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[ÇóÖú] ΢Æ×ÇóÖú86-1A ÒÑÓÐ1È˲ÎÓë

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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xifangchenqu: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-28 17:41:22
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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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 (−-Terpestacin
Barry M. Trost, Guangbin Dong and Jennifer A. Vance
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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 (−-Terpestacin
Barry M. Trost, Guangbin Dong and Jennifer A. Vance
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ
2Â¥2015-03-28 06:33:34
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