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ÃÀÀöµÄС¹ÃÄï: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-21 14:48:02
1 .     compound 5
    ÏàËÆ¶È:62.5%
Bioscience, Biotechnology, and Biochemistry          1995          59          316-318
New Lactarane Sesquiterpenoid from the Fungus Russula emetica
Kenji Kobata, Satoshi Kano, Hisao Shibata
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     9¦Â-hydroxy-2¦Â-methoxyclovan-10-one
C16H26O3     ÏàËÆ¶È:56.2%
Journal of Natural Products          2004          67          793-798
Structure−Activity Relationships in the Fungistatic Activity against Botrytis cinerea of Clovanes Modified on Ring C
Athina Deligeorgopoulou, Antonio J. Macas-Snchez, Daniel J.Mobbs, Peter B. Hitchcock, James R. Hanson, and Isidro G. Collado
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     suberosanone
C15H24O     ÏàËÆ¶È:56.2%
Journal of Natural Products          2000          63          1603-1607
New Cytotoxic Sesquiterpenes from the Gorgonian Isis hippuris
Jyh-Horng Sheu,Kuang-Chih Hung, Guey-Horng Wang, and Chang-Yih Duh
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     1¦Â,5¦Á,9,9-tetramethyltricyclo[6.2.1.0(4.11)]undec-5-ene
    ÏàËÆ¶È:56.2%
Journal of Natural Products          1994          Vol 57          738
Inhibition of Botrytis cinerea by New Sesquiterpenoid Compounds Obtained from the Rearrangement of Isocaryophyllene
Isidro G. Collado, Josefina Aleu, Antonio J. Mac¨ªas-S¨¢nchez, Rosario Hern¨¢ndez-Gal¨¢n
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     (+)-12-hydroxycedrol
C15H26O2     ÏàËÆ¶È:56.2%
Phytochemistry          1995          40          69-72
The in vitro biosynthesis of indole-3-butyric acid in maize
Jutta Ludwig-M¨¹ller, Willy Hilgenberg, Ephraim Epstein
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     cedran-8¦Â,12-diol
C15H26O2     ÏàËÆ¶È:56.2%
Phytochemistry          1993          33          835-837
Biotransformation of the sesquiterpenoid, cedrol, by Cephalosporium aphidicola
James R. Hanson, Habib Nasir
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     8¦Â-Hydroxyginsenol
C15H26O2     ÏàËÆ¶È:56.2%
Journal of the Chemical Society, Perkin Transactions 1          1999                   727-730
Biotransformation of the fungistatic sesquiterpenoid ginsenol by Botrytis cinerea
Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, James R. Hanson, Peter B. Hitchcock and Isidro G. Collado
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     ¦Á-cedr ol
    ÏàËÆ¶È:56.2%
Natural Product Research and Development          2002          14(2)          1-6
THE CHEMICAL CONSTITUENTS OF COLEUS FORSKOHLII
YAO Chun-suo SHEN Yun-heng XU Yun-long
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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