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14.1, 14.2, 21.1, 22.2, 22.3, 22.6, 22.9, 26.0, 26.5, 29.7, 42.2, 45.1, 51.6, 53.0, 55.9, 60.4, 73.9, 82.8, 94.1, 101.3, 105.2, 108.4, 110.3, 116.6, 160.3, 162.2, 168.6, 191.1, 191.9, 200.4, 204.1
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thb237: ½ð±Ò+4, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-25 15:34:39
1 .     englobal-In-2
C28H38O5     ÏàËÆ¶È:54.8%
Natural Medicines          1997          51          486-490
Euglobals-In 2 and -In-3, New Euglobals from Eucalyptus incrassata
TAKASAKI MIDORI,KONOSHIMA TAKAO,KOZUKA MUTSUO,HARUNA MITSUMASA,ITO KAZUO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     dichrostachine H
C36H40O9     ÏàËÆ¶È:52.7%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     dichrostachine L
C36H40O8     ÏàËÆ¶È:51.6%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     4-Acetoxy-plakinamine B
C33H52N2O2     ÏàËÆ¶È:51.5%
Steroids          2007          72          682-685
Acetylcholinesterase-inhibiting steroidal alkaloid from the sponge Corticium sp.
Roosanee Langjae, Somchai Bussarawit, Supreeya Yuenyongsawad, Kornkanok Ingkaninan, Anuchit Plubrukarn
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2
14.1, 14.2, 21.1, 22.2, 22.3, 22.6, 22.9, 26.0, 26.5, 29.7, 42.2, 45.1, 51.6, 53.0, 55.9, 60.4, 73.9, 82.8, 94.1, 101.3, 105.2, 108.4, 110.3, 116.6, 160.3, 162.2, 168.6, 191.1, 191.9, 200.4, 204.1  
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1 .     dichrostachine L
C36H40O8     ÏàËÆ¶È:64.5%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     macrocarpal I
C28H40O6     ÏàËÆ¶È:64.5%
Journal of Natural Products          1996          59          823-827
Macrocarpals H, I, and J from the Leaves of Eucalyptus globulus
Kenji Osawa and Hideyuki Yasuda, Hiroshi Morita, Koichi Takeya, and Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     (5'S)-17¦Â-(1-Acetyl-5-p-fluorophenyl-3-pyrazolinyl)androst-5-en-3¦Â-yl acetate
    ÏàËÆ¶È:64.5%
Steroids          2012          77          566-574
Synthesis of D-ring-substituted (5'R)- and (5'S)-17¦Â-pyrazolinylandrostene epimers and comparison of their potential anticancer activities
Zolt¨¢n Iv¨¢nyi,Nikoletta Szab¨®,Judit Huber,J¨¢nos Wölfling,Istv¨¢n Zupk¨®,Mih¨¢ly Sz¨¦csi,Tibor Wittmann,Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     (5'R)-17¦Â-(1-Acetyl-5-p-cyanophenyl-3-pyrazolinyl)androst-5-en-3¦Â-yl acetate
C33H41N3O3     ÏàËÆ¶È:64.5%
Steroids          2012          77          566-574
Synthesis of D-ring-substituted (5'R)- and (5'S)-17¦Â-pyrazolinylandrostene epimers and comparison of their potential anticancer activities
Zolt¨¢n Iv¨¢nyi,Nikoletta Szab¨®,Judit Huber,J¨¢nos Wölfling,Istv¨¢n Zupk¨®,Mih¨¢ly Sz¨¦csi,Tibor Wittmann,Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     (5'S)-17¦Â-(1-Acetyl-5-p-cyanophenyl-3-pyrazolinyl)androst-5-en-3¦Â-yl acetate
C33H41N3O3     ÏàËÆ¶È:64.5%
Steroids          2012          77          566-574
Synthesis of D-ring-substituted (5'R)- and (5'S)-17¦Â-pyrazolinylandrostene epimers and comparison of their potential anticancer activities
Zolt¨¢n Iv¨¢nyi,Nikoletta Szab¨®,Judit Huber,J¨¢nos Wölfling,Istv¨¢n Zupk¨®,Mih¨¢ly Sz¨¦csi,Tibor Wittmann,Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     dichrostachine B
C36H40O9     ÏàËÆ¶È:63.8%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     elaphogayanin B
C32H44O8     ÏàËÆ¶È:62.5%
Journal of Natural Products          2010          73          901-904
Phloroglucinols from the Argentine Ferns Elaphoglossum gayanum and E. piloselloides
