Wroclaw University of Technology, Division of Medicinal Chemistry and Microbiology, Faculty of Chemistry , Wybrzeze Wyspianskiego 27, 50-370 Wroclaw , Poland +48 71 320 24 39 ; +48 71 320 24 27 ;
Expert Opin Ther Pat. 2014 Aug;24(8):925-41. doi: 10.1517/13543776.2014.927442. Epub 2014 Jul 10.
The standard therapy used to treat herpesvirus infections is based on the application of DNA polymerase inhibitors such as ganciclovir or aciclovir. Unfortunately, all of these compounds exhibit relatively high toxicity and the mutation of herpesviruses results in the appearance of new drug-resistant strains. Consequently, there is a great need for the development of new, effective and safe anti-herpesvirus agents that employ different patterns of therapeutic action at various stages of the virus life cycle.
Patents and patent applications concerning the development of anti-herpesvirus agents displaying different mechanisms of action that have been published since 2003 are reviewed. In addition, major discoveries in this field that have been published in academic papers have also been included.
Among all the anti-herpesvirus agents described in this article, the inhibitors of viral serine protease seem to present one of the most effective/promising therapeutics. Unfortunately, the practical application of these antiviral agents has not yet been proven in any clinical trials. Nevertheless, the dynamic and extensive work on this subject gives hope that a new class of anti-herpesvirus agents aimed at the enzymatic activity of herpesvirus serine protease may be developed.
目前,治疗疱疹病毒感染的标准疗法是基于应用 DNA 聚合酶抑制剂,如更昔洛韦或阿昔洛韦。不幸的是,所有这些化合物都表现出相对较高的毒性,而疱疹病毒的突变导致新的耐药株出现。因此,非常需要开发新的、有效和安全的抗疱疹病毒药物,这些药物在病毒生命周期的各个阶段采用不同的治疗作用模式。
本文综述了自 2003 年以来发表的有关显示不同作用机制的抗疱疹病毒药物的专利和专利申请。此外,还包括该领域在学术论文中发表的主要发现。
在本文描述的所有抗疱疹病毒药物中,病毒丝氨酸蛋白酶抑制剂似乎是最有效/有前途的治疗方法之一。不幸的是,这些抗病毒药物的实际应用尚未在任何临床试验中得到证实。然而,对这一主题的广泛深入研究给人以希望,即可能开发出一类针对疱疹病毒丝氨酸蛋白酶酶活性的新型抗疱疹病毒药物。