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1 .     (23E)-lanosta-8,23-diene-3¦Â,25-diol
    ÏàËÆ¶È:83.3%
Phytochemistry          1999          50          849-857
(20R,23E)-Eupha-8,23-diene-3¦Â,25-diol from Tripetalum cymosum
Yuan-Wah Leong, Leslie J. Harrison
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     trematenolic acid
    ÏàËÆ¶È:80%
Chemical & Pharmaceutical Bulletin          2002          50(12)          1603-1606
New Triterpenoids from Tricholoma saponaceum
Kazuko YOSHIKAWA,Mina KUROBOSHI, Shigenobu ARIHARA,Naoko MIURA, Noriyuki TUJIMURA,and Kenji SAKAMOTO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     trametenolic acid
    ÏàËÆ¶È:80%
Journal of Natural Products          2005          68          69-73
Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2
Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     trametenolic acid
    ÏàËÆ¶È:80%
Journal of Natural Products          1999          62          543-545
New Lanostanoid Glycosides from the Fruit Body of Laetiporus versisporus
Kazuko Yoshikawa, Kenji Matsumoto, and Shigenobu Arihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     inotodiol
    ÏàËÆ¶È:80%
Planta Medica          1986          52          495-496
3¦Â,22-Dihydroxylanosta-7,9(11),24-triene: A New, Minor Compound from Inonotus obliquus
Kirsti Kahlos and R. Hiltunen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     inotodiol
    ÏàËÆ¶È:80%
Planta Medica          1984          50          197-198
3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus
Kirsti Kahlos, R. Hiltunen and M. v. Schantz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     euphol
    ÏàËÆ¶È:80%
Acta Pharmaceutica Sinica          1992          27          445-451
TRITERPENE CONSTITUENTS FROM EUPHORBIA NEMTOCYPHA HAND-MAZZ
D Cao; YL Su; JS Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     lanosterol
    ÏàËÆ¶È:80%
Acta Pharmaceutica Sinica          1996          31          524-529
STUDIES ON CHEMICAL CONSTITUENTS OF ROOTS OF EUPHORBIA PEKINENSIS
LY Kong and ZD Min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     euphol (eupha-8,24-di-en-3¦Â-ol)
C30H50O     ÏàËÆ¶È:80%
China Journal of Chinese Materia Medica          2006          31          742-744
Studies on constituents from roots of Euphorbia hylonoma
RUAN Hanli, ZHANG Yue, ZHANG Yonghui, PI Huifang, WU Jizhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     euphol
    ÏàËÆ¶È:80%
China Journal of Chinese Materia Medica          2005          30          1162-1165
Studies on chemical constitutes of green alga Chaetomorpha basiretorsa and their bioactivity
Shi Dayong, HAN Lijun, SUN Jie, YANG Yongchun, SHI Jiangong, FAN Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     euphol
C30H50O     ÏàËÆ¶È:80%
Phytochemistry          1999          50          849-857
(20R,23E)-Eupha-8,23-diene-3¦Â,25-diol from Tripetalum cymosum
Yuan-Wah Leong, Leslie J. Harrison
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




12 .     lanosterol
    ÏàËÆ¶È:80%
Phytochemistry          1999          50          849-857
(20R,23E)-Eupha-8,23-diene-3¦Â,25-diol from Tripetalum cymosum
Yuan-Wah Leong, Leslie J. Harrison
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     trametenolic acid B
    ÏàËÆ¶È:80%
Phytochemistry          1996          41          1041-1046
Antimicrobial steroids from the fungus Fomitopsis pinicola
Anne Caroline Keller, Marc P. Maillard, Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     trametenolic acid
C30H48O3     ÏàËÆ¶È:80%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     euphol
    ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2010          41          877-881
¸ÊË컯ѧ³É·ÖµÄÑо¿
ÎâÏþÀÚ;ÅËÇÚ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     euphol
    ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2008          39          1779-1781
Optimization of purification of Panax notoginseng extract for injection
CHU Yang; SONG Hong-tao; LI Dan; YAN Lu; LIU Dan; CHEN Da-wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     tirucallol
    ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2008          39          1779-1781
Optimization of purification of Panax notoginseng extract for injection
CHU Yang; SONG Hong-tao; LI Dan; YAN Lu; LIU Dan; CHEN Da-wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     lanosterol
C30H50O     ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2005          36          1763-1767
Ingenane diterpene ester constituents from Tibetan medicine Euphorbia wallichii
LI Yu-lin; SUO You-rui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     3¦Â-21-dihydroxy-lanosta-8,24-diene
    ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2001          32          4-6
Studies on chemical constituents of Fuscoporia obliqua
HE Jian; FENG Xiao zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     3¦Â-dihydroxy-lanosta-8,24-diene-21-acid
    ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2001          32          4-6
Studies on chemical constituents of Fuscoporia obliqua
HE Jian; FENG Xiao zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     lanosterol
    ÏàËÆ¶È:80%
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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22 .     lanosterol
    ÏàËÆ¶È:80%
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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23 .     inotodiol
    ÏàËÆ¶È:80%
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

--------------------------------------------------------------------------------




24 .     inotodiol
    ÏàËÆ¶È:80%
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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25 .     24(E)-3¦Â-hydroxylanosta-8,24-dien-26-al-21-oic acid
C30H46O4     ÏàËÆ¶È:80%
The Journal of Antibiotics          2005          59          828-831
A New Cytotoxic Lanostane Triterpenoid from the Basidiomycete Hebeloma versipelle FREE
Hong-Jun Shao, Chen Qing, Fei Wang, Yan-Li Zhang, Du-Qiang Luo and Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     tirucallol
    ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2011          42          251-254
Chemical constituents of Omphalia lapidescens
XU Ming-feng, SHEN Lian-qing, WANG Kui-wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     lanostadienol
    ÏàËÆ¶È:80%
Organic Magnetic Resonance          1974          6          603-611
Carbon-13 NMR spectra of some tetra-and pentacyclic triterpenoids
S. A. Knight
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     euphadienol
    ÏàËÆ¶È:80%
Organic Magnetic Resonance          1974          6          603-611
Carbon-13 NMR spectra of some tetra-and pentacyclic triterpenoids
S. A. Knight
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




29 .     Euphol
C30H50O     ÏàËÆ¶È:80%
Molecules          2012          17          11826-11838
Inhibition of 11b-HSD1 by Tetracyclic Triterpenoids from Euphorbia kansui
Jie Guo, Li-Yan Zhou, Hong-Ping He, Ying Leng, Zhen Yang and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     Euphol
    ÏàËÆ¶È:80%
International Journal of Molecular Sciences          2012          13          11247-11259
Bio-Guided Isolation of the Cytotoxic Terpenoids from the Roots of Euphorbia kansui against Human Normal Cell Lines L-O2 and GES-1
Li Zhang, Lan Gao, Zhengjun Li, Xiaojing Yan, Yanjing Yang, Yuping Tang, Yudan Cao and Anwei Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
¼èÄÑÀ§¿à£¬ÓñÈêÓڳɡ£
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