| ²é¿´: 233 | »Ø¸´: 1 | ||||
panxiaolinÒø³æ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú΢Æ×
|
| ´òÆ×ÈܼÁ ßÁà¤17.1,17.7,23.0,26.2,26.9,27.1,27.6,29.6,29.8,29.8,29.9,30.1,31.4,32.1,35.9,36.3,48.3,51.7,54.8,71.1,126.3,130.3 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
070300»¯Ñ§Ñ§Ë¶311·ÖÇóµ÷¼Á
ÒѾÓÐ15È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ13È˻ظ´
²ÄÁÏÓ뻯¹¤×¨Ë¶306·ÖÕÒºÏÊʵ÷¼Á
ÒѾÓÐ19È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ19È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ22È˻ظ´
298Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
368»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
326Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½1248¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (Z)-2-butyroxy-8-heptadecene ÏàËÆ¶È:68.1% Journal of Chemical Ecology 2009 35 715-723 (2S,8Z)-2-Butyroxy-8-heptadecene: Major Component of the Sex Pheromone of Chrysanthemum Gall Midge, Rhopalomyia longicauda Ya-Jia Liu, David Hall, Jerry Cross, Dudley Farman, Lakmali Amarawardana, Qing-Ran Liu, Xiong-Kui He Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 5,5'-trans-cyclohexane-1,4-diyl 1,1'-didecyl bis(N-hept-6-ynoyl-L-glutamate) C50H82N2O10 ÏàËÆ¶È:65.2% European Journal of Organic Chemistry 2011 2247-2255 Synthesis, Gelation Properties and Photopolymerization of Macrocyclic Diacetylenedicarboxamides Derived from L-Glutamic Acid and trans-1,4-Cyclohexanediol Jun'ichi Nagasawa, Masaru Yoshida and Nobuyuki Tamaoki Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1-O-[(11Z)-octadecenyl]-sn-glyceryl-3-phosphorylcholine ÏàËÆ¶È:63.6% Journal of Natural Products 1994 Vol 57 84 Polar Metabolites from the Sea Cucumber Cucumaria frondosa Nurettin Yayli, John A. Findlay Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 6Z,8Z-Heneicosadien-11-ol ÏàËÆ¶È:63.6% Tetrahedron Letters 2004 45 7651-7654 Stereospecific synthesis of all four isomeric 6,8-heneicosadien-11-ones: sex pheromone components of the painted apple moth Teia anartoides Daniel J. Comeskey, Barry J. Bunn, Simon Fielder Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (2R) 2-{[trans-2-(Octanoylamino)cyclopropyl]methoxy}-propionyl-L-alanyl-D-isoglutamine C23H40N4O7 ÏàËÆ¶È:63.6% Zeitschrift f¨¹r Naturforschung B 2003 58 1247-1254 Synthesis of Spacered Cyclopropanoid Muramyldipeptide Analogues as Potential Immunostimulants R. Csuk and G. Göthe Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . acetylleptophyllin A C20H39NO4 ÏàËÆ¶È:63.6% Tetrahedron 1995 51 5929-5934 Bioactive and other piperidine alkaloids from Cassia leptophylla Vanderlan da S. Bolzani, A.A. Leslie Gunatilaka, David G.I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1,4-dideoxy-5-O-[(9Z)-octadec-9-en-1-yl]-1,4-imino-D-ribitol C23H45NO3 ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry 2011 19 7720-7727 Anti-cancer activity of 5-O-alkyl 1,4-imino-1,4-dideoxyribitols Claudia Bello, Giovanna Dal Bello, Michele Cea, Aimable Nahimana, Dominique Aubry, Anna Garuti, Giulia Motta, Eva Moran, Floriana Fruscione, Paolo Pronzato, Francesco Grossi, Franco Patrone, Alberto Ballestrero, Marc Dupuis, Bernard Sordat, Kaspar Zimmermann, Jacqueline Loretan, Markus Wartmann, Michel A. Duchosal, Alessio Nencioni, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (Z)-1-iodononadec-10-en-2-ol ÏàËÆ¶È:63.6% Tetrahedron 2012 68 2973-2983 Synthesis of (Z)-(2'R)-1-O-(2'-methoxynonadec-10'-enyl)-sn-glycerol, a new analog of bioactive ether lipids Ren¨¦ Pemha, Dieudonn¨¦ Emmanuel Pegnyemb, Paul Mosset Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (6Z,13R)-methylheneicosene ÏàËÆ¶È:63.6% Journal of Chemical Ecology 2000 26 1135-1149 Major Sex Pheromone Component of Female Herald Moth Scoliopteryx libatrix is the Novel Branched Alkene (6Z,13)-Methylheneicosene W. Francke, E. Plass, N. Zimmermann, H. Tietgen, T. Tolasch, S. Franke, M. Subchev, T. Toshova, J. A. Pickett, L. J. Wadhams, C. M. Woodcock Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 15 C23H37NO ÏàËÆ¶È:63.6% Journal of the American Chemical Society 1994 116 11241-11250 Enantioselective Total Synthesis of Either Enantiomer of the Antifungal Antibiotic Preussin (L-657,398) from (S)-Phenylalanine Wei Deng, Larry E. Overman Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . juliprosopine ÏàËÆ¶È:62.5% Journal of Natural Products 2009 72 92-98 Indolizidine, Antiinfective and Antiparasitic Compounds from Prosopis glandulosa var. glandulosa Volodymyr Samoylenko, Mohammad K. Ashfaq, Melissa R.Jacob,Babu L. Tekwani, Shabana I. Khan, Susan P. Manly,Vaishali C. Joshi, Larry A.Walker,and Ilias Muhammad Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 5,5'-trans-cyclohexane-1,4-diyl 1,1'-didecyl bis(N-non-8-ynoyl-L-glutamate) C54H90N2O10 ÏàËÆ¶È:61.5% European Journal of Organic Chemistry 2011 2247-2255 Synthesis, Gelation Properties and Photopolymerization of Macrocyclic Diacetylenedicarboxamides Derived from L-Glutamic Acid and trans-1,4-Cyclohexanediol Jun'ichi Nagasawa, Masaru Yoshida and Nobuyuki Tamaoki Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (Z)-N-{(1S)-2-hydroxy-1-[[4-(2-diazoacetyl)phenyl]methyl]-etil}-9-octadecenamide C29H45N3O3 ÏàËÆ¶È:61.5% Journal of Medicinal Chemistry 2006 49 2320-2332 Development of the First Potential Covalent Inhibitors of Anandamide Cellular Uptake Aniello Schiano Moriello, Laurence Balas, Alessia Ligresti, Maria Grazia Cascio, Thierry Durand, Enrico Morera, Giorgio Ortar, and Vincenzo Di Marzo Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . plakinic acid M C26H42O4 ÏàËÆ¶È:60.8% Organic Letters 2010 Vol.12,No.7 1524-1527 Liposomal Circular Dichroism.Assignment of Remote Stereocenters in Plakinic Acids K and L from a Plakortis-Xestospongia Sponge Association Doralyn S. Dalisay, Tim Quach, and Tadeusz F. Molinski Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Compound(2S,3R,5S)-19 ÏàËÆ¶È:60.8% Bioorganic & Medicinal Chemistry 2008 16 950-964 RCAI-8, 9, 18, 19, and 49¨C52, conformationally restricted analogues of KRN7000 with an azetidine or a pyrrolidine ring:Their synthesis and bioactivity for mouse natural killer T cells to produce cytokines Ken-ichi Fuhshuku,Naomi Hongo,Takuya Tashiro,Yui Masuda,Ryusuke Nakagawa,Ken-ichiro Seino,Masaru Taniguchi and Kenji Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 17-Hydroxy-16¦Â-(4-(methoxycarbonyl)-1,2,3-triazol-1-yl)-5-androstane C23H35N3O3 ÏàËÆ¶È:60.8% Steroids 2012 77 738-744 Synthesis of ferrocene-labeled steroids via copper-catalyzed azide¨Calkyne cycloaddition. Reactivity difference between 2¦Â-, 6¦Â- and 16¦Â-azido-androstanes Klaudia Feh¨¦r, J¨¢nos Balogh, Zsolt Cs¨®k, Tam¨¢s K¨¦gl, L¨¢szl¨® Koll¨¢r, Rita Skoda-Földes Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-08-02 10:32:34














»Ø¸´´ËÂ¥
100