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1 .     compound 1
C24H31NO7     ÏàËÆ¶È:96%
The Journal of Antibiotics          1996          49          693-696
A Cholesteryl Ester Transfer Protein Inhibitor from an Insect-associated Fungus
JULIE C. LEE, STEPHEN J. COVAL, JON CLARD
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     apiosporamide
C24H31NO6     ÏàËÆ¶È:80%
Journal of Natural Products          1994          Vol 57          1696
Apiosporamide, a New Antifungal Agent from the Coprophilous Fungus Apiospora montagnei
Ali A. Alfatafta, James B. Gloer, James A. Scott, David Malloch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     12-epi-15-acetylnapelline
C24H35NO4     ÏàËÆ¶È:60%
Planta Medica          2005          71          1073-1076
Three New Diterpene Alkaloids from the Roots of Aconitum nagarum var.lasiandrum
Fan Zhang , Shu-Lin Peng , Xun Liao , Kai-Bai Yu , Li-Sheng Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (5'R)-17¦Â-[2-phenyl)-4,5-dihydrooxazol-5-yl]androst-5-en-3¦Â-ol
C29H41NO2     ÏàËÆ¶È:57.6%
Steroids          2009          74          1025-1032
Steroselective synthesis of some steroidal oxazolines, as novel potential inhibitors of 17¦Á-hydroxylase-C17,20-lyase
D¨®ra Ondr¨¦, J¨¢nos Wölfling, Istv¨¢n T¨®th, Mih¨¢ly Sz¨¦csi, J¨¢nos Julesz, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (5'R)-17¦Â-[2-(4-fluorophenyl)-4,5-dihydrooxazol-5-yl]androst-5-en-3¦Â-ol
C28H36FNO2     ÏàËÆ¶È:57.6%
Steroids          2009          74          1025-1032
Steroselective synthesis of some steroidal oxazolines, as novel potential inhibitors of 17¦Á-hydroxylase-C17,20-lyase
D¨®ra Ondr¨¦, J¨¢nos Wölfling, Istv¨¢n T¨®th, Mih¨¢ly Sz¨¦csi, J¨¢nos Julesz, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (5'R)-17¦Â-[2-(2-chlorophenyl)-4,5-dihydrooxazol-5-yl]androst-5-en-3¦Â-ol
C28H36ClNO2     ÏàËÆ¶È:57.1%
Steroids          2009          74          1025-1032
Steroselective synthesis of some steroidal oxazolines, as novel potential inhibitors of 17¦Á-hydroxylase-C17,20-lyase
D¨®ra Ondr¨¦, J¨¢nos Wölfling, Istv¨¢n T¨®th, Mih¨¢ly Sz¨¦csi, J¨¢nos Julesz, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (rel 5S,6R,8R,9R,10S,13S,15S,16S)-6-acetoxy-9,13;15,-16-diepoxy-15,16-dimethoxylabdane
    ÏàËÆ¶È:56%
Journal of Natural Products          1999          62          1532-1537
Diterpenes from the Fruits of Vitex rotundifolia
Masateru Ono, Megumi Yamamoto, Chikako Masuoka, Yasuyuki Ito, Masami Yamashita, and Toshihiro Nohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     finetianine
C21H29NO3     ÏàËÆ¶È:56%
Planta Medica          2005          71          1073-1076
Three New Diterpene Alkaloids from the Roots of Aconitum nagarum var.lasiandrum
Fan Zhang , Shu-Lin Peng , Xun Liao , Kai-Bai Yu , Li-Sheng Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     7,12-diketolithocholic acid
    ÏàËÆ¶È:56%
Steroids          2006          71          469-475
Regio- and stereoselective reductions of dehydrocholic acid
Giancarlo Cravotto, Arianna Binello, Luisa Boffa, Ornelio Rosati, Marco Boccalini, Stefano Chimichi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     apiosporamide
C24H31NO6     ÏàËÆ¶È:56%
Journal of Natural Products          1994          Vol 57          1696
Apiosporamide, a New Antifungal Agent from the Coprophilous Fungus Apiospora montagnei
Ali A. Alfatafta, James B. Gloer, James A. Scott, David Malloch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 5e
C25H32O3     ÏàËÆ¶È:56%
Chemical Journal of Chinese Universities          2006          27          2101-2105
Synthesis and Anti-tumor Activities of a Series of Novel Tricycle Diterpenes
XIONG Yi,WANG Kui-Wu,PAN Yuan-Jiang, SUN Hong-Xiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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