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184.6, 167.4, 164.9, 163.6, 159.5, 151.8, 147.7, 124.1, 121.2, 117.5, 114.9, 107.6, 104.9, 103.4, 101.5, 100.8, 96.6, 77.7, 75.4, 74.8, 72.9, 72.8, 70.8, 70.6, 67.9, 19.1
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yjl2007

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19.1,69.7,70.6,70.8,72.8,72.9,74.8,75.4,77.7,96.6,100.8,101.5,103.4,104.9,107.6,114.9,117.5,121.2,124.1,147.7,151.8,159.5,163.6,164.9,167.4,184.6
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3Â¥2014-01-21 14:42:02
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yjl2007

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19.1,69.7,70.6,70.8,72.8,72.9,74.8,75.4,77.7,96.6,100.8,101.5,103.4,104.9,107.6,114.9,117.5,121.2,124.1,147.7,151.8,159.5,163.6,164.9,167.4,184.6
4Â¥2014-01-21 14:42:45
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2Â¥: Originally posted by ׿Խ_ÏÈ·æ at 2014-01-21 14:26:49
°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺
È磺21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

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5Â¥2014-01-21 14:59:47
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yjl2007: ½ð±Ò+10 2014-01-21 15:24:22
²éѯ½á¹û£º¹²²éµ½579¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     luteolin-7-O-¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:88.8%
Natural product sciences          2011          17          261-266
Superoxide Quenching Activity of Phenolic Compounds from the Whole Plant of Galium verum var. asiaticum
Kim, Dae-Keun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     luteolin 7-O-¦Á-L-rhamnosyl(1¡ú6)-¦Â-D-glucoside
    ÏàËÆ¶È:85.1%
Phytochemistry          1999          50          293-296
A taraxasterol derivative and phenolic compounds from Hieracium gymnocephalum
S.D. Petrovi, M.S. Gorunovic, V. Wray, I. Merfort
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     kurilensin A
C26H28O14     ÏàËÆ¶È:80.7%
Phytochemistry          2008          69          1419-1424
Antioxidant C-glycosyl flavones from the leaves of Sasa kurilensis var. gigantea
Tatsuya Hasegawa, Ayumi Tanaka, Akiko Hosoda, Fumihide Takano, Tomihisa Ohta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Luteolin 7-O-(6"-O-¦Â-D-apiofuranosyl)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:80.7%
Phytochemistry          1998          48          573-575
Flavonoids from Phlomis nissolii
Franz Bucar, Stefan Ninov, Iliana Ionkova, Theodor Kartnig, Manfred Schubert-Zsilavecz, Ivan Asenov, Belma Konuklugil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     6-C-[2'-O-¦Á-L-Rhamnopyranosyl-(1''¡ú2')]-¦Á-L-arabinopyranosylluteolin
C26H28O14     ÏàËÆ¶È:80.7%
Journal of Natural Products          2010          73          1973-1978
Spectroscopic Characterization and Antiproliferative Activity on HepG2 Human Hepatoblastoma Cells of Flavonoid C-Glycosides from Petrorhagia velutina
Severina Pacifico, Monica Scognamiglio, Brigida D,Abrosca, Simona Piccolella, Nikolaos Tsafantakis, Marialuisa Gallicchio, Andreina Ricci, and Antonio Fiorentino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     apigenin-7-O-¦Â-D-neohesperidoside
    ÏàËÆ¶È:76.9%
Chinese Pharmaceutical Journal          2012          47          261-264
Study on the Chemical Constituents of Terpinia arguta
LI Yun-qiu; LEI Xin-xin; FENG Yu-lin; XU Qiong-ming; XU Li-zhen; YANG Shi-lin;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Chrysoeriol 7-O-[¦Á-L-rhamnopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside]
C28H32O15     ÏàËÆ¶È:75%
Journal of Agricultural and Food Chemistry          2011          59          9581-9587
Isolation and Identification of Flavonoids Accumulated in Proanthocyanidin-free Barley
Hiroshi Nakano, Naoyuki Kawada, Mitsuru Yoshida, Hiroshi Ono, Rika Iwaura, and Takuji Tonooka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     6-C-[2-O-¦Á-L-Rhamnopyranosyl-(1''¡ú2')]-¦Â-D-xylopyranosylluteolin
C26H28O14     ÏàËÆ¶È:73.0%
Journal of Natural Products          2010          73          1973-1978
Spectroscopic Characterization and Antiproliferative Activity on HepG2 Human Hepatoblastoma Cells of Flavonoid C-Glycosides from Petrorhagia velutina
Severina Pacifico, Monica Scognamiglio, Brigida D,Abrosca, Simona Piccolella, Nikolaos Tsafantakis, Marialuisa Gallicchio, Andreina Ricci, and Antonio Fiorentino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     caffeic acid
    ÏàËÆ¶È:73.0%
Korean Journal of Pharmacognosy          2012          43          213-216
Phenolic Components from the Aerial Parts of Bromus japonicus Thunb.
