کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1393888 | 1501108 | 2016 | 11 صفحه PDF | دانلود رایگان |
• A iconic dual Inhibitor of the wild-Type and drug-resistant mutant of the Influenza A Virus was discovered.
• Structure-activity relationship studies on imidazole-linked pinanamine derivatives were conducted.
• Compound 33 was a highly potent agent against amantadine-resistant influenza virus.
We previously reported potent hit compound 4 inhibiting the wild-type influenza A virus A/HK/68 (H3N2) and A/M2-S31N mutant viruses A/WS/33 (H1N1), with its latter activity quite weak. To further increase its potency, a structure-activity relationship study of a series of imidazole-linked pinanamine derivatives was conducted by modifying the imidazole ring of this compound. Several compounds of this series inhibited the amantadine-sensitive virus at low micromolar concentrations. Among them, 33 was the most potent compound, which was identified as being active on an amantadine-sensitive virus through blocking of the viral M2 ion channel. Furthermore, 33 markedly inhibited the amantadine-resistant virus (IC50 = 3.4 μM) and its activity increased by almost 24-fold compared to initial compound, with its action mechanism being not M2 channel mediated.
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Journal: European Journal of Medicinal Chemistry - Volume 108, 27 January 2016, Pages 605–615