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松香基脲类衍生物的合成及其抗菌活性研究
引用本文:廖迎,李芳耀,黄凤香. 松香基脲类衍生物的合成及其抗菌活性研究[J]. 华夏医学, 2007, 20(2): 209-211
作者姓名:廖迎  李芳耀  黄凤香
作者单位:桂林医学院药学院,广西,桂林,541004
摘    要:目的:设计合成了一系列松香基脲类衍生物,初步研究了其抗菌活性。方法:以脱氢松香酸为起始原料,酰氯化后,经Curtius重排得到松香基异氰酸酯,然后与芳香胺反应得到松香基脲。结果:得到5个松香基脲类化合物,经IR、1H-NMR、元素分析等确证其结构。结论:初步药理实验表明,合成产物对金黄色葡萄球菌及大肠杆菌具有良好的抗菌活性。

关 键 词:脱氢松香酸    Curtius重排  抗菌活性
文章编号:1008-2409(2007)02-0209-03
修稿时间:2007-01-17

Synthesis and antibacterial activity of some urea from dehydroabietic acid
LIAO Ying,LI Fang-yao,HUANG Feng-xiang. Synthesis and antibacterial activity of some urea from dehydroabietic acid[J]. Acta Medicinae Sinica, 2007, 20(2): 209-211
Authors:LIAO Ying  LI Fang-yao  HUANG Feng-xiang
Affiliation:LIAO Ying,LI Fang-yao,HUANG Feng-xiangGuilin Medical College,Guilin 541004,China
Abstract:Objective:To design and synthesize a series of urea derivertives from dehydroabietic acid,and to determine their antibacterial activity.Methods:The urea derivertives were prepared by the acyl chloridate with dehydroabietic acid,Curtius rearrangement and then reaction with aromatic amine.Results:Five dehydroabietylureas were obtained and their structures were characterized by IR,1H-NMR and elemental analysis.Conclusion:Pharmacological tests inducated that these ureas possessed excellent inhibitive activity against S.aureus and E.Colt.
Keywords:dehydroabietic acid  urea  Curtius rearrangement  antibacterial activity
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