Tao, Chao; Ahn, Dal-Rae; Xing, Ming Ming; Lee, Eun-Byeol; Kim, Dae-Keun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     luteolin-7-O-¦Â-D-glucuronide
C21H18O12     ÏàËÆ¶È:73.0%
The Chinese Pharmaceutical Journal          2003          55          65-70
Chemical Constituents of Verbena bonariensis
Chien-Chih Chen*, Hui-Ying Huang, Chien-Chang Shen, Yu-Lin Huang and Jun-Chih Ou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     luteolin-7-O-glucuronide
C21H18O12     ÏàËÆ¶È:73.0%
Journal of Ethnopharmacology          2013          145          11-17
Antinociceptive, anti-inflammatory and antioxidant activities of aqueous extract from Remirea maritima (Cyperaceae)
A.S. Rabelo, I.D. Oliveira, A.G. Guimarães, J.S.S Quintans, A.P.N. Prata, D.P. Gelain, E.M. Venceslau, J.P.A. Santos, L.J. Quintans-J¨²nior, L.R. Bonjardim, A. Barison, F.R. Campos, A.D.C. Santos, P.C.L. Nogueira, E.V. Costa, V.R.S. Moraes, A.A.S. Ara¨²jo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     luteolin 7-O-¦Â-D-glucuronopyranoside
C21H18O12     ÏàËÆ¶È:73.0%
Journal of Agricultural and Food Chemistry          2001          49          753-758
Alfalfa (Medicago sativa L.) Flavonoids. 1. Apigenin and Luteolin Glycosides from Aerial Parts
Anna Stochmal, Sonia Piacente, Cosimo Pizza, Francesco De Riccardis, Rick Leitz, and Wieslaw Oleszek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ax-4''-OH-maysin
    ÏàËÆ¶È:73.0%
Journal of Agricultural and Food Chemistry          1995          43          2740-2745
New C-4''-Hydroxy Derivatives of Maysin and 3'-Methoxymaysin Isolated from Corn Silks (Zea mays)
Maurice E. Snook, Neil W. Widstrom, Billy R. Wiseman, Patrick F. Byrne, John S. Harwood, Catherine E. Costello
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     luteolin 7-O-(6''-p-nemzoylglucoside
C28H34O13     ÏàËÆ¶È:71.4%
Phytochemistry          1997          46          521-524
Cytotoxic flavonoids from Vitex agnus-castus
Chieko Hirobe, Zhi-Sheng Qiao, Koichi Takeya, Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     5,7,3',4'-tetrahydroxy-8-C-[¦Â-D-apiose-(1¡ú4)]-¦Â-D-glycopyranosyl flavone
C26H28O15     ÏàËÆ¶È:69.2%
Chinese Chemical Letters          2007          18          1231-1234
Two new C-glycosylflavones from Mimosa pudica
Ke Yuan, Jie Li Lu, An Jia, Jian Xin Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Apigenin-7-rutinoside
    ÏàËÆ¶È:69.2%
Journal of Chinese Pharmaceutical Sciences          1996          5          105-108
PhenylpropanoidGlycosidesandFlavonoidGlycosidesIsolatedfromBudsofBuddlejaoficinalisMaxim
Hu-YiZhang and Jing-Xian Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     6-trans-(2'-O-¦Á-rhamnopyranosyl)ethenyl-5,7,3',4'-tetrahydroxyflavone
C23H22O11     ÏàËÆ¶È:69.2%
Journal of Ethnopharmacology          2008          118          71-78
Flavonoids with iNOS inhibitory activity from Pogonatherum crinitum
Guei-Jane Wang, Yi-Min Chen, Teng-Mao Wang, Ching-Kuo Lee, Ke-Jun Chen, Tzong-Huei Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     luteolin 7-O-glucoside
    ÏàËÆ¶È:69.2%
Natural Medicines          1995          49          340-342
Studies on Constituents of Plantaginis Herba 7 : Flavonoids from Plantago asiatica and P. hostifolia
NISHIBE SANSEI,MURAI MICHIKO,TAMAYAMA YASUHIKO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     apigenin-7-O-¦Â-neohesperidoside
C27H30O14     ÏàËÆ¶È:69.2%
Acta Pharmaceutica Sinica B          2011          1          36-39
A new norlignan lignanoside from Selaginella moellendorffii Hieron
Wei-sheng Feng, Ke-ke Li, Xiao-ke Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     chrysoeriol 6-C-¦Â-boivinopyranosyl-7-O-¦Â-glucopyranoside
C28H32O14     ÏàËÆ¶È:67.8%
Journal of Natural Products          2003          66          564-565
Two Flavone C-Glycosides from the Style of Zea mays with Glycation Inhibitory Activity
