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13C NMR (151 MHz, CDCl3)£º27.92,55.31,55.74,76.73,76.76,77.01,77.33,103.42,110.38,114.34,116.68,121.85,125.11,128.32,128.57,129.73,131.59,141.28,153.53,158.21,161.11,189.97

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À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2014-04-06 18:56:49
Сºç: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл£¡¸Ð¼¤Ö®ÖÁ£¡ 2014-04-07 11:04:42
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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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ
2Â¥2014-04-06 16:07:39
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