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²éѯ½á¹û£º¹²²éµ½16¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . lingshuiolide B C15H22O4 ÏàËÆ¶È:53.3% Journal of Natural Products 2008 71(8) 1399-1403 Sesquiterpenes from the Hainan Sponge Dysidea septosa Xiao-Chun Huang, Jia Li, Zhen-Yu Li, Lei Shi, and Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . tricho-acorenol C15H26O ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1995 43 1035-1038 Studies on Metabolites of Mycoparasitic Fungi. III. New Sesquiterpene Alcohol from Trichoderma koningii Qing HUANG,Yasuhiro TEZUKA,Yasumaru HATANAKA,Tohru KIKUCHI,Arasuke NISHI and Keisuke TUBAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â-hydroxycostic acid ÏàËÆ¶È:53.3% Natural Product Research 1997 11 1-4 Eudesmane Derivatives from Flourensia thurifera: Structure and Biological Activity Francesca Faini; Cecilia Labbe; Rene Torres; Giuliano Delle Monache; Franco Delle Monache; Jose Coll Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (-)-Nootkatene ÏàËÆ¶È:53.3% Phytochemistry 1993 33 1147-1155 Fragrant sesquiterpenes from agarwood Masakazu Ishihara, Tomoyuki Tsuneya, Kenji Uneyama Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (-)-guaia-1(10),11-dien-15-carboxylic acid C15H22O1 ÏàËÆ¶È:53.3% Phytochemistry 1991 30 3343-3347 Guaiane sesquiterpenes from agarwood Masakazu Ishihara, Tomoyuki Tsuneya, Kenji Uneyama Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (6S)-2-methyl-6-[(1R,5S)-(4-methene-5-hydroxyl-2-cyclohexen)-2-hepten-4-one] ÏàËÆ¶È:53.3% Chinese Journal of Medicinal Chemistry 2007 17 238-241 Chemical constituents of Curcuma longa: bisabolane sesquiterpenes ZENG Yong-chi, LIANG Jian-mou, QU Ge-xia, QIU Feng Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-O-[¦Á-rhamnopyranosyl-(1-4)-¦Â-O-glucopyranosyl-(1-4)-¦Â-O-glucopyranosyl]-rishitin ÏàËÆ¶È:53.3% Agricultural and Biological Chemistry 1985 49 2537-2541 Three New Sesquiterpenoid Glycosides from Tobacco Hisashi KODAMA, Takane FUJIMORI, Kunio KATO Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . plakorsin D C15H24O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2013 76 600-606 Cytotoxic Polyketide Derivatives from the South China Sea Sponge Plakortis simplex Jinrong Zhang, Xuli Tang, Jing Li, Peifeng Li, Nicole J. de Voogd, Xiaoqin Ni, Xiaojie Jin, Xiaojun Yao, Pinglin Li, and Guoqiang Li Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 12-hydroxynootkatone C15H22O2 ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 2013 49 457-461 Eremophilane-type sesquiterpenes from Alpinia oxyphylla with inhibitory activity against nitric oxide production Junju Xu, Jia Su, Yan Li, Ninghua Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 4-Hydroxy-1,3(15),10-bisabolatrien-9-one ÏàËÆ¶È:53.3% Natural Product Communications 2008 3 1649-1652 Guaiane Sesquiterpenoids from Jatropha curcas Xia-Chang Wang, Shi-Ping Ma,, Jing-Han Liu and Li-Hong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2-Methyl-4-pentenol C13H24O2 ÏàËÆ¶È:53.3% Journal of Chemical Ecology 1992 18 637-657 Introduction of methyl groups to acetate substituted chain of (Z)-5-decenyl acetate, a pheromone component of turnip moth,agrotis segetum: synthesis, single-sensillum recordings, and structure-activity relationships Stig Jönsson, Tommy Liljefors, Bill S. Hansson Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (-)-bicyclogermacra-1(10)(E),4(E)-dien-3¦Â-ol C15H22 ÏàËÆ¶È:50% Tetrahedron 2009 65 4035-4043 Terpenoids from the liverwort Chandonanthus hirtellus Yanmei Wang, Leslie J. Harrison, Benito C. Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 13 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2012 20 4954-4961 Design and synthesis of marine fungal phthalide derivatives as PPAR-¦Ã agonists Bin Xiao, Jun Yin, Minhi Park, Juan Liu, Jian Lin Li, Eun La Kim, Jongki Hong, Hae Young Chung, Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 14 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2012 20 4954-4961 Design and synthesis of marine fungal phthalide derivatives as PPAR-¦Ã agonists Bin Xiao, Jun Yin, Minhi Park, Juan Liu, Jian Lin Li, Eun La Kim, Jongki Hong, Hae Young Chung, Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (R,S)-4,5-dihydro-3,3-dipropyl-4-phenyloxycarbonylamino-2(3H)-furanone C17H23NO4 ÏàËÆ¶È:50% Journal of Medicinal Chemistry 2002 45 2824-2831 N-Substituted 4-Amino-3,3-dipropyl-2(3H)-furanones: New Positive Allosteric Modulators of the GABAA Receptor Sharing Electrophysiological Properties with the Anticonvulsant Loreclezole Ahmed El Hadri, Ahmed Abouabdellah, Urs Thomet, Roland Baur, Roman Furtm¨¹ller, Erwin Sigel, Werner Sieghart, and Robert H. Dodd Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 1-(tert-butyldiphenylsilyloxy)-(2S)-2-methyl-nonane C26H40OSi ÏàËÆ¶È:50% Tetrahedron 2013 69 9633-9641 Synthesis of stereopure acyclic 1,5-dimethylalkane chirons: building blocks of highly methyl-branched natural products Original Research Article Nan-Sheng Li, Joseph A. Piccirilli Structure 13C NMR ̼Æ×Ä£Äâͼ |
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