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4-(N-乙酰氨基)-3-(4-芳基噻唑-2-氨基)苯甲酸乙酯的合成与生物活性
引用本文:夏林,胡艾希,彭俊梅.4-(N-乙酰氨基)-3-(4-芳基噻唑-2-氨基)苯甲酸乙酯的合成与生物活性[J].有机化学,2010,30(4):558-563.
作者姓名:夏林  胡艾希  彭俊梅
作者单位:湖南大学化学化工学院,长沙,410082
基金项目:国家科技支撑计划2006BAE01A01-4资助.
摘    要:以3-氨基-4-乙酰氨基苯甲酸乙酯为原料设计合成了18种4-(N-乙酰氨基)-3-(4-芳基噻唑-2-基)-苯甲酸乙酯新化合物.化合物结构经质谱,元素分析,1H NMR和13C NMR确证.生物活性实验结果表明,化合物3d,3h,3p(40μg/mL)对神经氨酸酶(NA)的抑制率分别为36.02%,33.40%,42.05%;化合物3g,3h(500mg/L)对纹枯病菌的抑制率为50%.

关 键 词:4-(N-乙酰氨基)-3-(4-芳基噻唑-2-氨基)苯甲酸乙酯  神经氨酸酶  合成  生物活性
收稿时间:2009-08-06
修稿时间:2009-11-15

Synthesis and Biological Activity of Ethyl4-Acetamido-3-(4-arylthiazol-2-yl-amino)benzoate
Xia Lin,Hu Aixi,Peng Junmei.Synthesis and Biological Activity of Ethyl4-Acetamido-3-(4-arylthiazol-2-yl-amino)benzoate[J].Chinese Journal of Organic Chemistry,2010,30(4):558-563.
Authors:Xia Lin  Hu Aixi  Peng Junmei
Institution:College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082)
Abstract:A series of ethyl 4-acetamido-3-(4-arylthiazol-2-yl-amino)benzoates were synthesized and evaluated for their ability to inhibit neuraminidase (NA). Their structures were clearly established by MS, elemental analysis, 1H NMR and 13C NMR techniques. The inhibition rates of three compounds 3d, 3h and 3p against influenza A neuraminidase were 36.02%, 33.40% and 42.05% respectively at 40 μg/mL. Compounds 3g and 3h showed fungicidal activity against R. solani with 50% inhibition rate at 500 mg/L.
Keywords:ethyl 4-acetamido-3-(4-arylthiazol-2-yl-amino)benzoate  synthesis  neuraminidase  biological activity
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