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²éѯ½á¹û£º¹²²éµ½2008¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . mairetolide F C15H22O4 ÏàËÆ¶È:86.6% Journal of Natural Products 2006 69 1471-1475 Eremophilanes from Senecio mairetianus and Some Reaction Products Ana-L. Prez-Castorena, Amira Arciniegas, S. Laura Guzmn, Jos Luis Villaseor, and Alfonso Romo de Vivar Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . mairetolide G C15H22O5 ÏàËÆ¶È:86.6% Journal of Natural Products 2006 69 1471-1475 Eremophilanes from Senecio mairetianus and Some Reaction Products Ana-L. Prez-Castorena, Amira Arciniegas, S. Laura Guzmn, Jos Luis Villaseor, and Alfonso Romo de Vivar Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . mairetolide H C15H22O5 ÏàËÆ¶È:80% Journal of Natural Products 2006 69 1471-1475 Eremophilanes from Senecio mairetianus and Some Reaction Products Ana-L. Prez-Castorena, Amira Arciniegas, S. Laura Guzmn, Jos Luis Villaseor, and Alfonso Romo de Vivar Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Herticin A C15H22O3 ÏàËÆ¶È:80% Helvetica Chimica Acta 2009 92 404-408 Herticins A and B, New Sesquiterpenes from Hertia intermedia Shazia Yasmeen, Naheed Riaz, Amna Bibi, Nighat Afza, Abdul Malik, Rasool Bukhsh Tareen Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . atractylenolide I ÏàËÆ¶È:80% Natural Product Research 2008 22 1418-1427 Anti-inflammatory components isolated from Atractylodes macrocephala Koidz Haiyan Dong; Langchong He; Meng Huang; Yalin Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 10¦Â-hydroxyeremophilenolide C15H22O3 ÏàËÆ¶È:80% Phytochemistry 1990 29 2207-2210 Eremophilenolides from Hertia cheirifolia Georges Massiot,Jean-Marc Nuzillard,Louisette Le Men-Olivier,Paul Aclinou,Abdelhamid Benkouider,Abdessemed Khelifa Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . atractylenolide I ÏàËÆ¶È:80% Chinese Pharmaceutical Journal 2007 42 1055-1059 Studies on Constituents and Anti-Inflammatory Activity of Rhizoma Atractylodis macrocephalae DONG Hai-yan, DONG Ya-lin, HE Lang-chong, PEI Wei-jing Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (4aS,8aR,9aS)-3,8a-dimethyl-5-methylidene-4a,5,6,7,8,8a,9,9a-octahydronaphtho[2,3-b]furan-2(4H)-one ÏàËÆ¶È:80% Russian Journal of Organic Chemistry 2010 46 1719-1734 Synthetic transformations of methylenelactones of eudesmanic type. Behavior of isoalantolactone under the conitions of heck reaction A. V. Belovodskii, E. E. Shults, M. M. Shakirov, I. Yu. Bagryanskaya and Yu. V. Gatilov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . atractylenolide I ÏàËÆ¶È:80% Journal of Ethnopharmacology 2007 114 212-217 Screening for the anti-inflammatory activity of fractions and compounds from Atractylodes macrocephala koidz Cui-Qin Li, Lang-Chong He, Hai-Yan Dong, Ju-Qing Jin Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . atractylenolide I ÏàËÆ¶È:80% China Journal of Chinese Materia Medica 2011 36 578-581 Chemical constituents from aerial part of Atractylodes macrocephala PENG Wei, HAN Ting, LIU Qingchun, QIN Luping Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . asterolid ÏàËÆ¶È:80% Acta Chimica Sinica 1999 57 1022-1025 Structural Elucidation of Biepiasterolid WANG Bao-De YU Yi-Hua TENG Ning-Ning JIANG Shan-Hao ZHU Da-Yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Atractylenolide II [eudesma-4(15),7(11)-dien-8¦Á,12-olide] C15H20O3 ÏàËÆ¶È:80% Journal of Asian Natural Products Research 2013 15 344-356 Four new eudesmane-type sesquiterpenoid lactones from atractylenolide II by biotransformation of rat hepatic microsomes Ying Li, Jing Liu & Xiu-Wei Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (+)-(5R,7S,9R,10S)-2-oxocadinan-3,6(11)-dien-12,7-olide C15H18O3 ÏàËÆ¶È:73.3% Journal of Natural Products 2008 71(8) 1485-1488 Cadinane Sesquiterpenes from the Leaves of Eupatorium adenophorum Lan He, Jing Hou, Maoluo Gan, Jiangong Shi, Suchada Chantrapromma,Hoong-Kun Fun, Ian D. Williams, and Herman H.-Y. Sung Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . mairetolide F C15H22O4 ÏàËÆ¶È:73.3% Journal of Natural Products 2010 73 683-687 Eremophilane-Type Sesquiterpenes from the Fungus Xylaria sp. BCC 21097 Masahiko Isaka, Panida Chinthanom, Tanapong Boonruangprapa, Nattawut Rungjindamai and Umpava Pinruan Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (3R)-3-hydroxyatractylenolide III C15H20O4 ÏàËÆ¶È:73.3% Chemistry & Biodiversity 2010 7 151-157 Sesquiterpenoids and Diterpenoids from Chloranthus anhuiensis Yong-Jiang Xu, Chun-Ping Tang, Min-Jia Tan, Chang-Qiang Ke, Tao Wu and Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 4¦Á-Hydroxy-5¦Á,8¦Á(H)-eudesm-7(11)-en-8,12-olide C15H22O3 ÏàËÆ¶È:73.3% Helvetica Chimica Acta 2010 93 803-810 Terpenoids from Roots of Chloranthus spicatus Zhi-Yong Xiao, Xia-Chang Wang, Gui-Ping Zhang, Zhong-Liang Huang and Li-Hong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . dysidamide D C15H22NO3Cl5 ÏàËÆ¶È:73.3% Tetrahedron 2005 61 955-963 New polychlorinated pyrrolidinones from the Red Sea marine sponge Lamellodysidea herbacea Pierre Sauleau, Pascal Retailleau, Jean Vacelet, Marie-Lise Bourguet-Kondracki Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 8-epiasterolid ÏàËÆ¶È:73.3% Acta Chimica Sinica 1999 57 1022-1025 Structural Elucidation of Biepiasterolid WANG Bao-De YU Yi-Hua TENG Ning-Ning JIANG Shan-Hao ZHU Da-Yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 10¦Â-hydroxy-eremophilen-7(11)-en-12,8¦Á-olide ÏàËÆ¶È:73.3% Chinese Traditional and Herbal Drugs 2012 43 1270-1272 Chemical constituents of Ligularia intermedia from Henan Province YUAN Yong-liang; YE Dan-dan; LIANG Hui-juan; LIU Wei; BAI Su-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . mairetolide E C16H24O4 ÏàËÆ¶È:68.7% Journal of Natural Products 2006 69 1471-1475 Eremophilanes from Senecio mairetianus and Some Reaction Products Ana-L. Prez-Castorena, Amira Arciniegas, S. Laura Guzmn, Jos Luis Villaseor, and Alfonso Romo de Vivar Structure 13C NMR ̼Æ×Ä£Äâͼ |
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