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1 .     6-hydroxy-4',7-dimethoxyisoflavone
C17H14O5     ÏàËÆ¶È:86.6%
Chemical & Pharmaceutical Bulletin          2009          57          346-360
Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities
Hideyuki Goto, Yoshiyasu Terao and Shuji Akai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     4',6-dimethoxy-7-hydroxyisoflavone
    ÏàËÆ¶È:80%
Chemistry of Natural Compounds          2009          45          420-421
ISOLATION AND IDENTIFICATION OF 4¡ä,6-DIMETHOXY-7-HYDROXYISOFLAVONEFROM ROOTS OF Hedysarum theinum CULTIVATED in vitro
I. V. Nechepurenko, N. I. Komarova, I. N. Kuzovkina,M. Yu. Vdovitchenko, M. P. Polovinka,and N. F. Salakhutdinov1
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     7-hydroxy-6,4'-dimethoxyisoflavone
    ÏàËÆ¶È:80%
Phytochemistry          1998          47          117-119
Isoflavonoids and a pterocarpan from Gliricidia sepium
H. M. T. B. Herath, R. S. Dassanayake, A. M. A. Priyadarshani, Susila De Silva, G. P. Wannigama, Joanne Jamie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




4 .     7-hydroxy-4',6-dimethoxyisoflavone
C17H14O5     ÏàËÆ¶È:80%
Chemical & Pharmaceutical Bulletin          2009          57          346-360
Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities
Hideyuki Goto, Yoshiyasu Terao and Shuji Akai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     afrormosin
    ÏàËÆ¶È:80%
Chinese Journal of Natural Medicines          2006          4          151-153
The Anticancer Activity in vitro of Constituents from Fruits of Sophora japonica
MA Lei; LOU Feng-Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     afromosin
    ÏàËÆ¶È:80%
Chinese Pharmaceutical Journal          2009          44          1533-1535
Isoflavonoids from Hedysarum semenovii
LIU Yi, HAI Li-qian, ZHAO Yu-ying, ZHANG Qing-ying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




7 .     afromosin
C17H14O5     ÏàËÆ¶È:80%
Food Chemistry          2011          126          1057-1063
The most abundant polyphenol of soy leaves, coumestrol, displays potent ¦Á-glucosidase inhibitory activity
Heung Joo Yuk, Jin Hwan Lee, Marcus J. Curtis-Long, Ji Won Lee, Young Soo Kim, Hyung Won Ryu, Chung Gyoo Park, Tae-Sook Jeong, Ki Hun Park
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     4',6-dihydroxy-7-methoxyisoflavone
C16H12O5     ÏàËÆ¶È:78.5%
Chemical & Pharmaceutical Bulletin          2009          57          346-360
Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities
Hideyuki Goto, Yoshiyasu Terao and Shuji Akai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




9 .     afromosin
    ÏàËÆ¶È:78.5%
Natural Product Research and Development          2012          24          610-613
Isoflavonoids from Piptanthus concolor Harrow
KOU Zhong-jing; CHANG Rui-jie; QIN Jiang-jiang; YAN Shi-kai; JIN Hui-zi; ZHANG Wei-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     Formononetin
    ÏàËÆ¶È:71.4%
Chemistry of Natural Compounds          2006          42          567-570
NEW THIAZINEDIONES AND OTHER COMPONENTS FROM Xanthium strumarium
Ting Han, Huiliang Li, Qiaoyan Zhang,Hanchen Zheng, and Luping Qin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




11 .     formononetin
    ÏàËÆ¶È:71.4%
China Journal of Chinese Materia Medica          2004          29          434-436
Studies on chemical constituents of Sini Tang
LIU Hongxia, LIN Wenhan, YANG Junshan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




12 .     4',7-dihydroxy-6-methoxyisoflavone
C16H12O5     ÏàËÆ¶È:71.4%
Chemical & Pharmaceutical Bulletin          2009          57          346-360
Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities
Hideyuki Goto, Yoshiyasu Terao and Shuji Akai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




13 .     4',7-dihydroxy-6-methoxyisoflavone
    ÏàËÆ¶È:71.4%
China Journal of Chinese Materia Medica          2010          35          2416-2419
Chemical constituents of bear bile
LUO Qiang; CHEN Quancheng; WU Yao; JIANG Miaomiao; CHEN Zhihong; ZHANG Xiaokun; CHEN Haifeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




14 .     4'-methoxy-7-hydroxyisoflavone
    ÏàËÆ¶È:71.4%
China Journal of Chinese Materia Medica          2010          35          2416-2419
Chemical constituents of bear bile
LUO Qiang; CHEN Quancheng; WU Yao; JIANG Miaomiao; CHEN Zhihong; ZHANG Xiaokun; CHEN Haifeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




15 .     6,7,4,-trihydroxyisoflavone
    ÏàËÆ¶È:71.4%
Bioorganic & Medicinal Chemistry Letters          2008          18          5006-5009
ortho-Dihydroxyisoflavone derivatives from aged Doenjang (Korean fermented soypaste) and its radical scavenging activity
Jun-Seong Park, Hye Yoon Park, Dong Hyun Kim, Duck Hee Kim, Han Kon Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




16 .     6,7,4'-trihydroxyisoflavone
    ÏàËÆ¶È:71.4%
Bioorganic & Medicinal Chemistry Letters          2010          20          1162-1164
Natural ortho-dihydroxyisoflavone derivatives from aged Korean fermented soybean paste as potent tyrosinase and melanin formation inhibitors
Jun-Seong Park, Dong Hyun Kim, Jae Kyoung Lee, Jin Young Lee, Duck Hee Kim, Han Kon Kim, Hak-Ju Lee, Ho Cheol Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




17 .     formonoetin
    ÏàËÆ¶È:71.4%
Chinese Pharmaceutical Journal          2009          44          897-899
Studies on Chemical Constituents of Alhagi pseudalhagi(M.B.)
ZHANG Gui-jie, LI Ning, XIONG Yuan-jun, LI Xian, LI Yong, JIA Xiao-guang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




18 .     4',7-¶þôÇ»ù-6-¼×Ñõ»ùÒì»ÆÍª
    ÏàËÆ¶È:71.4%
Chinese Journal of Medicinal Chemistry          2009          19          375-378
Secondary metabolites from the broth of an alkalophilic streptomycete
ZHENG Dan, JIANG Yi, LOU Kai, CHEN Yun, XU Li-hua, HAN Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




19 .     formononetin
C16H12O4     ÏàËÆ¶È:71.4%
Food Chemistry          2011          126          1057-1063
The most abundant polyphenol of soy leaves, coumestrol, displays potent ¦Á-glucosidase inhibitory activity
Heung Joo Yuk, Jin Hwan Lee, Marcus J. Curtis-Long, Ji Won Lee, Young Soo Kim, Hyung Won Ryu, Chung Gyoo Park, Tae-Sook Jeong, Ki Hun Park
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




20 .     formononetin
    ÏàËÆ¶È:71.4%
Chinese Journal of Natural Medicines          2012          10          0287-0291
Flavanoids from the stems of Aquilaria sinensis
Dong CHEN, Dan BI, Yue-Lin SONG, Peng-Fei TU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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