Ryuichiro Suzuki, Yoshihito Okada, and Toru Okuyama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     Narcissin
    ÏàËÆ¶È:67.8%
Archives of Pharmacal Research          2003          26          1018-1023
Constituents of the stems and fruits of Opuntia ficus-indica var. saboten
Eun Ha Lee, Hyoung Ja Kim, Yun Seon Song, Changbae Jin and Kyung-Tae Lee, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     apigenin-7-O-¦Â-D-(2'',6''-di-¦Á-rhamnopyran-osyl)-glucopyranoside
    ÏàËÆ¶È:67.7%
Chinese Pharmaceutical Journal          2012          47          261-264
Study on the Chemical Constituents of Terpinia arguta
LI Yun-qiu; LEI Xin-xin; FENG Yu-lin; XU Qiong-ming; XU Li-zhen; YANG Shi-lin;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     5,7,3',4'-tetrahydroxy-6-C-[¦Á-L-rhamnopyranosyl-(1¡ú2)]-¦Â-D-glucopyranosyl flavone
C27H30O15     ÏàËÆ¶È:66.6%
Acta Pharmaceutica Sinica          2006          Vol 41          435-438
Chemical constituents of C-glycosylflavones from Mimosa pudica
YUAN Ke; L Jie-li; YIN Ming-wen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     luteolin-8-C-¦Á-L-rhamnopyranosyl(1¡ú2)quinovopyranoside
C27H30O14     ÏàËÆ¶È:66.6%
Zeitschrift f¨¹r Naturforschung C          2002          57          983-985
Flavonoids and Arbutin from Turnera diffusa
S. Piacente, E. E. S. Camargo, A. Zampelli, J. S. Gracioso, A. R. S. Brito, C. Pizza, and W. Vilegas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     Rhoifolin
    ÏàËÆ¶È:66.6%
Food Chemistry          2010          120          134-139
Phenolic constituents from the flower buds of Lonicera japonica and their 5-lipoxygenase inhibitory activities
Eun Ju Lee, Ju Sun Kim, Hyun Pyo Kim, Je-Hyun Lee, Sam Sik Kang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     5,7,3',4'-tetrahydroxy-6-C-[¦Á-L-rhamnopyranosyl-(1¡ú2)]-¦Â-D-glucopyranosylflavone
C27H30O15     ÏàËÆ¶È:66.6%
Chinese Journal of Pharmaceuticals          2012          43          263-267
Isolation and Structural Identification of C-Glycosylflavones from Callicarpa kwangtungensis Chun.and Their Preliminary Anti-inflammatory Activities
JIA An, YANG Yifang, KONG Deyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     apigenin-7-O-neohespiridoside
    ÏàËÆ¶È:66.6%
Pharmaceutical Chemistry Journal          2012          46          35-44
Isolation and structure elucidation of natural antioxidants from leaves of Rauvolfia beddomethe ¨Can endemic/endangered medicinal plant from SouthWestern Ghats of India
V. Divya Nair, R. Gopi, R. Panneerselvam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     apigenin 7-O-[¦Â-D-glucuronopyranosyl(¡ú2)-O-¦Â-D-glucuronopyranoside]
C27H26O17     ÏàËÆ¶È:66.6%
Journal of Agricultural and Food Chemistry          2001          49          753-758
Alfalfa (Medicago sativa L.) Flavonoids. 1. Apigenin and Luteolin Glycosides from Aerial Parts
Anna Stochmal, Sonia Piacente, Cosimo Pizza, Francesco De Riccardis, Rick Leitz, and Wieslaw Oleszek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     Quercetin-3-O-¦Á-L-rhamnopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:66.6%
Journal of Agricultural and Food Chemistry          2001          49          4478-4481
Flavonol Glycosides and Novel Iridoid Glycoside from the Leaves of Morinda citrifolia
Shengmin Sang, Xiaofang Cheng, Nanqun Zhu, Ruth E. Stark, Vladimir Badmaev, Geetha Ghai, Robert T. Rosen, and Chi-Tang Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     apigenin 7-O-¦Á-L-3-O-acetylrhamnopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside
C29H32O15     ÏàËÆ¶È:65.5%
Journal of Natural Products          2004          67          725-727
Acetylated Flavonoid Glycosides Potentiating NGF Action from Scoparia dulcis
Yushan Li, Xigui Chen, Masayuki Satake, Yasukatsu Oshima, and Yasushi Ohizumi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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