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535995050: ½ð±Ò+15, ¡ïÓаïÖú 2012-08-08 21:54:15
535995050: ½ð±Ò+5, ¡ï¡ï¡ïºÜÓаïÖú 2012-11-15 16:20:54
1 .     aversin
C20H16O7     ÏàËÆ¶È:80.9%
Magnetic Resonance in Chemistry          2007          45          434-438
1H and 13C NMR assignments for two anthraquinones and two xanthones from the mangrove fungus (ZSUH-36) (pages 434¨C438)
Changlun Shao, Zhigang She, Zhiyong Guo, Hong Peng, Xiaoling Cai, Shining Zhou, Yucheng Gu and Yongcheng Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     8-methoxy-2-(3'-methoxy-4,5-methylenedioxyphenyl)-1-methylquinolin-4-one
     ÏàËÆ¶È:52.3%
Phytochemistry          1996          41          647-649
Alkaloids and coumarins from Esenbeckia species
Fernando M. Oliveira, Antônio Euz¨¦bio G.?Sant'ana, Lucia M. Conserva, Jos¨¦Guilherme S. Maia, Giselle M. P. Guilhon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     gigantol diacetate
    ÏàËÆ¶È:52.3%
Phytochemistry          1993          32          1561-1565
Cumulatin and tristin, two bibenzyl derivatives from the orchids Dendrobium cumulatum and Bulbophyllum triste
P.L. Majumder, S. Pal (n¨¦e Ray)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     6,8-dimethoxy-1-hydroxy-2-hydroxymethyl-3-methyl-9,10-anthraquinone
    ÏàËÆ¶È:52.3%
Tetrahedron Letters          2005          46          2377-2380
An efficient regioselective synthesis of endocrocin and structural related natural anthraquinones starting from emodin
Mario Waser, Bernd Lackner, Joachim Zuschrader, Norbert M¨¹ller, Heinz Falk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     austrocorticinic acid
C19H16O7     ÏàËÆ¶È:52.3%
Journal of the Chemical Society, Perkin Transactions 1          1990                   1159-1167
Pigments of fungi. Part 11. (+)-Austrocorticin, austrocorticinic acid, austrocorticone, and related pigments; the first naturally occurring anthraquinones derived from a propionate-triggered octaketide
Melvyn Gill and Alberto Gim¨¦nez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     5-{[(3,4-dimethoxyphenyl)amino]methyl}-2-fluoroben-zonitrile
    ÏàËÆ¶È:52.3%
Bioorganic & Medicinal Chemistry          2010          18          4056-4066
Synthesis and characterization of potent inhibitors of Trypanosoma cruzi dihydrofolate reductase
Norbert Schormann, Sadanandan E. Velu, Srinivasan Murugesan, Olga Senkovich, Kiera Walker, Bala C. Chenna, Bidhan Shinkre, Amar Desai, Debasish Chattopadhyay
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     1-(2,4-difluoro-phenyl)-5-(3-methoxy-4-prop-2-ynyloxy-phenyl)-penta-1,4-dien-3-one
C21H16F2O3     ÏàËÆ¶È:52.3%
Bioorganic & Medicinal Chemistry          2010          18          8243-8256
Design, synthesis and in vitro antimalarial evaluation of triazole-linked chalcone and dienone hybrid compounds
Eric M. Guantai, Kanyile Ncokazi, Timothy J. Egan, Jiri Gut, Philip J. Rosenthal, Peter J. Smith, Kelly Chibale
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     compound 10
C25H22O8     ÏàËÆ¶È:52.3%
Tetrahedron          1999          55          2529-2544
New oligostilbenes having a benzofuran from Vitis vinifera ¡®Kyohou¡¯
Junko Ito, Yoshiaki Takaya, Yoshiteru Oshima, Masatake Niwa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     rotenone
C23H22O6     ÏàËÆ¶È:52.1%
Journal of Natural Products          1984          Vol 47          692-697
Oxidation of Rotenone by Polyporus anceps Laccase
F. Sima Sariaslani, John M. Beale Jr., John P. Rosazza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     Meso-3,5-diamino-1,2,3,5,6,7-hexahydro-8-(2-methoxy-phenyl)-dicyclopenta-[b,e] pyridine dihydroditrifluoroacetate
C18H22N3O     ÏàËÆ¶È:52.1%
Bioorganic & Medicinal Chemistry          1997          5          1209-1220
Using guanidinium groups for the recognition of RNA and as catalysts for the hydrolysis of RNA
Denise M. Perreault, Larry A. Cabell, Eric V. Anslyn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     rotenone
    ÏàËÆ¶È:52.1%
Journal of the Chemical Society, Perkin Transactions 1          1975                   1497-1499
Carbon-13 magnetic resonance spectra of natural rotenoids and their relatives
Leslie Crombie, Geoffrey W. Kilbee and Donald A. Whiting
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     compound 1a
    ÏàËÆ¶È:52.1%
Journal of the Chemical Society, Perkin Transactions 1          1975                   1497-1499
Carbon-13 magnetic resonance spectra of natural rotenoids and their relatives
Leslie Crombie, Geoffrey W. Kilbee and Donald A. Whiting
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     6'-O-vanillyl esculin
C23H22O12     ÏàËÆ¶È:52.1%
Journal of Integrative Plant Biology          2007          49          218-221
Two New Coumarins from Fraxinus chinensis Rexb.
Dong-Mei Zhang, Li-Li Wang, Jia Li and Li-Hong Hu, *
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     rotenone
    ÏàËÆ¶È:52.1%
Zeitschrift f¨¹r Naturforschung C          2002          57          418-422
New Spirorotenoids from Tephrosia candida
Key words: Tephrosia candida, Fabaceae, Spirorotenoids
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     Compound 5d
C24H24N4O3     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry Letters          2005          15          3133-3136
Synthesis of substituted indole derivatives as a new class of antimalarial agents
Anu Agarwal, Kumkum Srivastava, S.K. Puri, Prem M.S. Chauhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     Compound 5e
C24H24N4O3     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry Letters          2005          15          3133-3136
Synthesis of substituted indole derivatives as a new class of antimalarial agents
Anu Agarwal, Kumkum Srivastava, S.K. Puri, Prem M.S. Chauhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     6,8-di-O-methyl averufin
C22H20O7     ÏàËÆ¶È:50%
Magnetic Resonance in Chemistry          2008          46          886-889
Structural and spectral assignments of six anthraquinone derivatives from the mangrove fungus (ZSUH-36) (pages 886¨C889)
Changlun Shao, Changyun Wang, Meiyan Wei, Shangde Li, Zhigang She, Yucheng Gu and Yongcheng Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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