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sdw1291112

½ð³æ (СÓÐÃûÆø)

[ÇóÖú] ΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë

13C NMR (126 MHz, cd3od)
9.20,10.11,10.53,17.79,18.57,22.13,36.41,36.96,39.86,60.19,62.93,75.70,106.68,111.59,112.22,112.50,115.57,118.50,132.79,145.24,149.48,149.72,153.97,161.68,172.81
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sdw1291112: ½ð±Ò+10, ¡ïÓаïÖú 2015-05-23 14:21:07
1 .     formoxanthone C
C23H24O6     ÏàËÆ¶È:52.1%
Phytochemistry          2006          67          723-727
Antibacterial and cytotoxic xanthones from the roots of Cratoxylum formosum
Sompong Boonsri, Chatchanok Karalai, Chanita Ponglimanont,Akkharawit Kanjana-opas, Kan Chantrapromma
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     (1R*,3R*,5S*,6R*,7S*,9Z)-8-methyl-5-(2'-acetoxy-1',5'-dimethylhex-4'-enyl)-z-methylenebicyclo95.3.0]dec-9-ene-3,6,8-triol
C22H34O5     ÏàËÆ¶È:52.1%
Planta Medica          1993          59          174-178
Four New Hydroazulenoid Diterpenes from the Tropical Marine Brown Alga Dictyota volubilis
Gabriele M. Kdnig,AnthonyB. Wright , Otto Sticher,and Heinz R¨¹egger
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     Schininallylol
    ÏàËÆ¶È:52.1%
Phytochemistry          1995          39          1091-1097
Coumarins and anti-platelet aggregation constituents from Zanthoxylum schinifolium
Ih-Sheng Chen, Yuh-Chwen Lin, Ian-Lih Tsai, Che-Ming Teng, Feng-Nien Ko, Tsutomu Ishikawa, Hisashi Ishii
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     14-hydroxycolladonin
C24H30O5     ÏàËÆ¶È:50%
Phytochemistry          1992          31          3211-3213
Coumarins from Heptaptera anisoptera
Giovanni Appendino, Hasan Çetin Özen, Silvia Tagliapietra, Marco Cisero
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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2Â¥2015-05-22 17:06:43
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