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1 .     21¦Â-Hydroxyserrat-14-en-3-one
     ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          1992          28          575-579
POLYFUNCTIONAL TRITERPENOIDS FROM THE BARK OF YEDDO SPRUCE
G. F. Chernenko, I. Yu. Bagryanskaya,Yu. V. Gatilov, G. E. Sal'nikov,E. N. Shmidt, and V. I. Mamatyuk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


2 .     serrat-14-en-3¦Â,21¦Â,24,29-tetraol
C30H50O4     ÏàËÆ¶È:66.6%
Natural Product Research          2004          18          453-459
Serratane-type Triterpenoids from Huperzia Serrata
Hui Zhou; Yun-Sen Li; Xiao-Tian Tong; Hui-Qing Liu; Shan-Hao Jiang; Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


3 .     euscaphic acid
     ÏàËÆ¶È:66.6%
China Journal of Chinese Materia Medica          2007          32          496-500
Studies on chemical constituents in fruits of Eucalyptus globulus
YANG Xiuwei, GUO Qingmei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


4 .     3,21-diepiserratenediol
C30H50O2     ÏàËÆ¶È:66.6%
Phytochemistry          1994          37          209-211
Serratenes from the stem bark of Picea Jezoensis carr. hondoensis
Reiko Tanaka, Rie Tsuboi, Shunyo Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


5 .     24-(E)-3-oxo-dammara-6-¦Â-hydroxy-20,24-dien-26-al
C30H46O3     ÏàËÆ¶È:66.6%
Tetrahedron          1997          53          6465-6472
First examples of dammarane triterpenes isolated from Celastraceae
Haydee Ch¨¢vez, Ana Est¨¦vez-Braun, Ángel G. Ravelo, Antonio G. Gonz¨¢lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


6 .     3¦Â-Butynyloxy-5,6-epoxycholestane
     ÏàËÆ¶È:64.5%
Steroids          2007          72          729-735
6E-Hydroximinosteroid homodimerization by cross-metathesis processes
Miriam Rega, Carlos Jim¨¦nez, Jaime Rodr¨ªguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


7 .     27-hydroxyambrein
C30H54O3     ÏàËÆ¶È:63.3%
Journal of Natural Products          2007          70          147-153
Chemical Transformation and Biological Activities of Ambrein, a Major Product of Ambergris from Physeter macrocephalus (Sperm Whale)
Ya-Ching Shen,Shi-Yie Cheng,Yao-Haur Kuo,Tsong-Long Hwang,Michael Y. Chiang,and Ashraf Taha Khalil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


8 .     yunganogenin C
     ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          1995          43          636-640
Five New Triterpene Glycosides from Wisteria branchybotrys (Leguminosae)
Junei KINJO,Yoshie FUJISHIMA,Kazuyo SAINO,Rui-hua TIAN and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


9 .     compound 11b
     ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          1988          36          1646-1663
Tannins and Related Compounds. LXVII. : Isolation and Characterization of Castanopsinins A-H, Novel Ellagitannins Containing a Triterpenoid Glycoside Core, from Castanopsis cuspidata var. sieboldii NAKAI. (3)
MASAYUKI AGETA,GEN-ICHIRO NONAKA and ITSUO NISHIOKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


10 .     Soyasapogenol B
C30H50O3     ÏàËÆ¶È:63.3%
Journal of Asian Natural Products Research          2005          7          237-243
Three new isoprenylated flavonoids from the roots of Sophora flavescens
PEI-LAN DING, AI-JUN HOU and DAO-FENG CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


11 .     (22S,23S,24R)-24-methyl-22,23-epoxy-3¦Á,5-cyclo-5¦Á-cholestan-6¦Â-yl acetate
     ÏàËÆ¶È:63.3%
Journal of Natural Products          1985          Vol 48          756-765
Starfish Saponins, Part 22. Asterosaponins from the Starfish Halityle regularis: A Novel 22,23-Epoxysteroidal Gylcoside Sulfate
Raffaele Riccio, Maria Iorizzi, Olinda Squillace Greco, Luigi Minale, Maurice Debray, Jean Luis Menou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


12 .     daucosterol
     ÏàËÆ¶È:63.3%
Natural Product Sciences          2009          15          181-184
Phytochemical Constituents from the Seeds of Lithospermum erythrorhizon
Park, Jun-Yeon; Lee, Sul-Lim; Han, Saem; Kim, Hye-Min; Lee, Jeong-Min; Ahn, Young-Hee; Lee, Sook-Young; Lee, Sang-Hyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


13 .     21¦Â-Hydroxyserrat-14-en-3-one
C30H48O2     ÏàËÆ¶È:63.3%
Phytochemistry          1994          37          209-211
Serratenes from the stem bark of Picea Jezoensis carr. hondoensis
Reiko Tanaka, Rie Tsuboi, Shunyo Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


