کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1392446 | 1501133 | 2014 | 8 صفحه PDF | دانلود رایگان |
• Pyrimidine ring shows a wide variety of pharmacological properties.
• 6-Oxo-1,4,5,6-tetrahydropyrimidine compounds were found to be a new class of potential anti-influenza agents.
• Evaluate their ability of inhibiting neuraminidase (NA) of influenza A virus.
• Compound 6g exhibited the strongest inhibitory activity against influenza virus A NA (IC50 = 17.64 μM).
• Molecular modeling was applied to illustrate compound interactive with proteins.
A series of 6-oxo-1,4,5,6-tetrahydropyrimidine-5-carboxylate derivatives were prepared to evaluate their ability of inhibiting neuraminidase (NA) of influenza A virus. All the compounds were synthesized in good yields starting from aldehyde by using a suitable synthetic strategy, which showed moderate inhibitory activity against influenza A NA. Compound 6g exhibited the strongest inhibitory activity against influenza virus A NA (IC50 = 17.64 μM), which indicated pyrimidine ring could be used as a core structure to design novel influenza NA inhibitors.
A series of 6-oxo-1,4,5,6-tetrahydropyrimidine-5-carboxylate derivatives were prepared. Most of them have moderate NA inhibitory activity which indicated pyrimidine ring could be used as a core structure to design novel influenza NA inhibitors.Figure optionsDownload as PowerPoint slide
Journal: European Journal of Medicinal Chemistry - Volume 83, 18 August 2014, Pages 466–473