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-------------------------------------------------------------------------------- 1 . 5,7-dihydroxychromone C9H6O4 ÏàËÆ¶È:69.2% China Journal of Chinese Materia Medica 2008 33 1218-1220 Flavonoids from Aerial Parts of Arachniodes exilis ZHOU Daonian, RUAN Jinlan, CAI Yaling Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 5,7-dihydroxy-4H-4-chromenone ÏàËÆ¶È:69.2% China Journal of Chinese Materia Medica 2006 31 468-471 Non-alkaloid constituents from a Tibetan medicine Meconopsis quintuplinervia SHANG Xiaoya, LI Chong, ZHANG Chengzhong, YANG Yongchun, SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 5,7-dihydroxychromone ÏàËÆ¶È:69.2% Acta Pharmaceutica Sinica 2008 Vol 43 388-391 A new triterpenoid saponin from the fruits of Polygonum orientale YANG Zhi-yun; QIAN Shi-hui; QIN Min-jian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 5,7-dihydroxychromone ÏàËÆ¶È:69.2% China Journal of Chinese Materia Medica 2010 35 3302-3305 Chemical constituents from flowers of Chrysanthemum indicum FENG Ziming; YANG Yanan; JIANG Jianshuang; ZHANG Peicheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 5,7-dihydroxychromone ÏàËÆ¶È:69.2% Chinese Pharmaceutical Journal 2008 43 1218-1220 Flavonoids from Aerial Parts of Arachniodes exilis ZHOU Dao-nian, RUAN Jin-lan, CAI Ya-ling Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . genistein ÏàËÆ¶È:61.5% Food Chemistry 2012 131 161-169 Changes occurring in compositional components of black soybeans maintained at room temperature for different storage periods Jin Hwan Lee, Kye Man Cho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . genistein ÏàËÆ¶È:61.5% Food Chemistry 2009 114 869-873 Isolation and characterisation of the isoflavones from sprouted chickpea seeds Shuhui Zhao, Linping Zhang, Peng Gao, Zhiyu Shao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Genistein ÏàËÆ¶È:61.5% Journal of Agricultural and Food Chemistry 1994 42 1869-1871 Microwave-Mediated Synthesis of Anticarcinogenic Isoflavones from Soybeans Yu-Chen Chang, Muraleedharan G. Nair, Ross C. Santell, William G. Helferich Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 5,7,2',6'-Tetrahydroxyflavone C15H10O6 ÏàËÆ¶È:60% Chemistry of Natural Compounds 2002 38 358-406 PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria L. GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES V. M. Malikov and M. P. Yuldashev Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 2',4',5,7-Tetrahydroxyisoflavone ÏàËÆ¶È:60% Archives of Pharmacal Research 2004 27 544-546 Flavonoids of crotalaria sessiliflora Hun Sung Yoo, Ji Suk Lee, Chul Young Kim and Jinwoong Kim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 5,7,2',4'-tetrahydroxy-3-methoxyflavone C16H12O7 ÏàËÆ¶È:56.2% Chinese Chemical Letters 2008 19 196-198 A new benzofuranolignan and a new flavonol derivative from the stem of Morus australis Qing Jian Zhang, Di Zao Li, Ruo Yun Chen, De Quan Yu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 5,6',7-trihydroxy-3',4'-methylenedioxyisoflavone ÏàËÆ¶È:56.2% Bulletin of the Korean Chemical Society 2004 25 147-148 New Isoflavone Glycoside from the Woods of Sophora japonica Youngki Park*, Hak-Ju Lee, Sung-Suk Lee, Don-Ha Choi, Jung-Soo Oh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 5,7,2',4'-tetrahydroxy-3-methoxyflavone C16H12O7 ÏàËÆ¶È:56.2% Zeitschrift f¨¹r Naturforschung C 2008 63 35-39 Phenolic Constituents from the Wood of Morus australis with Cytotoxic Activity Ferlinahayati, Y. M. Syah, L. D. Juliawaty, S. A. Achmad, E. H. Hakim, H. Takayama, I. M. Said, and J. Latip Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 5,7-dihydroxy-3',5'-dimethoxyflavone C17H14O6 ÏàËÆ¶È:53.8% Journal of Natural Products 2003 66 1273-1275 Tricin from a Malagasy Connaraceous Plant with Potent Antihistaminic Activity Hidenori Kuwabara,Kyoko Mouri, Hideaki Otsuka,Ryoji Kasai, and Kazuo Yamasaki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 5,7-dihydroxy-3',5'-dinitroflavone C15H8O8N2 ÏàËÆ¶È:53.8% Journal of Natural Products 2003 66 1273-1275 Tricin from a Malagasy Connaraceous Plant with Potent Antihistaminic Activity Hidenori Kuwabara,Kyoko Mouri, Hideaki Otsuka,Ryoji Kasai, and Kazuo Yamasaki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . chrysin ÏàËÆ¶È:53.8% Chemical & Pharmaceutical Bulletin 1989 37 3128-3130 Isolation of Flavonoids from Populus nigra as ¦¤4-3-Ketosteroid (5¦Á) Reductase Inhibitors Yasuo KOMODA Structure 13C NMR ̼Æ×Ä£Äâͼ |

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