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1 . 6-hydroxy-4',7-dimethoxyisoflavone C17H14O5 ÏàËÆ¶È:81.2% 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:75% 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 . glycitrin ÏàËÆ¶È:75% China Journal of Chinese Materia Medica 2003 28 43-47 Isolation and Elucidation of Chemical Constituents with Antiviral Action from Yinqiaosan on Influenza Virus SHI Yue, SHI Renbing, LIU Bin, LU Yunru, DU Lijun Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 7-hydroxy-6,4'-dimethoxyisoflavone ÏàËÆ¶È:75% 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 5 . 7-hydroxy-4',6-dimethoxyisoflavone C17H14O5 ÏàËÆ¶È:75% 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 6 . formonoetin ÏàËÆ¶È:75% Fitoterapia 2010 81 1058-1061 New isoflavonolignan with quinone reductase inducing activity from Alhagi pseudalhagi (M.B.) Ning Li, Guijie Zhang, Yuanjun Xiong, Bolat Makhabel, Xian Li, Xiaoguang Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . afrormosin ÏàËÆ¶È:75% 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 8 . compound 3 ÏàËÆ¶È:75% Archives of Pharmacal Research 1991 14 105-108 Insecticidal isoflavon glycoside from Maackia amurensis Hasik Youn, Sangkyun Lee, Jin-Ho Cho and Hunseung Oh Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . formononetin ÏàËÆ¶È:75% Chinese Pharmaceutical Journal 2005 40 1057-1059 Studies on chemical constituents of Trifolium pratense MA Qiang, LEI Hai-min, ZHOU Yu-xin, WANG Chang-hai Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . formononetin ÏàËÆ¶È:75% Chinese Pharmaceutical Journal 2006 41 1217-1221 Studies on Chemical Constituents of Astragalus membranaceus(Fisch.) Bge.var.mongholicus(Bge.) Hsiao BIAN Yun-yun, GUAN Jia, BI Zhi-ming, SONG Yue, LI Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . afromosin ÏàËÆ¶È:75% 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 12 . afromosin C17H14O5 ÏàËÆ¶È:75% 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 13 . formononetin ÏàËÆ¶È:75% Journal of Agricultural and Food Chemistry 2006 54 2057-2063 LDL-Antioxidant Pterocarpans from Roots of Glycine max (L.) Merr. Jin Hwan Lee, Byong Won Lee, Jin Hyo Kim, Tae-Sook Jeong, Min Jung Kim, Woo Song Lee, and Ki Hun Park Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Formononetin C16H12O4 ÏàËÆ¶È:75% Journal of Chinese Pharmaceutical Sciences 2012 21 428-434 Chemical constituents of Pseudolarix kaempferi Gord Tianzhi Cai; Wen Qi; Lianmei Yang; Guangzhong Tu; Rong Yang; Kehui Xie; Hongzheng Fu Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . afrormosin C17H14O5 ÏàËÆ¶È:70.5% Chinese Pharmaceutical Journal 2006 41 1217-1221 Studies on Chemical Constituents of Astragalus membranaceus(Fisch.) Bge.var.mongholicus(Bge.) Hsiao BIAN Yun-yun, GUAN Jia, BI Zhi-ming, SONG Yue, LI Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 8-O-methylretusin ÏàËÆ¶È:70.5% International Journal of Molecular Sciences 2012 13 11349-11364 Phenolic Compounds from Halimodendron halodendron (Pall.) Voss and Their Antimicrobial and Antioxidant Activities Jihua Wang, Jingfeng Lou, Chao Luo, Ligang Zhou, Mingan Wang and Lan Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . formononetin ÏàËÆ¶È:68.7% Planta Medica 1988 54 250-254 Isolation and High Performance Liquid Chromatography (HPLC) of Isoflavonoids from the Pueraria Root Yukio Ohshima, Toru Okuyama, Kunio Takahashi, Toshio Takizawa, and Shoji Shibata Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 7-Hydroxyl-4'-methoxyisoflavone C16H12O4 ÏàËÆ¶È:68.7% Chemistry of Natural Compounds 2007 43 214-215 CHEMICAL RESEARCH OF Caragana microphylla Seeds Yan Huo, Cheng Guo, Shan Lu,Qiao-Yan Zhang, and Lu-Ping Qin Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Formononetin ÏàËÆ¶È:68.7% Chemistry of Natural Compounds 2007 43 614-615 FLAVONOIDS FROM Trifolium resupinatum VAR. microcephalum Emel Isik, Temine Sabudak, and Sevi Oksuz Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Formononetin C16H12O4 ÏàËÆ¶È:68.7% Chemistry of Natural Compounds 2002 38 473-519 PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES V. M. Malikov and M. P. Yuldashev Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Formononetin ÏàËÆ¶È:68.7% Journal of Chinese Pharmaceutical Sciences 2006 15 15-20 Flavanoids from Clematis hexapetala DONG Cai-xia; WU Ke-si; SHI She-po; and TU Peng-fei Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . formononetin ÏàËÆ¶È:68.7% China Journal of Chinese Materia Medica 2003 28 43-53 Isolation and Elucidation of Chemical Constituents with Antiviral Action from Yinqiaosan on Influenza Virus SHI Yue, SHI Renbing, LIU Bin, LU Yunru, DU Lijun Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . formononetin ÏàËÆ¶È:68.7% Acta Pharmaceutica Sinica 2003 Vol 38 592-595 Studies on chemical constituents of Hedysarum polybotrys HAI Li qian; ZHANG Qing ying; LIANG Hong; ZHAO Yu ying; DU Nian sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . Herbacetin 4'-methyl ether C16H12O7 ÏàËÆ¶È:68.7% Phytochemistry 1994 37 455-456 A herbacetin methyl ether from the farinose exudate of a Pentagramma triangularis hybrid Eckhard Wollenweber, Sylvia Armbruster, James N. Roitman Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 4',6-dihydroxy-7-methoxyisoflavone C16H12O5 ÏàËÆ¶È:68.7% 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 26 . 8-hydroxy-4'-methoxy-7-methylisoflavone C17H14O4 ÏàËÆ¶È:68.7% 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 27 . 4',6,7-trimethoxyisoflavone C18H16O5 ÏàËÆ¶È:68.7% 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 |

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