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[纺锤菌素和偏端霉素衍生物对1型单纯疱疹病毒及痘苗病毒的抗病毒特性]

[Antiviral properties of the derivatives of netropsin and distamycin against herpes simplex viruses type 1 and variolovaccine].

作者信息

Andronova V L, Grokhovskiĭ S L, Galegov G A, Deriabin P G, Gurskiĭ G V, L'vov D K

出版信息

Vopr Virusol. 2010 Nov-Dec;55(6):24-7.

Abstract

The antiherpesvirus activity of newly synthesized DNA-binding compounds for cultured Vero E6 cells was examined. The compounds were found to have selective antiherpesviral activity. Their antiviral activity was shown against the virus strains isolated from clinical specimens. The test compounds were ascertained to have also a high activity against herpes simplex virus type 1 (HSV-1/L2 TC-) that was very resistant to acyclovir. The authors' data demonstrated an obvious dose-dependent antiviral effect, which was representatively seen when Pt-bis-Dst and Lys-bis-Nt were used. The findings have offered the challenge to test some of these compounds in experiments on laboratory animals.

摘要

检测了新合成的DNA结合化合物对培养的非洲绿猴肾细胞(Vero E6)的抗疱疹病毒活性。发现这些化合物具有选择性抗疱疹病毒活性。它们对从临床标本中分离出的病毒株具有抗病毒活性。经测定,受试化合物对阿昔洛韦耐药的1型单纯疱疹病毒(HSV-1/L2 TC-)也具有高活性。作者的数据表明存在明显的剂量依赖性抗病毒作用,使用铂-双-去铁胺(Pt-bis-Dst)和赖氨酸-双-新噻吨(Lys-bis-Nt)时可典型地观察到这种作用。这些发现为在实验动物实验中测试其中一些化合物带来了挑战。

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