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331456351½ð³æ (СÓÐÃûÆø)
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̼Æ× 11.73, 12.17, 18.21, 20.27, 21.34, 29.95, 30.98, 31.94, 33.33, 33.49, 33.68, 37.60, 46.21, 79.07, 93.98, 111.17, 116.12, 117.39, 126.32, 131.63, 132.03, 138.31, 139.10, 158.21, 163.08 ÈܼÁ¼×´¼ лл |
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331456351: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-27 16:20:06
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331456351: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-27 16:20:06
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²éѯ½á¹û£º¹²²éµ½32¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . oxysporidinone ÏàËÆ¶È:75% Journal of Natural Products 2007 70 227-232 Search for Cell Motility and Angiogenesis Inhibitors with Potential Anticancer Activity: Beauvericin and Other Constituents of Two Endophytic Strains of Fusarium oxysporum1 Jixun Zhan, Anna M. Burns, Manping X. Liu, Stanley H. Faeth, and A. A. Leslie Gunatilaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (-)-oxysporidinone ÏàËÆ¶È:75% Fitoterapia 2011 82 777-781 Chemical constituents from endophytic fungus Fusarium oxysporum Quan-Xin Wang,Sai-Fei Li, Feng Zhao, Huan-Qin Dai, Li Bao, Rong Ding, Hao Gao,Li-Xin Zhang, Hua-An Wen, Hong-Wei Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound 1 C28H46NO6 ÏàËÆ¶È:67.8% Fitoterapia 2011 82 777-781 Chemical constituents from endophytic fungus Fusarium oxysporum Quan-Xin Wang,Sai-Fei Li, Feng Zhao, Huan-Qin Dai, Li Bao, Rong Ding, Hao Gao,Li-Xin Zhang, Hua-An Wen, Hong-Wei Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (-)-dimethylsambutoxin C30H43O4N ÏàËÆ¶È:57.6% Bioorganic & Medicinal Chemistry Letters 2011 21 2327-2329 Biomimetic conversion of (-)-fusoxypyridone and (-)-oxysporidinone to (-)-sambutoxin: Further evidence for the structure of the tricyclicpyridone alkaloid, (-)-fusoxypyridone E. M. Kithsiri Wijeratne, A. A. Leslie Gunatilaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 17E-(2-phenyl-2-oxo-1-ethylidene)-5¦Á-androstan-3¦Â-ol C27H36O2 ÏàËÆ¶È:56% Steroids 2011 76 1615-1620 Synthesis and cytotoxicity of 17E-(2-aryl-2-oxo-1-ethylidene)-5¦Á-androstane derivatives Yan Li, Jie Huang, Jinliang Liu, Peiyun Yan, Hui Liu, Qian Sun, Xingbin Wang, Cunde Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (-)-6-deoxyoxysporidinone C28H43NO5 ÏàËÆ¶È:53.5% Journal of Natural Products 2007 70 227-232 Search for Cell Motility and Angiogenesis Inhibitors with Potential Anticancer Activity: Beauvericin and Other Constituents of Two Endophytic Strains of Fusarium oxysporum1 Jixun Zhan, Anna M. Burns, Manping X. Liu, Stanley H. Faeth, and A. A. Leslie Gunatilaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . vitetrifolin C ÏàËÆ¶È:52% Phytochemistry 2000 55 873-877 Diterpenoids from the fruits of Vitex trifolia Masateru Ono, Hiromi Sawamura, Yasuyuki Ito, Koichi Mizuki , Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3-Methoxy-17a-(N-phenylcarboxamido)-13¦Á-D-homoestra-1,3,5(10),17-tetraene C27H31O2N ÏàËÆ¶È:52% Steroids 2010 75 1075-1081 Novel 13¦Â- and 13¦Á-d-homo steroids: 17a-carboxamido-d-homoestra-1,3,5(10),17-tetraene derivatives via palladium-catalyzed aminocarbonylations Attila Tak¨¢cs, P¨¦ter Ács, Zolt¨¢n Berente, J¨¢nos Wölfling, Gyula Schneider, L¨¢szl¨® Koll¨¢r Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 7¦Â,11¦Â-dihydroxy-spongia-13(16),14-diene C20H30O3 ÏàËÆ¶È:52% Tetrahedron 2005 61 1961-1970 Syntheses of oxygenated spongiane diterpenes from carvone. Synthesis of dorisenone C