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²éѯ½á¹û£º¹²²éµ½11¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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