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²éѯ½á¹û£º¹²²éµ½180¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (2R,3R)-8-(3,3-dimethylallyl)-2,3-dihydro-4',5,7-trihydroxyflavonol 7-[O-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside] C32H40O16 ÏàËÆ¶È:62.8% Helvetica Chimica Acta 2007 Vol. 90 2186 8-(3,3-Dimethylallyl)-Substituted Flavonoid Glycosides from the Aerial Parts of Epimedium koreanum Hai-Yu Zhao, Li Fan, Lei Zhou, Jian Han, Bao-Rong Wang, and De-An Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . apigenin 8-C-(2''-O-(E)-p-coumaroyl-¦Â-glucopyranoside) ÏàËÆ¶È:62.8% Journal of Agricultural and Food Chemistry 2010 58 7211-7217 Flavone C-Glycosides from Seeds of Fenugreek, Trigonella foenum-graecum L. Saleh Rayyan, Torgils Fossen and Øyvind M. Andersen Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . quercetin 5,7,4'-tri-O-¦Â-D-glucopyranoside C33H40O22 ÏàËÆ¶È:60% Phytochemistry 2002 59 275-278 Flavonoid 5-glucosides from the cocoon shell of the silkworm, Bombyx mori Yasumori Tamura, Ken-ichi Nakajima, Ken-ichi Nagayasu, Chiyuki Takabayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . aescuflavoside C38H48O25 ÏàËÆ¶È:60% Journal of Natural Products 2004 67 650-653 Antiviral Flavonoids from the Seeds of Aesculus chinensis Feng Wei, Shuang-Cheng Ma, Lin-Yun Ma, Paul Pui-Hay But, Rui-Chao Lin, and Ikhlas A. Khan Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . kaempferol-3-O-(O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-[¦Â-D-glucopyranosyl-(1¡ú3)]-¦Â-D-galactopyranoside) C33H40O20 ÏàËÆ¶È:60% Planta Medica 2012 78 703-710 Passos Oliveira, Adriana; Raith, Melanie; Kuster, Ricardo Machado; Rocha, Leandro Machado; Hamburger, Matthias; Potterat, Olivier: Metabolite Profiling of the Leaves of the Brazilian Folk Medicine Sideroxylon obtusifolium Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 4 C36H44O20 ÏàËÆ¶È:58.3% Acta Pharmaceutica Sinica 1997 32 451-454 STUDIES ON THE FLAVONOIDS FROM DENDRANTHEMA LAVANDULIFOLIUM YX Shen; LH Quan; L Guan and JM Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ent-epiafzelechin-(2¦Á¡úO¡ú7,4¦Á¡ú8)-ent-afzelechin 3'-O-¦Â-D-glycopyranoside C36H34O15 ÏàËÆ¶È:58.3% Journal of Natural Products 2013 76 1881-1888 Proanthocyanidins from Spenceria ramalana and Their Effects on AGE Formation in Vitro and Hyaloid-Retinal Vessel Dilation in Larval Zebrafish in Vivo Ik-Soo Lee, Song Yi Yu, Seung-Hyun Jung, Yu-Ri Lee, Yun Mi Lee, Joo-Hwan Kim, Hang Sun, and Jin Sook Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . isovitexin 2''-O-(6'''-(E)-p-coumaroyl)glucoside-4'-O-glucoside C42H46O22 ÏàËÆ¶È:57.8% Phytochemistry 2001 58 167-172 Acylated flavone C-glycosides from Cucumis sativus Mamdouh M. Abou-Zaid, Domenic A. Lombardo, Geoffrey C. Kite,Ren¨¦e J. Grayerb, Nigel C. Veitch Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . acacetin-7-O-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl-(1¡ú2)-[¦Á-L-rhamnopyranosyl-(1¡ú6)]-¦Â-D-glucopyranoside C40H52O24 ÏàËÆ¶È:57.5% Journal of Natural Products 2013 76 186-193 Flavone Tetraglycosides and Benzyl Alcohol Glycosides from the Mongolian Medicinal Plant Dracocephalum ruyschiana Erdenechimeg Selenge, Toshihiro Murata, Kyoko Kobayashi, Javzan Batkhuu, and Fumihiko Yoshizaki Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . aescuflavoside A C33H40O21 ÏàËÆ¶È:57.1% Journal of Natural Products 2004 67 650-653 Antiviral Flavonoids