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Tetrazole and triazole as bioisosteres of carboxylic acid: Discovery of diketo tetrazoles and diketo triazoles as anti-HCV agents

机译:四唑和三唑作为羧酸的生物等排体:二酮四唑和二酮三唑作为抗HCV药物的发现

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A series of diketo tetrazoles and diketo triazoles were designed and synthesized as bioisosteres of α,γ-diketo acid, the active site inhibitor of HCV (Hepatitis C virus) polymerase NS5B. Among the synthesized compounds, 4-(4-fluorobenzyloxy)phenyl diketo triazole (30) exhibited anti-HCV activity with an EC50 value of 3.9 μM and an SI value more than 128. The reduction of viral protein and mRNA levels were also validated, supporting the anti-HCV activity of compound 30. These results provide convincing evidence that the diketo tetrazoles and diketo triazoles can be developed as bioisosteres of α,γ-diketo acid to exhibit potent inhibitory activity against HCV.
机译:设计并合成了一系列二酮四唑和二酮三唑,它们是HCV(丙型肝炎病毒)聚合酶NS5B的活性位点抑制剂α,γ-二酮酸的生物等排体。在合成的化合物中,4-(4-氟苄氧基)苯基二酮三唑(30)表现出抗HCV活性,EC50值为3.9μM,SI值大于128。病毒蛋白和mRNA水平的降低也得到了验证,支持化合物30的抗HCV活性。这些结果提供了令人信服的证据,表明二酮四唑和二酮三唑可以开发为α,γ-二酮酸的生物等排体,表现出对HCV的有效抑制活性。

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