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rootulysses: ½ð±Ò+25, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£¸Ðл 2013-09-05 22:48:42
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1 .     3,4,5-trimethoxyphenol ¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyronoside
C35H52O20     ÏàËÆ¶È:93.7%
Natural Product Research          2009          23          1408-1415
Phenolic and bis-iridoid glycosides from Strychnos cocculoides
Fortunatus Sunghwa; Mamoru Koketsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2 .     3,4,5-Trimethoxyphenyl 1-O-¦Â-apiofuranosyl (1''¡ú6')-¦Â-glucopyranoside
C20H30O13     ÏàËÆ¶È:88.2%
Phytochemistry          2002          59          551-556
Iridoid and phenolic glycosides from Morinda coreia
Tripetch Kanchanapoom, Ryoji Kasai, Kazuo Yamasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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3 .     3,4,5-trimethoxyphenol ¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:88.2%
Chemical & Pharmaceutical Bulletin          1995          43          1937-1942
Chemical Evaluation of Betula Species in Japan. I.Constituents of Betula ermanii
Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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4 .     2,4,6-trimethoxyphynol-1-O-¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:88.2%
Chinese Traditional and Herbal Drugs          1997          28          195-198
Studies on the Chemical Constituents of Thinleaf Adina(Adina rubella)(¢ó)
Fan Gaojun and He Zhisheng (Address: He Zhisheng; Shanghai Institute of Materia Medica; Chinese Academy of Sciences; Shanghai);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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5 .     3,4,5-trimethoxyphenyl-1-O-¦Â-D-apiofuranosyl-(1''¡ú6')-glucopyranoside
    ÏàËÆ¶È:88.2%
Journal of Chinese Pharmaceutical Sciences          2012          21          88-92
Chemical constituents from Aquilaria sinensis(Lour.) Gilg
Dong Chen; Yue-Lin Song; Chun-Xiao Nie; Xu Ma; Peng-Fei Tu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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6 .     1-Hydroxy-3,4,5-trimethoxybenzene-1-O-¦Á-L-apiopyranosyl-(1¡ú 6)-O-¦Â-D-glucopyranoside
C20H30O13     ÏàËÆ¶È:82.3%
Journal of Asian Natural Products Research          2006          8          571-577
A new meta-homoisoflavane from the fresh stems of dracaena cochinchinensis
Q.-A. ZHENG, Y.-J. ZHANG and C.-R. YANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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7 .     3,4,5-trimethoxyphenol ¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:78.9%
Chemical & Pharmaceutical Bulletin          1997          45          1533-1535
Three New Hemiterpene Glycosides from Ilex macropoda
Hiroyuki FUCHINO,Hironori TACHIBANA and Nobutoshi TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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8 .     3,5-¶þ¼×Ñõ»ù-4-ôÇ»ù±½·Ó1-O-¦Â-D-ÇÛÌÇ»ù-(1¡ú6)-O-¦Â-D-ÆÏÌÑÌÇÜÕ
    ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2008          39          1143-1145
뺼×ÓÉÒ»¯Ñ§³É·ÖµÄÑо¿
ÎÄÆÁ;º«»ÛÓ¢;ÍõÄËÀû;Ò¦ÐÂÉú
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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9 .     3-hydroxy-5-methoxyphenol-2-O-¦Â-apiofuranosyl-(1¡ú2)-¦Â-glucopyranoside
    ÏàËÆ¶È:73.3%
Journal of Natural Products          2001          64          1179-1182
Secondary Metabolites from the Roots of Astragalus zahlbruckneri
Ihsan Çalis,Hasan Abou Gazar, Sonia Piacente, and Cosimo Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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10 .     3,4,5-trimetoxyphenil 1-O-¦Â-(6-sulpho)-glucopyranoside
C15H22O12S     ÏàËÆ¶È:73.3%
Phytochemistry          2009          70          641-649
Phenolic compounds from Bursera simaruba Sarg. bark: Phytochemical investigation and quantitative analysis by tandem mass spectrometry
Mariateresa Maldini, Paola Montoro, Sonia Piacente, Cosimo Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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