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[ÇóÖú] ΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë

13CNMR(CDCL3)  20.8,20.9,21.2,40.1,48.7,50.6,51.6,56,64.5,67.8,70.1,76.3,86.2,98.6,100.4,105.2,115.9,117.5,119.6,121,137.4,144.4,147.5,149.7,160.8,163.1,167.4,169.3,169.7,191.5
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Ðìʿѫ: ½ð±Ò+8 2015-05-26 20:30:15
1 .     talaromycesone A
C29H24O11     ÏàËÆ¶È:60%
Marine Biotechnology          2015          17          110−119
Acetylcholinesterase Inhibitors from a Marine Fungus Talaromyces sp. Strain LF458
Bin Wu & Birgit Ohlendorf & Vanessa Oesker & Jutta Wiese & Susann Malien & Rolf Schmaljohann & Johannes F. Imhoff
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     isorhamnetin 3-O-¦Â-D-[4'',6''-di-O-acetylglucopyranosyl(1¡ú3)-¦Â-D-galactopyranoside
    ÏàËÆ¶È:54.8%
Phytochemistry          1992          31          301-303
Four flavonol glycosides from Achlys triphylla
Mizuo Mizuno, Shinji Yoshida, Munekazu Iinuma, Toshiyuki Tanaka, Kazumi Tsuji, Frank A. Lang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     isoscutellarein 7-O-[6'''-O-acetyl-¦Â-D-allopyranosyl-(1¡ú2)-6''-O-acetyl-¦Â-D-glucopyranoside]
    ÏàËÆ¶È:54.8%
Phytochemistry          1987          26          1185-1187
Acetylated allose-containing flavonoid glucosides from Stachys anisochila
Andreas Lenherr,Tom J. Mabry
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     alvaradoin A
C28H30O10     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          98-101
Alvaradoins A-D. Anthracenone C Arabinosides from Alvaradoa jamaicensis
Wayne W. Harding, Geneive E. Henry, Patrick A. Lewis, Helen Jacobs, Stewart McLean, and William F. Reynolds
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     alvaradoin D
C28H30O11     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          98-101
Alvaradoins A-D. Anthracenone C Arabinosides from Alvaradoa jamaicensis
Wayne W. Harding, Geneive E. Henry, Patrick A. Lewis, Helen Jacobs, Stewart McLean, and William F. Reynolds
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     rutin 3''-O-malonate
    ÏàËÆ¶È:53.3%
Journal of Natural Products          1996          59          618-621
A Two-Step Efficient Chemoenzymatic Synthesis of Flavonoid Glycoside Malonates
Sergio Riva, Bruno Danieli and Monica Luisetti
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     bacillosporin A
    ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          1980          28          3649-3655
Isolation and Structures of Oxaphenalenone Dimers from Talaromyces bacillosporus
MIKIO YAMAZAKI and EMI OKUYAMA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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