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²éѯ½á¹û£º¹²²éµ½300¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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