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1 . hovetrichoside C ÏàËÆ¶È:90.9% Pharmazie 2004 59 297-300 Immunosuppressive auronol glycosides from Artocarpus tonkinensis T. T. Thuy, C. Kamperdick, P. T. Ninh, T. P. Lien, T. T. P. Thao, and T. V. Sung Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . maesopsin 6-O-¦Â-D-glucopyranoside ÏàËÆ¶È:90.9% Chinese Traditional and Herbal Drugs 2014 45 615-621 Chemical constituents from Ficus pumila WEI Wei, FAN Chun-lin, WANG Gui-yang, TANG Hai-jiao, WANG Ying, YE Wen-cai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . hovetrichoside C ÏàËÆ¶È:86.3% Biochemical Systematics and Ecology 2009 37 1-5 Chemical constituents from the fruits of Sonneratia caseolaris and Sonneratia ovata (Sonneratiaceae) Shi-Biao Wu, Ying Wen, Xu-Wen Li, Yun Zhao, Zheng Zhao, Jin-Feng Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 2-hydroxynaringenin-7-O-¦Â-glucoside C21H22O11 ÏàËÆ¶È:86.3% Natural Product Sciences 2000 6 79-81 Flavanone Glycoside from the Fruits of Chaenomeles sinensis Kim, Ho-Kyoung; Jeon, Won-Kyung; Ko, Byoung-Seob Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 2-Hydroxynaringin 5-O-¦Â-D-glucopyranoside C21H22O11 ÏàËÆ¶È:86.3% Journal of Natural Medicines 2009 63 46-51 Chemical constituents of imported Rosae fructus Susumu Kawakami, Katsuyoshi Matsunami, Hideaki Otsuka, Masatoshi Kawahata and Kentaro Yamaguchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . alphitonin 4-O-¦Â-D-glucoside ÏàËÆ¶È:77.2% Pharmazie 2004 59 297-300 Immunosuppressive auronol glycosides from Artocarpus tonkinensis T. T. Thuy, C. Kamperdick, P. T. Ninh, T. P. Lien, T. T. P. Thao, and T. V. Sung Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . maesopsin-6-O-¦Â-D-glucopyranoside ÏàËÆ¶È:77.2% Natural Product Research and Development 2003 15 203-205 FLAVONOIDS AND BIOACTIVITY OF SAGERETIA GRACILIS YANG Ya-bin; TAN Ning-hua; WANG Lin; WANG Shuang-ming;JIA Rui-rui; JIANG Li-hua; FU Xiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . kaempferol 7-methyl ether 4'-¦Â-D-glucopyranoside C22H22O11 ÏàËÆ¶È:63.6% Phytochemistry 1996 42 903-905 Flavonols and isoflavones from Cotoneaster simonsii Elisa Palme, Anna Rita Bilia, Ivano Morelli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Catechin-7-O-¦Â-D-glucopyranoside C21H24O11 ÏàËÆ¶È:63.6% Archives of Pharmacal Research 2011 Vol 34, No 9 1443-1450 Protective Constituents against Sepsis in Mice from the Root Barks of Ulmus davidiana var. japonica Ming Shan Zheng, Gao Li, Ying Li, Chang-Seob Seo, Yeun-Kyung Lee, Jun-Sub Jung, Dong-Keun Song, Hong-Beom Bae, Sang-Hyun Kwak, Hyun-Wook Chang, Jae-Ryong Kim, and Jong-Keun Son Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (+)-catechin-7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:63.6% Chinese Journal of Medicinal Chemistry 2009 19 48-51 Flavanoidal constituents of Choerospondias axillaries and their in vitro antitumor and anti-hypoxia activities LI Chang-wei, CUI Cheng-bin, CAI Bing, HAN Bing, LI Ming-ming, FAN Ming Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 2,4,6-Trihydroxyphenanthrene 2-O-Glucoside ÏàËÆ¶È:63.6% Journal of Agricultural and Food Chemistry 2000 48 2681-2686 Isolation and Characterization of Novel Stilbene Derivatives from Riesling Wine B. Baderschneider and P. Winterhalter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (+)-catechin-7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:63.6% Chinese Traditional and Herbal Drugs 2012 43 1704-1707 Chemical constituents from rhizomes of Bergenia scopulosa (¢ò) CUI Ying Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (2R,3S)-7-(¦Â-D-glucopyranosyloxy)-3,4-dihydro-2-(4-hydroxyphenyl)-2H-1-benzopyran-3,5-diol C21H24O10 ÏàËÆ¶È:59.0% Chemistry & Biodiversity 2007 Vol. 4 32 ANew Flavone Xyloside and Two New Flavan-3-ol Glucosides from Juniperus communis var. depressa Naoki Iida, Yuka Inatomi, Hiroko Murata, Akira Inada, Jin Murata, Frank A. Lang, Nobuyasu Matsuura, and Tsutomu Nakanishi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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