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¶¹¸ç: ½ð±Ò+4, лл 2012-09-02 08:32:55
zhangli1987: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-10-11 23:42:15
¶¹¸ç: ½ð±Ò+4, лл 2012-09-02 08:32:55
zhangli1987: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-10-11 23:42:15
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²éѯ½á¹û£º¹²²éµ½17¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . xuelianlactone ÏàËÆ¶È:60% China Journal of Chinese Materia Medica 2008 33 1032-1035 Studies on chemical constituents of Saussurea laniceps DAWA Zhuoma, ZHOU Yan, BAI Yang, GESANG Suolang, XIE Ping, DING Lisheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 8¦Á-hydroxyl-11¦ÂH-11,13-dihydrodehydrocostuslactone ÏàËÆ¶È:60% Fitoterapia 2011 82 983-987 Sesquiterpene lactones from Saussurea involucrata Wan Xiao, Xian Li, Ning Li, Makabili Bolati, Xinjun Wang, Xiaoguang Jia, Yuqing Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 8¦Á-hydroxy-11¦ÂH-11,13-dihydrodehydrocostuslactone C15H20O3 ÏàËÆ¶È:60% Phytochemistry 1989 28 3395-3397 Guaianolides from Saussurea involucrata Li Yu,Jia Zhong-Jian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . involucrato lactone ÏàËÆ¶È:60% Journal of Shenyang Pharmaceutical University 2011 28 120-123 Isolation and identification of chemical constituents from whole plant of Saussurea involucrata Kar. et kir. HOU Peng-yi, HUANG Jian, SUN Bo-hang, WU Li-jun, GAO Hui-yuan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 8¦Á-hydroxyl-11¦ÂH-11,13-dihydrodehydrocostuslactone ÏàËÆ¶È:60% Journal of Integrative Plant Biology 2007 49 609-614 Two New Sesquiterpenoid Glucosides from the Aerial Parts of Saussurea involucrate Xiao-Ling Wang, Suo-Lang Gesang, Wei Jiao, Xun Liao and Li-Sheng Ding* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . halenin A C15H20O5 ÏàËÆ¶È:60% Journal of Chemical Research 2002 26 368-369 Two new sesquiterpenes from the Chinese herb Halenia elliptica and their antibacterial and antitumour activity Dai, Jingqiu; Shi, Yanping; Zhao, Chenyang; Yang, Li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 1¦Á,5¦Â-dihydroxyeudesm-4(15)-en-6¦Â,11¦ÂH-12,6-olide ÏàËÆ¶È:53.3% Phytochemistry 1994 37 477-485 Sesquiterpene lactones from North African Artemisia species J.Alberto Marco, Juan F. Sanz-Cervera, Jose M. Pareja, Felix Sancenon, Joan Valles-Xirau Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . elemanolide ÏàËÆ¶È:53.3% Phytochemistry 1991 30 2331-2333 Sesquiterpene lactones and flavonoids from Centaurea aspera M.Luz Cardona, Isabel Fern¨¢ndez, Jos¨¦ R. Pedro, Beatriz P¨¦rez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . japonicolactone ÏàËÆ¶È:53.3% Fitoterapia 2011 82 983-987 Sesquiterpene lactones from Saussurea involucrata Wan Xiao, Xian Li, Ning Li, Makabili Bolati, Xinjun Wang, Xiaoguang Jia, Yuqing Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . silylether ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry Letters 2004 14 4931-4934 Synthesis and evaluation of 4-(1-aminoalkyl)-N-(4-pyridyl)cyclohexanecarboxamides as Rho kinase inhibitors and neurite outgrowth promoters Karine Gingras, Hovsep Avedissian, Eryk Thouin, V¨¦ronique Boulanger, Charles Essagian, Lisa McKerracher, William D. Lubell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (E,E)-11-Hydroperoxy-3,7,1l-trimethyl-1,6,9-dodecotrien-3,5-diol ÏàËÆ¶È:53.3% Phytochemistry 1985 24 1729-1733 Oxygenated nerolidol derivatives from Artemisia alba Giovanni Appendino, Pierluigi Gariboldi, Francesco Menichini Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (E,E)-3,7,11-Trimethyl-1,6,9-dodecatriene-3,5,11-triol ÏàËÆ¶È:53.3% Phytochemistry 1985 24 1729-1733 Oxygenated nerolidol derivatives from Artemisia alba Giovanni Appendino, Pierluigi Gariboldi, Francesco Menichini Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . tsugicoline A1 C15H23NO4 ÏàËÆ¶È:53.3% Journal of the Chemical Society, Perkin Transactions 1 2000 745-751 Secondary mould metabolites. Part 58. Modifications in basic conditions and Michael additions of the protoilludane sesquiterpene tsugicoline A; some implications for the biogenesis of other sesquiterpenoids produced by Basidiomycetes Alberto Arnone, Cristiana De Gregorio, Andrea Mele, Gianluca Nasini and Orso Vajna de Pava Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 3¦Á,8¦Á-dihydroxy,11¦ÂH-11,13-dihydrodehydrocotuslactone ÏàËÆ¶È:53.3% Journal of Integrative Plant Biology 2007 49 609-614 Two New Sesquiterpenoid Glucosides from the Aerial Parts of Saussurea involucrate Xiao-Ling Wang, Suo-Lang Gesang, Wei Jiao, Xun Liao and Li-Sheng Ding* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . japonicolactone ÏàËÆ¶È:53.3% Acta Chimica Sinica 1991 49 1136-1141 The Structures of a Guaianolide and Its Glucoside Jia Zhong-Jian Li Yu Shi Jian-Gong ; Wang Qi-Guang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . conocenol C C16H26O3 ÏàËÆ¶È:50% Journal of Natural Products 2007 70 1503-1506 Sesquiterpenes from Cultures of the Basidiomycete Conocybe siliginea Dong-Ze Liu,Fei Wang, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Methyl-(1S,4S,5S,9R,11S)-4,5-epoxycaryophyllen-13-oate C16H24O3 ÏàËÆ¶È:50% Bulletin of the Chemical Society of Japan 2006 79 1547-1551 New ¦Â-Caryophyllene-Derived Terpenoids from the Formosan Soft Coral Sinularia gibberosa Shin-Pin Chen, Chih-Hua Chao, Ho-Cheng Huang, Yang-Chang Wu, Chung-Kuang Lu, Chang-Feng Dai, Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |

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