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11.7,12.5,13.6,17.5,21.2,21.5,22.2,23.8,25.1,26.2,26.5,35.5,36.5,37.5,37.7,60.5,72.1,83.7,85.5,107.1,108.3,135.2,140.1,144.0,153.3,170.8,198.6
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

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̼Æ×¿â£º   Nat Syn


²éѯ½á¹û£º¹²²éµ½145¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     compound 4
C30H44O8     ÏàËÆ¶È:90%
Bioscience, Biotechnology, and Biochemistry          1994          58          1143-1145
Phytotoxins Produced by the Plant Pathogenic Fungus Bipolaris bicolor El-1
Hisashi Miyagawa, Shinji Nagai, Tetsu Tsurushima, Mamoru Sato, Tamio Ueno, Hiroshi Fukami
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Isocochlioquinone B
C30H42O8     ÏàËÆ¶È:86.6%
Journal of Asian Natural Products Research          2011          Vol.13,No.8          761-764
Neuraminidase inhibitory terpenes from endophytic Cochliobolus sp.
Gao-Fei Zhang, Zhi-Kai Guo, Wei Wang, Jiang-Tao Cui,Ren-Xiang Tan and Hui-Ming Ge
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     isocochlioquinone A
    ÏàËÆ¶È:83.3%
Chemistry of Natural Compounds          2015          51          270−272
Chemical Constituents of the Fungus Veronaea sp.
Liang Zhou, Xi Zheng, Chun-Ping Wan, Ze-Fen Yu, Ke-Qin Zhang, Guo-Hong Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     stemphone G
C30H42O9     ÏàËÆ¶È:68.9%
The Journal of Antibiotics          2008          61          426-441
Structure-activity Relationships of Stemphones, Potentiators of Imipenem Activity against Methicillin-resistant Staphylococcus aureus
Hiroyuki Yamazaki, Nobuhiro Koyama, Satoshi mura and Hiroshi Tomoda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     11-O-methyl-epi-cochlioquinone A
C31H46O8     ÏàËÆ¶È:64.5%
The Journal of Antibiotics          2004          57          59-63
Cochlioquinones and Epi-Cochlioquinones Antagonists of the Human Chemokine Receptor CCR5 from Bipolaris brizae and Stachybotrys chartarum
K. YOGANATHAN,LAY-KIEN YANG,CHRISTINE ROSSANT,YICUN HUANG,SIEWBEE NG,MARK S. BUTLER and ANTONY D. BUSS
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     cochlioquinone A
    ÏàËÆ¶È:63.3%
Bioscience, Biotechnology, and Biochemistry          1994          58          1143-1145
Phytotoxins Produced by the Plant Pathogenic Fungus Bipolaris bicolor El-1
Hisashi Miyagawa, Shinji Nagai, Tetsu Tsurushima, Mamoru Sato, Tamio Ueno, Hiroshi Fukami
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     epi-cochlioquinone A
C30H44O8     ÏàËÆ¶È:63.3%
The Journal of Antibiotics          1996          49          409-413
Epi-cochlioquinone A, a Novel Acyl-CoA: Cholesterol Acyltransferase Inhibitor Produced by Stachybotrys bisbyi
TOMOYUKI FUJIOKA, KEIKO YAO, KIYOSHI HAMANO, TSUYOSHI HOSOYA, TAKESHI KAGASAKI, YOJI FURUKAWA, HIDEYUKI HARUYAMA, SADAO SATO, TEIICHIRO KOGA, YOSHIO TSUJITA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     cochlioquinone A
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          2015          51          270−272
Chemical Constituents of the Fungus Veronaea sp.
Liang Zhou, Xi Zheng, Chun-Ping Wan, Ze-Fen Yu, Ke-Qin Zhang, Guo-Hong Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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