Antonio Abad, Consuelo Agull¨®, Ana C. Cuñat, Ana Bel¨¦n Garc¨ªa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . pentacecilide A C25H32O5 ÏàËÆ¶È:52% The Journal of Antibiotics 2009 62 207-211 Pentacecilides, new inhibitors of lipid droplet formation in mouse macrophages produced by Penicillium cecidicola FKI-3765-1: II. Structure elucidation Hiroyuki Yamazaki, Satoshi mura and Hiroshi Tomoda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (1E,3E,5E,7E)-2-(3,7-dimethyldeca-1,3,5,7,9-pentaenyl)-1,3,3-trimethylcyclohex-1-ene C21H30 ÏàËÆ¶È:52% European Journal of Organic Chemistry 2011 6713-6718 Copper(II)-Mediated Intramolecular Cyclization of (Z)-Chalcogenoenynes: Synthesis of 3-Halochalcogenophene Derivatives Daniela A. Barancelli, Ricardo F. Schumacher, Marlon R. Leite and Gilson Zeni Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . luffarin-N C25H36O4 ÏàËÆ¶È:52% Australian Journal of Chemistry 1992 45 1705-1743 The Luffarins (A-Z), Novel Terpenes From an Australian Marine Sponge, Luffariella geometrica MS Butler and RJ Capon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 17¦Á-(2-Phenyl-1-ethynyl)-5¦Á-androstane-3¦Â,17¦Â-diol C27H36O2 ÏàËÆ¶È:52% Steroids 2011 76 1615-1620 Synthesis and cytotoxicity of 17E-(2-aryl-2-oxo-1-ethylidene)-5¦Á-androstane derivatives Yan Li, Jie Huang, Jinliang Liu, Peiyun Yan, Hui Liu, Qian Sun, Xingbin Wang, Cunde Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 17¦Á-(2-(4-Fluorophenyl)-1-ethynyl)-5¦Á-androstane-3¦Â,17¦Â-diol C27H35FO2 ÏàËÆ¶È:52% Steroids 2011 76 1615-1620 Synthesis and cytotoxicity of 17E-(2-aryl-2-oxo-1-ethylidene)-5¦Á-androstane derivatives Yan Li, Jie Huang, Jinliang Liu, Peiyun Yan, Hui Liu, Qian Sun, Xingbin Wang, Cunde Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . compound 13 ÏàËÆ¶È:52% Australian Journal of Chemistry 1984 37 635-647 The Chemistry of Eremophila spp. XX. The Absolute Stereochemistry of the Viscidane Diterpenes E Ghisalberti, P Jefferies and T Mori Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . salonine-C C28H44N2O ÏàËÆ¶È:51.8% Helvetica Chimica Acta 2004 Vol. 87 439 New Cholinesterase-Inhibiting Steroidal Alkaloids from Sarcococca saligna Atta-ur-Rahman, Zaheer-ul-Haq, Fareeda Feroz, Asaad Khalid, Sarfraz Ahmad Nawaz, M. Riaz Khan, and M. Iqbal Choudhary Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . N-demethylsambutoxin C27H37NO4 ÏàËÆ¶È:51.8% Journal of Natural Products 2006 69(3) 439-442 N-Methyl-4-hydroxy-2-pyridinone Analogues from Fusarium oxysporum Lalith Jayasinghe, Hamed K. Abbas, Melissa R. Jacob,Wimal H. M. W. Herath, and N. P. Dhammika Nanayakkara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 17-(N-Benzamido-carbamoyl)-androst-16-ene C27H36N2O2 ÏàËÆ¶È:51.8% Steroids 2002 67 581-586 Synthesis of steroidal diacyl hydrazines and their 1,3,4-oxadiazole derivatives Zsolt Szarka, Rita Skoda-Földes, Judit Horv¨¢th, Zolt¨¢n Tuba, L¨¢szl¨® Koll¨¢r Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . compound 4 ÏàËÆ¶È:51.8% The Journal of Organic Chemistry 1987 52 5326-5331 New propionate-derived metabolites from Aglaja depicta and from its prey Bulla striata (opisthobranch mollusks) Guido Cimino, Guido Sodano, Aldo Spinella Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 6-epi-oxysporidinone C28H42NO5 ÏàËÆ¶È:50% Journal of Natural Products 2006 69(3) 439-442 N-Methyl-4-hydroxy-2-pyridinone Analogues from Fusarium oxysporum Lalith Jayasinghe, Hamed K. Abbas, Melissa R. Jacob,Wimal H. M. W. Herath, and N. P. Dhammika Nanayakkara Structure 13C NMR ̼Æ×Ä£Äâͼ |
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