Study of the Antiviral Activity of Adamantane-Containing Chemical Compounds

I. I. Lyubimov, E. Isaeva, E. Vetrova, A. Lavrova, N. Gretskaya, I. Serkov, V. Bezuglov, G. Galegov
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引用次数: 1

Abstract

Influenza and coronavirus infections are especially dangerous due to being capable of causing pandemics and clinical complications in the nervous and cardiovascular systems, as well as exacerbation of chronic diseases (diabetes mellitus, heart failure, chronic obstructive bronchopneumonia, etc.), which can cause delayed death, especially in children under two years of age, the elderly, and individuals with poor health. The aim of the study was to search for compounds effective against these two topical viruses which possess constant epidemic activity - influenza virus and betacoronavirus - among new adamantane derivatives containing a NO-donor fragment or a dopamine residue. Another purpose of the study was determination of cytotoxicity and antiviral activity of compounds on cell lines permissive for influenza virus and betacoronavirus. The antiviral activity of 6 adamantane derivatives against strains of the influenza virus (H1N1) and betacoronavirus was studied. It was established that the NO-donor derivative of aminoadamantane succinate and the dopamine derivative of adamantanebenzoic acid had the greatest ability to suppress the development of the influenza virus with a chemotherapeutic index above 60. No promising compounds against betacoronavirus were identified.
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含金刚烷类化合物抗病毒活性的研究
流感和冠状病毒感染尤其危险,因为它们能够引起大流行和神经系统和心血管系统的临床并发症,以及慢性疾病(糖尿病、心力衰竭、慢性阻塞性支气管肺炎等)的恶化,这可能导致延迟死亡,特别是在两岁以下儿童、老年人和健康状况不佳的个人中。该研究的目的是在含有no供体片段或多巴胺残基的新型金刚烷衍生物中寻找对具有持续流行活性的两种局部病毒(流感病毒和乙型冠状病毒)有效的化合物。该研究的另一个目的是确定流感病毒和乙型冠状病毒允许的细胞系上化合物的细胞毒性和抗病毒活性。研究了6种金刚烷衍生物对甲型H1N1流感病毒和乙型冠状病毒的抗病毒活性。结果表明,氨基金刚烷琥珀酸no供体衍生物和金刚烷苯甲酸多巴胺衍生物对流感病毒的抑制能力最强,化疗指数均在60以上。没有发现有希望的抗冠状病毒化合物。
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