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xifangchenquгæ (СÓÐÃûÆø)
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΢Æ×ÇóÖú86-1A ÒÑÓÐ1È˲ÎÓë
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| 13C-NMR:10.53,14.68,15.46,15.69,16.33,21.07,23.97,28.84,29.83,33.83,35.08,39.26,40.48,49.11,49.71,66.56,76.64,121.50,124.46,129.03,133.07,136.68,138.37,146.73,147.29,171.05,207.90 |
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- ×¢²á: 2011-12-14
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xifangchenqu: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-28 17:41:22
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xifangchenqu: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-28 17:41:22
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1 . Fusaproliferin ÏàËÆ¶È:100% Bioscience, Biotechnology, and Biochemistry 2003 66 685-688 Phytotoxic Sesterterpene, 11-Epiterpestacin, from Bipolaris sorokiniana NSDR-011 Yoichiro NIHASHI, Chi-Hwan LIM, Chihiro TANAKA, Hisashi MIYAGAWA and Tamio UENO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . fusaproliferin C27H40O5 ÏàËÆ¶È:100% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 120-123 Study on Secondary Metabolites of Endophytic Fungal Strain Botryosphaeria sp.MHF of Maytenus hookeri YUAN Lin, SHEN Fang, MA Yin-hai, CHEN Xiao-ni, HUANG Xing-nan, GU Xue-zhu, KANG Wen-yi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . fusaproliferin C27H40O5 ÏàËÆ¶È:96.2% Journal of Natural Products 1996 59 109-112 Structure and Absolute Stereochemistry of Fusaproliferin, a Toxic Metabolite from Fusarium proliferatum Antonello Santini, Alberto Ritieni, Vincenzo Fogliano, Giacomino Randazzo, Luisa Mannina, Antonio Logrieco, and Ettore Benedetti Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . fusaproliferin C27H40O5 ÏàËÆ¶È:96.2% Natural Toxins 1995 3 17-20 Isolation and characterization of fusaproliferin, a new toxic metabolite from Fusarium proliferatum Alberto Ritieni, Vincenzo Fogliano, Giacomino Randazzo, Angela Scarallo, Antonio Logrieco, Antonio Moretti, Luisa Manndina and Antonio Bottalico Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 11-Epiterpestacin ÏàËÆ¶È:88.8% Bioscience, Biotechnology, and Biochemistry 2003 66 685-688 Phytotoxic Sesterterpene, 11-Epiterpestacin, from Bipolaris sorokiniana NSDR-011 Yoichiro NIHASHI, Chi-Hwan LIM, Chihiro TANAKA, Hisashi MIYAGAWA and Tamio UENO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (-)-Terpestacin C25H38O4 ÏàËÆ¶È:85.1% Journal of Basic Microbiology 2001 41 179-183 (¨C)-Terpestacin and L-tenuazonic acid, inducers of pigment and aerial mycelium formation by Fusarium culmorum JP 15 Brigitte Schlegel, Michaela Schmidtke, Heinrich Dörfelt, Peter Kleinwächter and Udo Gräfe Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . fusaprolifin B C27H38O5 ÏàËÆ¶È:81.4% Helvetica Chimica Acta 2013 96 437-444 Sesterterpenes and 2H-Pyran-2-ones (=¦Á-Pyrones) from the Mangrove-Derived Endophytic Fungus Fusarium proliferatum MA-84 Dong Liu, Xiao-Ming Li, Chun-Shun Li and Bin-Gui Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 52 C27H40O3 ÏàËÆ¶È:77.7% Chemistry-A European Journal 2010 16 6265-6277 Cyclic 1,2-Diketones as Core Building Blocks: A Strategy for the Total Synthesis of (− -TerpestacinBarry M. Trost, Guangbin Dong and Jennifer A. Vance Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . fusaprolifin A C27H38O5 ÏàËÆ¶È:77.7% Helvetica Chimica Acta 2013 96 437-444 Sesterterpenes and 2H-Pyran-2-ones (=¦Á-Pyrones) from the Mangrove-Derived Endophytic Fungus Fusarium proliferatum MA-84 Dong Liu, Xiao-Ming Li, Chun-Shun Li and Bin-Gui Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . terpestacin triacetate ÏàËÆ¶È:74.1% The Journal of Antibiotics 1993 46 367-373 