RME-based pharmacology: The inhibition of viral entry as therapeutic perspective in viral diseases including AIDS. Hypothesis updated and enlarged

G. Chaldakov, S. Yanev
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引用次数: 1

Abstract

coated pits/vesicles was the best-characterized endocytic pathway. Since then now, intensive research on the mechanisms of both RME and receptor-mediated virus-cell fusion (receptor-mediated fusion - RMF) helped to expand the list of chemical compounds with potential clinical application as antiviral agents, the so-called entry inhibitors, e.g. (i) inhibitors of clathrin-, dynamin-2-, caveolin- and/or lipid rafts-dependent RME, and (ii) inhibitors of RMF. Accordingly, in the present Dance Round we update and enlarge our hypothesis of RME-based antiviral pharmacology. Biomed Rev 2018; 29: 109-118
基于rme的药理学:抑制病毒进入作为包括艾滋病在内的病毒性疾病的治疗观点。更新和扩大假设
包被凹坑/囊泡是最具特征的内吞途径。从那时起,对RME和受体介导的病毒-细胞融合(receptor-mediated fusion - RMF)机制的深入研究有助于扩大具有潜在临床应用的抗病毒药物的化合物列表,即所谓的进入抑制剂,例如(i)网格蛋白-、动力蛋白-2-、小窝蛋白和/或脂质raft依赖的RME抑制剂,以及(ii) RMF抑制剂。因此,在本文中,我们更新并扩大了基于rme的抗病毒药理学假设。Biomed Rev 2018;29日:109 - 118
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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