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aydchp: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-09 10:44:19
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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ
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