Cecilia Socolsky, Susana A. Borkosky, Marcela Hern¨¢ndez de Ter¨¢n, Yoshinori Asakawa and Alicia Bard¨¢n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     xylocarpin F
C31H38O11     ÏàËÆ¶È:61.2%
Journal of Natural Products          2007          70          772-778
Xylocarpins A-I, Limonoids from the Chinese Mangrove Plant Xylocarpus granatum
Jianxin Cui,Jun Wu,Zhiwei Deng, Peter Proksch,and Wenhan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     macrocarpal J
C28H40O6     ÏàËÆ¶È:61.2%
Journal of Natural Products          1996          59          823-827
Macrocarpals H, I, and J from the Leaves of Eucalyptus globulus
Kenji Osawa and Hideyuki Yasuda, Hiroshi Morita, Koichi Takeya, and Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     compound 4
    ÏàËÆ¶È:61.2%
Chemistry of Natural Compounds          2001          37          343-346
13C NMR SPECTRA OF 5- AND 7-BROMO-6-KETOSTEROIDS AND RELATED COMPOUNDS
N. V. Kovganko, S. N. Sokolov, and V. L. Survilo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     elaphogayanin A
C30H40O8     ÏàËÆ¶È:61.2%
Journal of Natural Products          2010          73          901-904
Phloroglucinols from the Argentine Ferns Elaphoglossum gayanum and E. piloselloides
Cecilia Socolsky, Susana A. Borkosky, Marcela Hern¨¢ndez de Ter¨¢n, Yoshinori Asakawa and Alicia Bard¨¢n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     7¦Â-acetoxi-20R-hidroxi-5¦Â,6¦Â-epoxi-1,4-dioxo-vita-2,24-dienolido
    ÏàËÆ¶È:61.2%
Qu¨ªmica Nova          2011          34          237-241
Cytotoxic derivatives of withanolides isolated from the leaves of Acnistus arborescens
Minguzzi, Sandro; Barata, Lauro E. S.; Cordell, Geoffrey A.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     (3¦Á,5¦Á,6¦Â,22R,4'S,5'S)-22-Acetoxy-3,5-cyclo-6-methoxy-22-(3'-methyl-4'-methoxycarbonyl-isoxazolin-5'-yl)-23,24-dinorcholane
C31H47O6N     ÏàËÆ¶È:61.2%
Steroids          2013          78          823-831
Regio- and stereocontrolled synthesis of novel steroidal isoxazolines: A new route to the formation of selectively modified steroid side chains
Halina Zhylitskaya, Raisa Litvinovskaya, Alexander Baranovsky, V¨¢clav Eigner, Bohumil Kratochv¨ªl, Pavel Drašar, Vladimir Khripach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     (5'R)-17¦Â-(1'-acetyl-5'-phenyl-1H-pyrazolin-3'-yl)-5¦Á-androstan-3¦Â-yl acetate
C32H44N2O3     ÏàËÆ¶È:61.2%
Steroids          2014          87          86-92
Synthesis of steroidal derivatives containing substituted, fused and spiro pyrazolines
Anabel Romero-L¨®pez, Sara Montiel-Smith, Socorro Meza-Reyes, Pen¨¦lope Merino-Montiel, Jos¨¦ Luis Vega-Baez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     rhodomyrtal B
C28H40O6     ÏàËÆ¶È:61.2%
RSC Advances          2014          4          13514-13517
Rhodomyrtals A¨CD, four unusual phloroglucinolsesquiterpene adducts from Rhodomyrtus psidioides
Qingyao Shou, Joshua E. Smith, Htwe Mon, Zlatko Brkljača, Ana-Sunčana Smith, David M. Smith, Hans J. Griesser and Hans Wohlmuth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     dichrostachine C
C36H40O8     ÏàËÆ¶È:61.1%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     dichrostachine E
C36H40O10     ÏàËÆ¶È:61.1%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     dichrostachine F
C36H44O9     ÏàËÆ¶È:61.1%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     dichrostachine H
C36H40O9     ÏàËÆ¶È:61.1%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------


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