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wangwang1989
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
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luky001: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл£¡ 2013-06-21 10:28:54
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luky001: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл£¡ 2013-06-21 10:28:54
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½127¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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