TERPESTACIN, A NEW SYNCYTIUM FORMATION INHIBITOR FROM Arthrinium sp. MASAHISA OKA, SEIJI IIMURA, OSAMU TENMYO, YOSUKE SAWADA, MASARU SUGAWARA, NORIYUKI OHKUSA, HARUAKI YAMAMOTO, KIMIO KAWANO, SHIU-LOK HU, YASUO FUKAGAWA, TOSHIKAZU OKI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . sesterterpenoic acid C25H40O3 ÏàËÆ¶È:74.0% Journal of Natural Products 2002 65 1749-1753 Isolation and Structure Elucidation of an Isoflavone and a Sesterterpenoic Acid from Henriettella fascicularis Angela I. Calder¨®n,Christian Terreaux, Kurt Schenk,Phil Pattison, Joanna E. Burdette,John M. Pezzuto, Mahabir P. Gupta,and K. Hostettmann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 1 C27H42O4 ÏàËÆ¶È:74.0% Phytochemistry 1982 21 421-424 A quinone-hydroquinone couple from the Brown alga Cystoseira stricta Vincenzo Amico, Giovanna Oriente, Mario Piattelli, Giuseppe Ruberto, Corrado Tringali Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . terpestacin C25H38O4 ÏàËÆ¶È:74.0% The Journal of Antibiotics 1993 46 367-373 TERPESTACIN, A NEW SYNCYTIUM FORMATION INHIBITOR FROM Arthrinium sp. MASAHISA OKA, SEIJI IIMURA, OSAMU TENMYO, YOSUKE SAWADA, MASARU SUGAWARA, NORIYUKI OHKUSA, HARUAKI YAMAMOTO, KIMIO KAWANO, SHIU-LOK HU, YASUO FUKAGAWA, TOSHIKAZU OKI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 3-((2-(2-ethyl-4-(5-(3-ethyl-5,5-dimethyl-4,5,6,7-tetrahydrobenzo[c]thiophen-1-yl)-1,2,4-oxadiazol-3-yl)-6-methylphenoxy)ethyl)amino)propanoic acid ÏàËÆ¶È:74.0% Journal of Medicinal Chemistry 2014 57 78-97 Novel S1P1 Receptor Agonists - Part 2: From Bicyclo[3.1.0]hexane-Fused Thiophenes to Isobutyl Substituted Thiophenes Martin H. Bolli, Jörg Velker, Claus M¨¹ller, Boris Mathys, Magdalena Birker, Roberto Bravo, Daniel Bur, Ruben de Kanter, Patrick Hess, Christopher Kohl, David Lehmann, Solange Meyer, Oliver Nayler, Markus Rey, Michael Scherz, and Beat Steiner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . negundonorin B C29H42O2 ÏàËÆ¶È:72.4% Fitoterapia 2012 83 49-54 Sesquiterpenoids and norterpenoids from Vitex negundo Cheng-Jian Zheng, Jiang Pu, Hong Zhang, Ting Han, Khalid Rahman, Lu-Ping Qin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 55 C25H36O3 ÏàËÆ¶È:71.8% Chemistry-A European Journal 2010 16 6265-6277 Cyclic 1,2-Diketones as Core Building Blocks: A Strategy for the Total Synthesis of (− -TerpestacinBarry M. Trost, Guangbin Dong and Jennifer A. Vance Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . (2R)-9'-oxo-¦Ä-tocotrienol C27H38O3 ÏàËÆ¶È:70.3% Chemical & Pharmaceutical Bulletin 2008 56(1) 124-128 New Chromane Derivatives Isolated from the Brown Alga, Sargassum micracanthum Makoto IWASHIMA,Natsuko TAKO,Tomoyo HAYAKAWA,Takayuki MATSUNAGA,Jun MORI,d and Haruo SAITO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . chabrolobenzoquinone C C27H36O4 ÏàËÆ¶È:70.3% Journal of Natural Products 2004 67 2048-2052 Novel Meroditerpenoid-Related Metabolites from the Formosan Soft Coral Nephthea chabrolii Jyh-Horng Sheu, Jui-Hsin Su, Ping-Jyun Sung, Guey-Horng Wang, and Chang-Feng Dai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . trans-epothilone C1 C25H37NO5S ÏàËÆ¶È:70.3% Journal of Natural Products 2001 64 847-856 New Natural Epothilones from Sorangium cellulosum, Strains So ce90/B2 and So ce90/D13: Isolation, Structure Elucidation, and SAR Studies Ingo H. Hardt,Heinrich Steinmetz, Klaus Gerth, F. Sasse, Hans Reichenbach, and Gerhard Höfle Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . fallachromenoic acid C27H35ClO4 ÏàËÆ¶È:70.3% Phytochemistry 2009 70 250-255 Meroditerpenoids from the southern Australian marine brown alga Sargassum fallax Priyanka Reddy, Sylvia Urban Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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