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1 .     eugenyl ¦Â-rutinoside
    ÏàËÆ¶È:86.9%
Chinese Journal of Natural Medicines          2009          7          190-192
Chemical Constituents from the Leaves of Eriobotrya japonica
LI Er-Na; ZHOU Guo-Dong; KONG Ling-Yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Eugenol-O-[¦Â-D-xylopyranosyl-(1f5)-O-¦Â-D-apiofuranosyl-(1¡ú6)-O-¦Â-D-glucopyranoside]
C26H14O38     ÏàËÆ¶È:61.5%
Journal of Agricultural and Food Chemistry          2005          53          2853-2858
Phenylpropanoid Glycosides from Tynanthus panurensis: Characterization and LC-MS Quantitative Analysis
Alberto Plaza, Paola Montoro, Angelyne Benavides, Cosimo Pizza, and Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     2-methoxy-5-(E)-propenyl-phenol-¦Â-vicianoside
C21H30O11     ÏàËÆ¶È:60.8%
Fitoterapia          2006          77          613-614
A new phenolic glycoside from Paeonia lactiflora
Dean Guo , Guan Ye , Hui Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     isorhamnetin 3-O-rhamnoglucoside
C28H24O16     ÏàËÆ¶È:60.7%
Natural Product Sciences          2005          11          233-239
Flavonoids of Gomphocarpus sinaicus and Evaluation of Some Pharmacological Activities
Batran, Seham A. El; Abdel-Azim, Nahla S.; Abdel-Shafeek, Khaled A.; Shahat, Abd-Elatty A.; El-Missiry, Moustafa M.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     peonidin 3-O-(6''-O-¦Á-rhamnopyranosyl-¦Â-glucopyranoside)
    ÏàËÆ¶È:59.2%
Phytochemistry          2003          63          783-787
Anthocyanins from flowers of the orchids Dracula chimaera and D. cordobae
Torgils Fossen, Dag Olav Øvstedal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     rutin
    ÏàËÆ¶È:59.2%
Chinese Journal of Pharmaceuticals          2010          41          98-102
Chemical Constituents of Castanea mollissima Blume Shell
JIA Lu, XI Fang, WANG Na, JING Linlin, KONG Deyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     rutin
C27H30O16     ÏàËÆ¶È:59.2%
Chinese Journal of Pharmaceuticals          2009          40          662-704
Study on Chemical Constituents of Urena lobata L.I.Flavonoid Constituents
JIA Lu, JING Lin-lin, ZHOU Sheng-an, A You-mei, KONG De-yun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     isorhamnetin-3-O-rutinoside
    ÏàËÆ¶È:57.1%
Acta Botanica Yunnanica          2001          23(3)          394-396
Flavonoids from Cinnamomum zeylanicum
MEI Wen-Li, QI Shu-Hua, WU Gao-Fen, CHEN Chang-Xiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     isorhamnetin-3-O-¦Á-L-rhamnopyranosyl-(1¡ú6)-¦Á-D-glucopyranoside
    ÏàËÆ¶È:57.1%
China Journal of Chinese Materia Medica          2012          37          1593-1596
Chemical constituents of Neoalsomitra integrifoliola
SU Dongmin; TANG Wenzhao; YU Shishan; LIU Yunbao; QU Jing; YU Dequan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     6'-O-¦Á-D-galactopyranosylsesamoside
C23H34O17     ÏàËÆ¶È:56.5%
Helvetica Chimica Acta          2007          Vol. 90          143
Iridoid Glycosides from Lamiophlomis rotata
Jun-Jie Tan, Chang-Heng Tan, Mu Li, Shan-Hao Jiang, and Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     4-hydroxy-2- isopropyl-5-methylphenyl O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C22H33H11     ÏàËÆ¶È:56.5%
Helvetica Chimica Acta          2003          Vol. 86          2021
New Glycosides from Salvia moorcroftiana (Lamiaceae)
Muhammad Zahid, Muhammad Saeed, Muhammad Asim, Omar Ishrud, Shihua Wu,Viqar Uddin Ahmad, and Yuanjiang Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     litseaefoloside A
C23H26O12     ÏàËÆ¶È:56.5%
Journal of Natural Products          2005          68          1531-1535
Phenolic and Triterpene Glycosides from the Stems of Ilex litseaefolia
Ai-Lian Zhang, Qi Ye, Bo-Gang Li, Hua-Yi Qi, and Guo-Lin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     6a-HMG-SDG
C38H54O20     ÏàËÆ¶È:56.5%
Journal of Natural Products          2001          64          1388-1397
Biosynthetic Pathway to the Cancer Chemopreventive Secoisolariciresinol Diglucoside-Hydroxymethyl Glutaryl Ester-Linked Lignan Oligomers in Flax (Linum usitatissimum) Seed
Joshua D. Ford, Kai-Sheng Huang, Huai-Bin Wang, Laurence B. Davin, and Norman G. Lewis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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