14 .     olibanumol H
C30H52O3     ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          2009          57          957-964
Absolute Stereostructures of Olibanumols A, B, C, H, I, and J from Olibanum, Gum-Resin of Boswellia carterii, and Inhibitors of Nitric Oxide Production in Lipopolysaccharide-Activated Mouse Peritoneal Macrophages
Masayuki Yoshikawa, Toshio Morikawa, Hideo Oominami and Hisashi Matsuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


15 .     uvaol
     ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2002          33          888-889
ËÄ´¨Áúµ¨µÄÈýÝÆ³É·Ö
Nam joon-young,ÁõÏòǰ,ÕųÐìÇ,³Êç¼§,Àî¼Ãîç,½²ýä¨
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


16 .     compound 3
C31H50     ÏàËÆ¶È:63.3%
Tetrahedron Letters          2004          45          3093-3096
Enzymatic cyclization of 26- and 27-methylidenesqualene to novel unnatural C31 polyprenoids by squalene:hopene cyclase
Hideya Tanaka, Hiroshi Noguchi, Ikuro Abe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


17 .     12-ursine-3,28-diol
     ÏàËÆ¶È:63.3%
Natural Product Research and Development          2008          20          821-823
Studies on the Chemical Constituents of Ilex cornuta
ZHANG Jie; YU Rong; WU Xia; YE Yun-hua; ZHOU Ya-wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


18 .     ursolic acid
     ÏàËÆ¶È:63.3%
Natural Product Research and Development          2006          18          942-944
Chemical Constituents of Hedyotis diffusa
SI Jian-yong; CHEN Di-hua*; PAN Rui-le; ZHAO Xiao-hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


19 .     betulinic acid
     ÏàËÆ¶È:63.3%
Records of Natural Products          2013          7          65-68
Chemical Constituents, Antimicrobial and Cytotoxic Activities of Hypericum riparium (Guttiferae)
Michel F. Tala1, Patricia D. Tchakam, Hippolyte K. Wabo, Ferdinand M. Talontsi, Pierre Tane, Jules R. Kuiate, L¨¦on A. apondjou and Hartmut Laatsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


20 .     dysoxyhainic acid D
C30H46O4     ÏàËÆ¶È:63.3%
European Journal of Organic Chemistry          2009          2009          4818-4824
Ring A Modified Novel Triterpenoids from Dysoxylum hainanense
Xiu-Feng He, Xiao-Ning Wang, Sheng Yin, Lei Dong and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


21 .     (25S)-5¦Á-Spirostan-25-ol
C27H44O3     ÏàËÆ¶È:63.3%
Organic Magnetic Resonance          1977          9          439-464
13C N.m.r. Spectra of steroids¡ªA Survey and Commentary
J.W.Blunt and J.B.Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


