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56.37,56,75,56,75,64.32,71.60,75.68,75.80,78.01,95.64,104.41,104.56,106.71,111.42,114.91,115.38,116.01,116.01,116.41,122.69,124.25,126.45,127.50,132.14,132.14,134.77,135.09,136.93,146.90,147.10,149.32,150.68,158.56,158.85,161.51,162.62,168.75,178.87

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1 .     kaempferol 3-O-(3''-O-E-p-coumaroyl)-(6''-O-E-feruloyl)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:75%
Journal of Natural Products          1999          62          70-75
Acylated Flavonol Glycosides from Leaves of Stenochlaena palustris
Hongmei Liu, Jimmy Orjala, Otto Sticher, and Topul Rali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     stenopalustroside B
C40H34O16     ÏàËÆ¶È:70%
Journal of Natural Products          1999          62          70-75
Acylated Flavonol Glycosides from Leaves of Stenochlaena palustris
Hongmei Liu, Jimmy Orjala, Otto Sticher, and Topul Rali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     quercetin-3-O-(6''-feruloyl)-sophoroside
C37H38O20     ÏàËÆ¶È:69.2%
Phytochemistry          2001          57          1259-1262
Acylated flavonoid glycosides from Bassia muricata
Mohamed S. Kamel, Khaled M. Mohamed, Hashim A. Hassanean,Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     madreselvin B
C36H36O20     ÏàËÆ¶È:69.2%
Journal of Natural Products          1997          60          449-452
Three New Flavonoids and Other Constituents from Lonicera implexa
Guido Flamini, Alessandra Braca, Pier Luigi Cioni, and Ivano Morelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     kaempferol 3-O-[2''-O-(E-6'''-O-feruloyl)-¦Â-D-glucopyranosyl]-¦Â-D-galactopyranoside
C37H38O19     ÏàËÆ¶È:69.2%
Planta Medica          2000          66          374-377
A New Acylated Flavonol Glycoside and Antioxidant Effects of Hedyotis diffusa
Chai-Ming Lu,Jenq-Jer Yang,Phen-Yuh Wang,Chun-Ching Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     Kaempferol-3-O-[6(Glc)-O-feruloyl]-¦Â-D-glucopyranosyl-(1¡ú2)-O-[¦Á-L-rhamnopyranosyl-(1¡ú6)]-¦Â-D-galactopyranoside
C43H48O23    ÏàËÆ¶È:68.2%
Phytochemical Analysis          2000          11          29-33
A novel acylated flavonol glycoside isolated from Brunfelsia grandiflora ssp. grandiflora. Structure elucidation by gradient accelerated NMR spectroscopy at 14T
Gerhard Brunner, Ulrich Burger, Pierre Castioni, Ilias Kapetanidis and Philippe Christen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Kaempferol-3-O-¦Â-D-(2-feruloylglucopyranosyl)(1¡ú 6)-[¦Â-D-glucopyranosyl(1¡ú2)]-¦Â-D-glucopyranoside
C43H48O24     ÏàËÆ¶È:68.2%
Journal of Asian Natural Products Research          2012          14          805-810
A new acylated flavonol glycoside from the aerial parts of Cardamine tangutorum
Wei-Sheng Feng, Qiu-Bo Zhang, Xiao-Ke Zheng, Hui Chen, Yan-Li Zhang & Chun-Lei Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     isorhamnetin 3-O-(6''-O-E-feruloyl)neohesperidoside
C38H40O19     ÏàËÆ¶È:66.6%
Phytochemistry          2006          67          1390-1394
Secondary metabolites from Opuntia ficus-indica var. saboten
Muhammad Saleem, Hyoung Ja Kim, Chang Kyun Han, Changbae Jin,Yong Sup Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     quercetin-3-O-(6''-caffeoyl)-sophoroside
C36H36O20     ÏàËÆ¶È:66.6%
Phytochemistry          2001          57          1259-1262
Acylated flavonoid glycosides from Bassia muricata
Mohamed S. Kamel, Khaled M. Mohamed, Hashim A. Hassanean,Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     isorhamnetin 3-[3'"-feruloylrhamnosyl(1v6)galactoside]
C38H40O19     ÏàËÆ¶È:66.6%
Phytochemistry          1996          41          989-990
An acylated isorhamnetin glycoside from Herniaria fontanesii
Addi Nait Mbark, Dominique Guillaume, Yahia Cherrah, Jean Michel Wieruszeki, Guy Ricart, Zoubida Charrouf
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     kaempferol 3-O-[(6''''-feruloyl)-¦Â-D-glucopyranosyl-(1¡ú3)]-[¦Á-L-rhamnopyranosyl-(1¡ú6)]-¦Â-D-glucopyranoside
C43H48O23    ÏàËÆ¶È:65.8%
Journal of Asian Natural Products Research          2006          8          9-13
A new acylated flavonol glycoside from Derris triofoliata
LU-RONG XU, JUN WU and SI ZHANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     3-O-{2-O-[(E)-caffeoyl]-¦Á-L-arabinopyranosyl-(1¡ú2)-¦Â-D-galactopyranosyl}kaempferol
C35H34O18     ÏàËÆ¶È:64.1%
Helvetica Chimica Acta          2007          Vol. 90          1940
Flavonoid Glycosides from Ranunculus chinensis Bge.
