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À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2014-04-06 18:56:49
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À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2014-04-06 18:56:49
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²éѯ½á¹û£º¹²²éµ½409¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . millepachine C22H22O4 ÏàËÆ¶È:86.3% Fitoterapia 2012 83 1402-1408 Cytotoxic and apoptotic effects of constituents from Millettia pachycarpa Benth Haoyu Ye, Afu Fu, Wenshuang Wu, Yanfang Li, Guangcheng Wang, Minghai Tang, Shucai Li, Shichao He, Shijie Zhong, Huijun Lai, Jianhong Yang, Minli Xiang, Aihua Peng, Lijuan Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 3,6-dimethoxy-6,6-dimethylchromene-(7,8,2,3)flavone ÏàËÆ¶È:59.0% Fitoterapia 2000 71 211-212 Constituents of Bowdichia virgilioides A.M.C. Arriaga, G.A. Gomes, R. Braz-Filho Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . lonchocarpene C21H22O3 ÏàËÆ¶È:59.0% Journal of Natural Products 1986 Vol 49 281 Lonchocarpene, a Stilbene, and Lonchocarpusone, an Isoflavone: Two New Pyranopolyphenols from Lonchocarpus nicou Roots Mourad Kaouadji, Amegninou Agban, Anne-Marie Mariotte, Michel Tissut Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3,6-dimethoxy-6'',6''-dimethylchromeno-(2'',3'':7,8)-flavone ÏàËÆ¶È:59.0% Acta Pharmaceutica Sinica 2006 Vol 41 533-536 Two new flavones from Fordia cauliflora of Yunnan LIANG Zhi-yuan; YANG Xiao-sheng; ZHU Hai-yan; HAO Xiao-jiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 2',3-dihydroxy-4'-methoxy-3'',3''-dimethyl-pyrano[2'',3'':7,8]isoflavanone C21H20O6 ÏàËÆ¶È:59.0% Bioorganic & Medicinal Chemistry 2010 18 962-970 Phenolics from Glycyrrhiza glabra roots and their PPAR-¦Ã ligand-binding activity Minpei Kuroda, Yoshihiro Mimaki, Shinichi Honda, Hozumi Tanaka, Shinichi Yokota, Tatsumasa Mae Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 3,6-dimethoxy-6'',6''-dimethylchromeno-(7,8,2'',3'')-flavone ÏàËÆ¶È:59.0% Natural Product Research and Development 2006 18 55-57 Chemical Constituents of Glechoma longituba ZHANG Qian-jun; YANG Xiao-sheng; ZHU Hai-yan; YAO Yun; HAO Xiao-jiang; SONG Bao-an Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3,6-bis-(4-methoxyphenyl)-4-phenyl-pyran-2-one ÏàËÆ¶È:59.0% Bioorganic & Medicinal Chemistry 2009 17 3847-3856 Synthesis and biological evaluation of 3,4,6-triaryl-2-pyranones as a potential new class of anti-breast cancer agents Ravi Shankar, Bandana Chakravarti, Uma Sharan Singh, Mohd. Imran Ansari, Shreekant Deshpande, Shailendra Kumar Dhar Dwivedi, Hemant Kumar Bid, Rituraj Konwar, Geetika Kharkwal, Vishal Chandra, Anila Dwivedi, K. Hajela Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 3,30-((6,7-dimethoxyquinazoline-2,4-diyl)bis(azanediyl))-dibenzonitrile C24H18N6O2 ÏàËÆ¶È:59.0% Bioorganic & Medicinal Chemistry 2013 21 7858-7873 Investigation of quinazolines as inhibitors of breast cancer resistance protein (ABCG2) Kapil Juvale, Jennifer Gallus, Michael Wiese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 4p C32H29ClN2O7 ÏàËÆ¶È:59.0% Tetrahedron 2012 68 8256-8260 Efficient synthesis of pentasubstituted pyrroles via one-pot reactions of arylamines, acetylenedicarboxylates, and 3-phenacylideneoxindoles Ying Han, Yan Sun, Jing Sun, Chao-Guo Yan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (E)-2',5'-¶þ¼×Ñõ»ù-3,4-(2,2-¶þ¼×»ùßÁà«)-2-ôÇ»ù²é¶ûͪ C22H22O5 ÏàËÆ¶È:59.0% Chinese Journal of Organic Chemistry 2013 33 159-163 A Concise Synthesis of Barbigerone and Structural Analogues Yang Youzhe, Wang Chao, Sun Jian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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