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²éѯ½á¹û£º¹²²éµ½129¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . brefeldin A ÏàËÆ¶È:72.2% Journal of Asian Natural Products Research 2009 11 54-57 A new compound, brefeldin A formylate, from Penicillium sp. Strain HLKG-44 Han-Wen Zhanga, Hong-Ming Chenga, Hua Fangc, Yu-Fen Zhaoabd and Mei-Juan Fangb Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Brefeldin-A ÏàËÆ¶È:72.2% Magnetic Resonance in Chemistry 2000 38 274-280 NMR structure determination of brefeldin-A, a 13-membered ring fungal metabolite Robert Glaser, Dror Shiftan and Mark Froimowitz Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . brefeldin A ÏàËÆ¶È:72.2% Chinese Pharmaceutical Journal 2010 45 101-103 Water-Soluble Chemical Constituents of Angelica Sinensis(Oliv.) Diels JIANG Wei, WANG Chang-hong, WANG Zheng-tao Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 7-oxobrefeldin A ÏàËÆ¶È:66.6% The Journal of Antibiotics 1987 40 1170-1174 MACROLIDE BIOSYNTHESIS: STEREOCHEMISTRY OF THE HYDROXYLATION OF BREFELDIN C MARIO GONZALEZ DE LA PARRA, C. RICHARD HUTCHINSON Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . brefeldin A ÏàËÆ¶È:66.6% Plant Science 1998 138 67-79 Brefeldin A and ¦Á,¦Â-dehydrocurvularin, two phytotoxins from Alternaria zinniae, a biocontrol agent of Xanthium occidentale Maurizio Vurro, Antonio Evidente, Anna Andolfi, Maria Chiara Zonno, Federico Giordano, Andrea Motta Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . brefeldin A ÏàËÆ¶È:61.1% Planta Medica 1992 58 484 Penicillium camemberti A New Source of Brefeldin A Woif-Rainer Abraham and lians-AdolfArfmann Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . brefeldin A formylate C17H24O5 ÏàËÆ¶È:61.1% Journal of Asian Natural Products Research 2009 11 54-57 A new compound, brefeldin A formylate, from Penicillium sp. Strain HLKG-44 Han-Wen Zhanga, Hong-Ming Chenga, Hua Fangc, Yu-Fen Zhaoabd and Mei-Juan Fangb Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 1b ÏàËÆ¶È:61.1% Tetrahedron Letters 2004 45 199-202 An aldol approach to the total synthesis of (+)-brefeldin A Yikang Wu, Xin Shen, Yong-Qing Yang, Qi Hu, Jia-Hui Huang Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 4-O-acetyl-BFA ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry 2000 8 455-463 Elucidation of strict structural requirements of Brefeldin A as an inducer of differentiation and apoptosis Ji-Wen Zhu, Hideko Nagasawa, Fumi Nagura, Saharuddin B Mohamad, Yoshihiro Uto, Kazuto Ohkura, Hitoshi Hori Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . brefeldin C ÏàËÆ¶È:61.1% The Journal of Antibiotics 1983 36 25-29 BIOSYNTHESIS OF BREFELDIN A INTRODUCTION OF OXYGEN AT THE C-7 POSITION MASAYUKI SUNAGAWA, TOMIHISA OHTA, SHIGEO NOZOE Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (+)-brefeldin C ÏàËÆ¶È:61.1% European Journal of Organic Chemistry 2010 1364-1380 Total Synthesis of (+)-Brefeldin C, (+)-nor-Me Brefeldin A and (+)-4-epi-nor-Me Brefeldin A Sylvie Archambaud, Fr¨¦d¨¦ric Legrand, Karine Aphecetche-Julienne, Sylvain Collet, Andr¨¦ Guingant and M. Evain Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 7'-O-Formylbrefeldin A ÏàËÆ¶È:61.1% Journal of Separation Science 2010 33 277-284 Isolation and purification of macrocyclic components from Penicillium fermentation broth by high-speed counter-current chromatography Xiang Gao, Rongqiang Zhuang, Jiannan Guo, Jian Bao, Meijuan Fang, Yan Liu, Pengxiang Xu and Yufen Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 7'-O-Acetylbrefeldin