22 .     Lupeportlandol
C30H50O     ÏàËÆ¶È:63.3%
Journal of the Brazilian Chemical Society          2004          15          742-747
Isoprenoid Compounds from Euphorbia portlandica. X-ray Structure of Lupeportlandol, a New Lupane Triterpene
Ana M. Madureira, Maria Teresa Duarte, Maria F¨¢tima M. Piedade Jos¨¦ R. Ascenso and Maria-Jos¨¦ U. Ferreira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1 .     21¦Â-Hydroxyserrat-14-en-3-one
    ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          1992          28          575-579
POLYFUNCTIONAL TRITERPENOIDS FROM THE BARK OF YEDDO SPRUCE
G. F. Chernenko, I. Yu. Bagryanskaya,Yu. V. Gatilov, G. E. Sal'nikov,E. N. Shmidt, and V. I. Mamatyuk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     serrat-14-en-3¦Â,21¦Â,24,29-tetraol
C30H50O4     ÏàËÆ¶È:66.6%
Natural Product Research          2004          18          453-459
Serratane-type Triterpenoids from Huperzia Serrata
Hui Zhou; Yun-Sen Li; Xiao-Tian Tong; Hui-Qing Liu; Shan-Hao Jiang; Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     euscaphic acid
    ÏàËÆ¶È:66.6%
China Journal of Chinese Materia Medica          2007          32          496-500
Studies on chemical constituents in fruits of Eucalyptus globulus
YANG Xiuwei, GUO Qingmei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3,21-diepiserratenediol
C30H50O2     ÏàËÆ¶È:66.6%
Phytochemistry          1994          37          209-211
Serratenes from the stem bark of Picea Jezoensis carr. hondoensis
Reiko Tanaka, Rie Tsuboi, Shunyo Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     24-(E)-3-oxo-dammara-6-¦Â-hydroxy-20,24-dien-26-al
C30H46O3     ÏàËÆ¶È:66.6%
Tetrahedron          1997          53          6465-6472
First examples of dammarane triterpenes isolated from Celastraceae
Haydee Ch¨¢vez, Ana Est¨¦vez-Braun, ¨¢ngel G. Ravelo, Antonio G. Gonz¨¢lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3¦Â-Butynyloxy-5,6-epoxycholestane
    ÏàËÆ¶È:64.5%
Steroids          2007          72          729-735
6E-Hydroximinosteroid homodimerization by cross-metathesis processes
Miriam Rega, Carlos Jim¨¦nez, Jaime Rodr¨ªguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     27-hydroxyambrein
C30H54O3     ÏàËÆ¶È:63.3%
Journal of Natural Products          2007          70          147-153
Chemical Transformation and Biological Activities of Ambrein, a Major Product of Ambergris from Physeter macrocephalus (Sperm Whale)
Ya-Ching Shen,Shi-Yie Cheng,Yao-Haur Kuo,Tsong-Long Hwang,Michael Y. Chiang,and Ashraf Taha Khalil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     yunganogenin C
    ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          1995          43          636-640
Five New Triterpene Glycosides from Wisteria branchybotrys (Leguminosae)
Junei KINJO,Yoshie FUJISHIMA,Kazuyo SAINO,Rui-hua TIAN and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 11b
    ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          1988          36          1646-1663
Tannins and Related Compounds. LXVII. : Isolation and Characterization of Castanopsinins A-H, Novel Ellagitannins Containing a Triterpenoid Glycoside Core, from Castanopsis cuspidata var. sieboldii NAKAI. (3)
MASAYUKI AGETA,GEN-ICHIRO NONAKA and ITSUO NISHIOKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Soyasapogenol B
C30H50O3     ÏàËÆ¶È:63.3%
Journal of Asian Natural Products Research          2005          7          237-243
Three new isoprenylated flavonoids from the roots of Sophora flavescens
PEI-LAN DING, AI-JUN HOU and DAO-FENG CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (22S,23S,24R)-24-methyl-22,23-epoxy-3¦Á,5-cyclo-5¦Á-cholestan-6¦Â-yl acetate
    ÏàËÆ¶È:63.3%
Journal of Natural Products          1985          Vol 48          756-765
Starfish Saponins, Part 22. Asterosaponins from the Starfish Halityle regularis: A Novel 22,23-Epoxysteroidal Gylcoside Sulfate
Raffaele Riccio, Maria Iorizzi, Olinda Squillace Greco, Luigi Minale, Maurice Debray, Jean Luis Menou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     daucosterol
    ÏàËÆ¶È:63.3%
Natural Product Sciences          2009          15          181-184
Phytochemical Constituents from the Seeds of Lithospermum erythrorhizon
Park, Jun-Yeon; Lee, Sul-Lim; Han, Saem; Kim, Hye-Min; Lee, Jeong-Min; Ahn, Young-Hee; Lee, Sook-Young; Lee, Sang-Hyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     21¦Â-Hydroxyserrat-14-en-3-one
C30H48O2     ÏàËÆ¶È:63.3%
Phytochemistry          1994          37          209-211
Serratenes from the stem bark of Picea Jezoensis carr. hondoensis
Reiko Tanaka, Rie Tsuboi, Shunyo Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     olibanumol H
C30H52O3     ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          2009          57          957-964
Absolute Stereostructures of Olibanumols A, B, C, H, I, and J from Olibanum, Gum-Resin of Boswellia carterii, and Inhibitors of Nitric Oxide Production in Lipopolysaccharide-Activated Mouse Peritoneal Macrophages
Masayuki Yoshikawa, Toshio Morikawa, Hideo Oominami and Hisashi Matsuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     uvaol
    ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2002          33          888-889
ËÄ´¨Áúµ¨µÄÈýÝÆ³É·Ö
Nam joon-young,ÁõÏòǰ,ÕųÐìÇ,³Êç¼§,Àî¼Ãîç,½²ýä¨
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 3
C31H50     ÏàËÆ¶È:63.3%
Tetrahedron Letters          2004          45          3093-3096
Enzymatic cyclization of 26- and 27-methylidenesqualene to novel unnatural C31 polyprenoids by squalene:hopene cyclase
Hideya Tanaka, Hiroshi Noguchi, Ikuro Abe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     12-ursine-3,28-diol
    ÏàËÆ¶È:63.3%
Natural Product Research and Development          2008          20          821-823
Studies on the Chemical Constituents of Ilex cornuta
ZHANG Jie; YU Rong; WU Xia; YE Yun-hua; ZHOU Ya-wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     ursolic acid
    ÏàËÆ¶È:63.3%
Natural Product Research and Development          2006          18          942-944
Chemical Constituents of Hedyotis diffusa
SI Jian-yong; CHEN Di-hua*; PAN Rui-le; ZHAO Xiao-hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
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