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°´´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 10.63,14.56,15.53,15.77,16.43,24.04,29.02,29.98,35.12,37.29,39.50,40.54,49.19,49.80,66.30,76.71,121.76,124.55,129.18,133.09,136.65,138.24,146.93,149.34,208.24 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½64¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 11-Epiterpestacin 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (-)-Terpestacin C25H38O4 ÏàËÆ¶È:96% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . fusaproliferin C27H40O5 ÏàËÆ¶È:88.4% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . fusaproliferin C27H40O5 ÏàËÆ¶È:88.4% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Fusaproliferin ÏàËÆ¶È:85.1% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . terpestacin C25H38O4 ÏàËÆ¶È:72% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . longithorone J C21H30O2 ÏàËÆ¶È:56% Journal of Natural Products 1999 62 158-160 Longithorones J and K, Two New Cyclofarnesylated Quinone Derived Metabolites from the Australian Ascidian Aplidium longithorax Rohan A. Davis, Anthony R. Carroll, and Ronald J. Quinn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3-epi-telocinobufagin C24H34O5 ÏàËÆ¶È:56% Chinese Chemical Letters 2007 18 1316-1318 Two new compounds derived from bufalin Jun Zhao , Shu Hong Guan , Xiao Bin Chen, Wei Wang, Min Ye, De An Guo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . beauveriolide III C27H41N3O5 ÏàËÆ¶È:56% The Journal of Antibiotics 1999 52 7-12 Structure Elucidation of Fungal Beauveriolide III, a Novel Inhibitor of Lipid Droplet Formation in Mouse Macrophages ICHIJI NAMATAME, HIROSHI TOMODA, NORIKO TABATA, SHUYI SI, SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . hydroquinone ÏàËÆ¶È:55.5% Journal of Natural Products 2004 67 1295-1302 Chemical Investigation of Predator-Deterred Macroalgae from the Antarctic Peninsula Sridevi Ankisetty, Santhisree Nandiraju, Hla Win, Young Chul Park, Charles D. Amsler, James B. McClintock, Jill A. Baker, Thushara K. Diyabalanage, Albert Pasaribu, Maya P. Singh, William M. Maiese, Rosa D. Walsh, Michael J. Zaworotko, and Bill J. Baker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . N20-acetylbuxamine G C27H44N2O ÏàËÆ¶È:55.5% Phytochemistry 2000 54 951-957 Four steroidal alkaloids from the leaves of Buxus sempervirens Fabrice Loru, Dani¨¦le Duval, Andr¨¦Aumelas, Fatima Akeb, Didier Gu¨¦don, Roger Guedj Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . fusaprolifin B C27H38O5 ÏàËÆ¶È:55.5% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 2¦Â-hydroxy-15-phenyl-(22,25-dihydroxy)-ent-labda-8(17),13(E)-diene ÏàËÆ¶È:53.8% Molecules 2009 14 2181-2194 Synthesis of Two New Hemisynthetic Diterpenylhydroquinones from Natural Ent-Labdanes Luis Espinoza Catal¨¢n, Karen Catal¨¢n Mar¨ªn, Alejandro Madrid Villegas, H¨¦ctor Carrasco Altamirano, Joan Villena Garc¨ªa and Mauricio Cuellar Fritis Structure 13C NMR ̼Æ×Ä£Äâͼ |

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