstituted ¦¤8,14-bond
V. N. Odinokov, R. V. Shafikov, R. G. Savchenko, S. R. Afon¡¯kina and I. V. Galyautdinov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Óë¾ý³õÏàʶ£¬ÓÌÈç¹ÊÈ˹顣
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