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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
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