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取代的5-氨基-4-氰基吡唑对脑心肌炎病毒的体外作用模式。

Mode of action in vitro against mengovirus of substituted 5-amino-4-cyanopyrazoles.

作者信息

Tonew M, Lippmann E, Willitzer H

出版信息

Antimicrob Agents Chemother. 1976 Mar;9(3):371-4. doi: 10.1128/AAC.9.3.371.

Abstract

Substituted amino pyrazoles were found to exhibit plaque reduction and inhibition of the cytopathic effect of mengovirus on FL cells. Their antiviral activity was not caused by a virucidal effect or by inhibition of viral adsoprtion or penetration but by suppression of the virus multiplication. During a one-step growth cycle maximum suppression of virus yield occurred after compound addition from 0 to 2 h after infection. Progressively less viral inhibition appeared when compound was applied during the later part of virus replication. The antiviral effect was reversible by removal of the compound, and no inhibitor-resistant period occurred.

摘要

发现取代氨基吡唑具有减少噬斑以及抑制脑心肌炎病毒对FL细胞致细胞病变效应的作用。它们的抗病毒活性并非由杀病毒效应、抑制病毒吸附或穿透所引起,而是由抑制病毒增殖导致的。在一步生长周期中,在感染后0至2小时添加化合物后,病毒产量受到最大程度的抑制。当在病毒复制后期应用化合物时,病毒抑制作用逐渐减弱。去除化合物后,抗病毒作用是可逆的,并且未出现抑制剂抗性期。

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