Yan-Ping Zou, Chang-Heng Tan, Bao-De Wang, Shan-Hao Jiang, and Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     kaempferol 3-O-(3'',6''-di-O-E-p-coumaroyl)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:64.1%
Journal of Natural Products          1999          62          70-75
Acylated Flavonol Glycosides from Leaves of Stenochlaena palustris
Hongmei Liu, Jimmy Orjala, Otto Sticher, and Topul Rali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     Turformosin A
C39H40O12     ÏàËÆ¶È:64.1%
Molecules          2012          17          1837-1851
Cytotoxic Phenylpropanoids and a New Triterpene,Turformosinic Acid, from Turpinia formosana Nakai
Hui-Chi Huang,Chun-Tang Chiou, Ping-Chun Hsiao,Chia-Ching Liaw ,Li-Jie Zhang,Chao-Lin Chang,Ih-Sheng Chen, Wen-Chi Chen ,Kuo-Hsiung Lee and Yao-Haur Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     brainoside B
C36H36O20     ÏàËÆ¶È:64.1%
Chemical & Pharmaceutical Bulletin          2010          58          868-871
Phenolic Constituents from Brainea insignis
Kou Wang, Ming-Ming Li, Xuan-Qin Chen, Li-Yan Peng, Xiao Cheng, Yan Li and Qin-Shi Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     brainoside C
C36H36O18     ÏàËÆ¶È:64.1%
Chemical & Pharmaceutical Bulletin          2010          58          868-871
Phenolic Constituents from Brainea insignis
Kou Wang, Ming-Ming Li, Xuan-Qin Chen, Li-Yan Peng, Xiao Cheng, Yan Li and Qin-Shi Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     kaempferol-3-O-[2'',6''-di-(E)-p-coumaroyl]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:64.1%
Journal of Shenyang Pharmaceutical University          2010          27          357-360
Isolation and identification of chemical constituents from leaves of Camellia pitardii Coh. St
SHI Hai-feng, FENG Bao-min, SHI Li-ying, TANG Ling, HOU Lei, WANG Yong-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     É½èÍ·Ó-3-O-(2'',6''-¶þ-O-·´Ê½¶ÔôÇ»ù¹ðƤõ£»ù)-¦Â-D-ÆÏÌÑÌÇÜÕ
    ÏàËÆ¶È:64.1%
Journal of Shenyang Pharmaceutical University          2010          27          292-294
Chemical constituents of leaves from Camellia oleifera Abel
CHEN Yue-long, FENG Bao-min, TANG Ling, LI Hong-bing, SHI Li-ying, WANG Yong-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     Quercetin 3-O-¦Â-D-glucopyranoside-7-O-(6-E-pcoumaroyl)-¦Â-D-glucopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranoside
C42H46O23     ÏàËÆ¶È:62.5%
Fitoterapia          2010          81          940-947
New flavonol glycosides from Aconitum burnatii G¨¢yer and Aconitum variegatum L.
Sara Vitalini, Alessandra Braca, Daniele Passarella, Gelsomina Fico
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     quercetin-3-O-(2-t-p-coumaroyl)-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside-7-O-¦Â-D-glucopyranoside
C42H46O24     ÏàËÆ¶È:61.9%
Fitoterapia          2004          75          533-538
A new acylated quercetin glycoside from Ranunculus lanuginosus
Jos¨¨ Maria Prieto , Alessandra Braca, Ivano Morelli ,Alison Barker, Urs Schaffner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-10-29 14:03:46
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