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²éѯ½á¹û£º¹²²éµ½54¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . xuelianlactone ÏàËÆ¶È:66.6% 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:66.6% 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:66.6% Phytochemistry 1989 28 3395-3397 Guaianolides from Saussurea involucrata Li Yu,Jia Zhong-Jian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 8¦Á-hydroxyl-11¦ÂH-11,13-dihydrodehydrocostuslactone ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 5 . dihydroreynosin ÏàËÆ¶È:60% Planta Medica 1988 54 180-181 Sesquiterpene Lactones from Leucanthemopsis pectinata Inds S. Beilido, Manuel Medarde, Esther Caballero, AsunciOn R. Feijo¨®, and Marina Gordaliza Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 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 -------------------------------------------------------------------------------- 7 . 8¦Á-hydroxyl-11¦ÂH-11,13-dihydrodehydrocostuslactone ÏàËÆ¶È:60% China Journal of Chinese Materia Medica 2011 36 1620-1622 Study on chemical constituents from the roots of Saussurea lappa ZHANG, Ting, YANG, Yan, DU, Guanhua, CHEN, Ruoyun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (R)-3-methyl-1-[4-(1-pyrrolidinyl)-2-butynyl]-2-pyrrolidinone C13H20N2O ÏàËÆ¶È:57.1% Journal of Medicinal Chemistry 1993 36 3533-3541 The synthesis and biochemical pharmacology of enantiomerically pure methylated oxotremorine derivatives Eugene J. Trybulski, Jing Zhang, Richard H. Kramss, Richard M. Mangano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (S)-3-methyl-1-[4-(1-pyrrolidinyl)-2-butynyl]-2-pyrrolidinone C13H20N2O ÏàËÆ¶È:57.1% Journal of Medicinal Chemistry 1993 36 3533-3541 The synthesis and biochemical pharmacology of enantiomerically pure methylated oxotremorine derivatives Eugene J. Trybulski, Jing Zhang, Richard H. Kramss, Richard M. Mangano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (11S)-1¦Á-hydroxyeudesm-4(14)-eno-13,6¦Á-lactone C15H22O3 ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 22-30 Guaianolides as Immunomodulators. Synthesis and Biological Activities of Dehydrocostus Lactone, Mokko Lactone, Eremanthin, and Their Derivatives Saori Yuuya, Hisahiro Hagiwara, Toshio Suzuki, Masayoshi Ando, Atsushi Yamada, Kouji Suda, Takao Kataoka, and Kazuo Nagai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 5a C15H24O3 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1998 46 1743-1747 New Guaiane-Type Sesquiterpenoid Glycosides from Torillis japonica Fruit Junichi KITAJIMA,Nobuyuki SUZUKI and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 11¦Â,13-dihydro-1-epireynosin C15H22O3 ÏàËÆ¶È:53.3% Phytochemistry 1993 32 460-462 Sesquiterpene lactones from Artemisia species J. Alberto Marco, Juan F. Sanz, F. Sancenon, A. Rustaiyan, M. Saberi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 14a ÏàËÆ¶È:53.3% Phytochemistry 1989 28 2163-2167 Sesquiterpene lactones from Artemisia hispanica Juan F. Sanz,Oscar Barbera,J.Alberto Marco Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . gallicin C15H22O3 ÏàËÆ¶È:53.3% Journal of the Chemical Society, Perkin Transactions 1 1978 1243-1246 Chemistry of the compositae. Part 38. Structure and absolute configuration of gallicin, a new germacranolide from Artemisia Antonio G. Gonz¨¢lez, Jaime Bermejo, Horacio Mansilla, Antonio Galindo, Juan M. Amaro and Guillermo M. Massanet Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . [(1¦Î),2R,3R]-3-hydroxy-2-(1-hydroxy-2-methyl-2-propenyl)-2-methyl-4-methylideneoctanoic acidmethyl ester C15H27O4 ÏàËÆ¶È:53.3% Tetrahedron 2005 61 6015-6039 Determination of the absolute stereochemistry and asymmetric total synthesis of madindolines A and B: a practical improvement to a second-generation approach from the first-generation Tomoyasu Hirose, Toshiaki Sunazuka, Daisuke Yamamoto, Naoto Kojima, Tatsuya Shirahata, Yoshihiro Harigaya, Isao Kuwajima, Satoshi Ōmura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 3-[3-(4-hydroxy-3-methoxyphenyl)propanoyl]-7-oxa-3-azabicyclo[4.1.0]heptan-2-one ÏàËÆ¶È:53.3% Journal of Chemical Ecology 2008 34 558-574 Inter- and Intraspecific Comparisons of Antiherbivore Defenses in Three Species of Rainforest Understory Shrubs R. M. Fincher, L. A. Dyer, C. D. Dodson, J. L. Richards, M. A. Tobler, J. Searcy, J. E. Mather, A. J. Reid, J. S. Rolig, W. Pidcock Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . deacetyldihydrobuddledin A ÏàËÆ¶È:53.3% Journal of Chinese Medicinal Materials 2009 32 515-517 Studies on Chemical Constituents of Rhizome of Buddleia davidii ZHANG Wen, TANG Sheng-an, DUAN Hong-quan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (3R*,3aR*,7S*,8aS*)-3-isopropyl-3a-methyl-6-methylene-octahydro-2H-spiro[azulene-1,2'-[1,3]dioxolan]-7-ol C17H28O3 ÏàËÆ¶È:52.9% The Journal of Organic Chemistry 2010 75 8337-8350 Construction of the Tricyclic 5−7−6 Scaffold of Fungi-Derived Diterpenoids. Total Synthesis of (¡À)-Heptemerone G and an Approach to Danishefsky¡¯s Intermediate for Guanacastepene A Synthesis Karol Michalak, Michał Michalak, and Jerzy Wicha Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . Isom¨¦re cis (1aR,3aS,5S,7aS) C14H20O4 ÏàËÆ¶È:50% Helvetica Chimica Acta 2001 Vol. 84 2430 Epoxyesters p-menthaniques et pinaniques en milieu basique -Parfum de noix de coco Marie-Jos¨¦phe Bourgeois et Evelyne Montaudon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . salsoline ÏàËÆ¶È:50% Phytochemistry 1991 30 2973-2975 Metabolism of salsolinol by tissue cultures of some Papaveraceae K. Iwasa, M. Kamigauchi, N. Takao Structure 13C NMR ̼Æ×Ä£Äâͼ |
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