A ÏàËÆ¶È:61.1% Journal of Separation Science 2010 33 277-284 Isolation and purification of macrocyclic components from Penicillium fermentation broth by high-speed counter-current chromatography Xiang Gao, Rongqiang Zhuang, Jiannan Guo, Jian Bao, Meijuan Fang, Yan Liu, Pengxiang Xu and Yufen Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . scabrolide F C19H24O5 ÏàËÆ¶È:57.8% Journal of Natural Products 2004 67 2079-2082 Scabrolides E−G, Three New Norditerpenoids from the Soft Coral Sinularia scabra Atallah F. Ahmed, Jui-Hsin Su, Yao-Haur Kuo, and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (3aR,3br,4R,9S,14aS,15aS)-4-hydroxy-2,2,9-trimethyl-3a,3b,4,9,10,11,12,14a,15,15a-decahydro-7H-[1,3]dioxolo[4,5]cyclopenta[1,2-f]oxacyclotridecin-7-on C19H28O5 ÏàËÆ¶È:57.8% European Journal of Organic Chemistry 2011 878-891 Syntheses and Biological Properties of Brefeldin Analogues Sebastian Förster, Elke Persch, Olena Tverskoy, Frank Rominger, G¨¹nter Helmchen, Christian Klein, Basak Gönen and Britta Br¨¹gger Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 2¦Â-methoxyclovane-9¦Â,10¦Â-diol C16H26O3 ÏàËÆ¶È:55.5% Journal of Natural Products 2004 67 793-798 Structure−Activity Relationships in the Fungistatic Activity against Botrytis cinerea of Clovanes Modified on Ring C Athina Deligeorgopoulou, Antonio J. Macas-Snchez, Daniel J.Mobbs, Peter B. Hitchcock, James R. Hanson, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 4¦Â,11¦Á-dihydroxy-1-oxoeudesman-6¦Â,12-olide C15H22O5 ÏàËÆ¶È:55.5% Journal of Natural Products 2002 65 1011-1015 Chemical-Microbiological Synthesis of Cryptomeridiol Derivatives by Gliocladium roseum: Semisynthesis of 11-Hydroxyeudesmanolides Andr¨¦s Garc¨ªa-Granados, Mar¨ªa C. Guti¨¦rrez, Andr¨¦s Parra, and Francisco Rivas Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 9¦Â-Trichodiol ÏàËÆ¶È:55.5% Phytochemistry 1993 32 105-116 Revision of the stereochemistry in trichodiol, trichotriol and related compounds, and concerning their role in the biosynthesis of trichothecene mycotoxins Andrew R. Hesketh, Barrie W. Bycroft, Paul M. Dewick, John Gilbert Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 9¦Â-Trichotriol ÏàËÆ¶È:55.5% Phytochemistry 1993 32 105-116 Revision of the stereochemistry in trichodiol, trichotriol and related compounds, and concerning their role in the biosynthesis of trichothecene mycotoxins Andrew R. Hesketh, Barrie W. Bycroft, Paul M. Dewick, John Gilbert Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Brefeldin A ÏàËÆ¶È:55.5% Archives of Pharmacal Research 2008 31 611-616 Cytotoxic activities of trichothecenes isolated from an endophytic fungus belonging to order hypocreales Maneekarn Chinworrungsee, Suthep Wiyakrutta, Nongluksna Sriubolmas, Phitaya Chuailua and Apichart Suksamrarn Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 4-O-methyl-BFA ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2000 8 455-463 Elucidation of strict structural requirements of Brefeldin A as an inducer of differentiation and apoptosis Ji-Wen Zhu, Hideko Nagasawa, Fumi Nagura, Saharuddin B Mohamad, Yoshihiro Uto, Kazuto Ohkura, Hitoshi Hori Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . Peribysin C C15H22O2 ÏàËÆ¶È:55.5% Organic & Biomolecular Chemistry 2004 2 2131-2135 Peribysins A¨CD, potent cell-adhesion inhibitors from a sea hare-derived culture of Periconia species Takeshi Yamada, Masashi Iritani, Katsuhiko Minoura, Kenzo Kawai and Atsushi Numata Structure 13C NMR ̼Æ×Ä£Äâͼ |
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