from the Seeds of Aesculus chinensis Feng Wei, Shuang-Cheng Ma, Lin-Yun Ma, Paul Pui-Hay But, Rui-Chao Lin, and Ikhlas A. Khan Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 6'''-hydroxylophirone B 4'''-O-¦Â-glucoside C36H33O14 ÏàËÆ¶È:57.1% Journal of Natural Products 2002 65 1027-1029 Novel Biflavonoids from the Stem Bark of Ochna integerrima Rawiwun Kaewamatawong,Kittisak Likhitwitayawuid, Nijsiri Ruangrungsi, Hiromitsu Takayama,Mariko Kitajima, and Norio Aimi Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . acacetin 7-O-(2'''-O-rhamnosyl-2''-O-glucosyl)glucoside ÏàËÆ¶È:57.1% Phytochemistry 1997 44 533-536 Four flavonoid glycosides from Peganum harmala Mohamed Sharaf, Mohamed A. El-Ansari, Stephen A. Matlin, Nabiel A. M. Saleh Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 2'''-O-rhamnosyl-2''-O-glucosylcytisoside ÏàËÆ¶È:57.1% Phytochemistry 1997 44 533-536 Four flavonoid glycosides from Peganum harmala Mohamed Sharaf, Mohamed A. El-Ansari, Stephen A. Matlin, Nabiel A. M. Saleh Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2''-p-Coumaroyluitexin 7-glucoside ÏàËÆ¶È:57.1% Phytochemistry 1984 23 2106-2108 2¡å-p-coumaroylvitexin 7-glucoside from Mollugo oppositifolia J. Chopin, G. Dellamonica, K.R. Markham, A.G.Ramachandran Nair, R. Gunasegaran Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3',4',5',6-tetramethoxy 7-O-¦Â-D-glucopyranosyl (1¡ú3) ¦Â-D-glucopyranoside C31H38O17 ÏàËÆ¶È:57.1% Journal of Ethnopharmacology 2011 135 78-87 Chemical constituents from the stem bark of Symplocos paniculata Thunb. with antimicrobial, analgesic and anti-inflammatory activities Ruchi Badoni Semwal, Deepak Kumar Semwal, Ravindra Semwal, Randhir Singh, Mohan Singh Maniyari Rawat Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . quercetin 3-O-{2''-(6'''-p-cumarol-¦Â-D-glucopyranosyl)-¦Á-L-arabinopyranosyl}-7''-O-¦Â-D-glucopyranoside C41H44O22 ÏàËÆ¶È:56.7% Natural Medicines 2000 54 101-103 Two New Flavonol Glycosides from Morettia philaena Growing in Egypt SINGAB ABDEL-NASER B.,KOUGUCHI SHIGERU,SHIBANO MAKIO,KUSANO GENJIRO Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 2'',2'''-di-O-glucosyl vicenin II ÏàËÆ¶È:56.4% Phytochemistry 1997 45 1529-1532 Flavonoids from Ephedra aphylla Sahar A. M. Hussein, Heba H. Barakat, Mahmoud A. M. Nawar, G¨¹nter Willuhn Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . theaflavanoside IV C38H50O23 ÏàËÆ¶È:55.5% Heterocycles 2007 71 1193-1201 New Flavanone Oligoglycosides, Theaflavanosides I, II, III, and IV, with Hepatoprotective Activity from the Seeds of Tea Plant (Camellia sinensis) Ning Li, Toshio Morikawa, Hisashi Matsuda, Kiyofumi Ninomiya, Xian Li, and Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (+)-Tingitanol A C40H42O16 ÏàËÆ¶È:55% Phytochemistry Letters 2009 2 148-151 Stilbene glucosides from the bulbs of Iris tingitana Salwa F. Farag, Yoshiaki Takaya, Masatake Niwa Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 8-(3,3-dimethylallyl)-4',5,7-trihydroxyflavonol 7-[O-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside] C32H38O16 ÏàËÆ¶È:54.2% Helvetica Chimica Acta 2007 Vol. 90 2186 8-(3,3-Dimethylallyl)-Substituted Flavonoid Glycosides from the Aerial Parts of Epimedium koreanum Hai-Yu Zhao, Li Fan, Lei Zhou, Jian Han, Bao-Rong Wang, and De-An Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . gnemonol E C40H42O16 ÏàËÆ¶È:54.2% |
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