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1 .     (5¦Â,6¦Â,15¦Á)-15-Methyllycopodane-5,6-diol
C16H27NO2     ÏàËÆ¶È:68.7%
Helvetica Chimica Acta          2010          93          1187-1191
Two New Lycopodine Alkaloids from Huperzia serrata
Jinhe Jiang, Ying Liu, Kang Min, Bi Jing, Liqin Wang, Yan Zhang and Yegao Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Kandenol D
C15H24O4     ÏàËÆ¶È:66.6%
Journal of Natural Products          2012          75          2223-2227
Kandenols A¨CE, Eudesmenes from an Endophytic Streptomyces sp. of the Mangrove Tree Kandelia candel
Ling Ding, Armin Maier, Heinz-Herbert Fiebig, Wen-Han Lin, Gundela Peschel, and Christian Hertweck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ananosmin acetate
    ÏàËÆ¶È:60%
Acta Botanica Yunnanica          1993          15(2)          196-200
SESQUITERPENOIDS FROM KADSURA ANANOSMA
ZOU Cheng,PU Xiang-Yu,ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Haliclorensin
C13H28N2     ÏàËÆ¶È:60%
Tetrahedron          2001          57          9973-9978
Revision of the structure of haliclorensin to (S)-7-methyl-1,5-diazacyclotetradecane and confirmation of the new structure by synthesis
Markus R Heinrich, Yoel Kashman, Peter Spiteller, Wolfgang Steglich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Saniculamoid C
C15H28O4     ÏàËÆ¶È:60%
Journal of Natural Products          2011          74          1521-1525
Sesquiterpene and Norsesquiterpene Derivatives from Sanicula lamelligera and Their Biological Evaluation
Xue-Song Li, Xiao-Jiang Zhou, Xing-Jie Zhang, Jia Su, Xue-Jing Li, Yong-Ming Yan, Yong-Tang Zheng, Yan Li, Liu-Meng Yang, and Yong-Xian Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (1¦Â,4¦Á,6¦Â)-Gorgonane-1¦Â,4¦Á,11-triol
C15H28O3     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2013          96          445-451
Six Novel Eudesmane-Like Sesquiterpenes from Illicium spathulatum
Xu-Jun Dong and Shi-De Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (4¦Á,7¦Â,9¦Á)-Farfugane-4,9,11-triol
C15H28O3     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2013          96          445-451
Six Novel Eudesmane-Like Sesquiterpenes from Illicium spathulatum
Xu-Jun Dong and Shi-De Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     2-((3S,7S)-3,7-dihydroxy-3-methyldecanamido)ethanesulfonic acid
C13H27NO6S     ÏàËÆ¶È:60%
RSC Advances          2014          4          11073-11079
Taurospongins B and C, new acetylenic fatty acid derivatives possessing a taurine amide residue from a marine sponge of the family Spongiidae†
Takaaki Kubota, Haruna Suzuki, Azusa Takahashi-Nakaguchi, Jane Fromont, Tohru Gonoi and Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     2-((3S,7R)-3,7-dihydroxy-3-methyldecanamido)ethanesulfonic acid
C13H27NO6S     ÏàËÆ¶È:60%
RSC Advances          2014          4          11073-11079
Taurospongins B and C, new acetylenic fatty acid derivatives possessing a taurine amide residue from a marine sponge of the family Spongiidae†
Takaaki Kubota, Haruna Suzuki, Azusa Takahashi-Nakaguchi, Jane Fromont, Tohru Gonoi and Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     equisetumone
C15H24O6     ÏàËÆ¶È:60%
RSC Advances          2014          4          1-3
Equisetumone, a novel 4-5-olide secocaryophyllane sesquiterpene from Equisetum palustre
Zuo-Fu Wei, Yung-Husan Chen, Ping-Jyun Sung, Guey-Horng Wang, Jing-Ru Liou, Sheng-Yang Wang, Shang-Tzen Chang, Yuan Gang Zu, Michael Y. Chiang, Yu-Jie Fu, and Fang-Rong Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     equisetumone
C15H24O6     ÏàËÆ¶È:60%
RSC Advances          2014          4          45749-45752
Equisetumone, a novel 4-5-olide secocaryophyllane sesquiterpene from Equisetum palustre
Zuo-Fu Wei, Yung-Husan Chen, Ping-Jyun Sung, Guey-Horng Wang, Jing-Ru Liou, Sheng-Yang Wang, Shang-Tzen Chang, Yuan Gang Zu, Michael Y. Chiang, Yu-Jie Fu and Fang-Rong Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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