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[异头碳5-取代-2'-脱氧尿苷的抗病毒活性]

[Antiviral activity of anomeric 5-substituted 2'-deoxyuridines].

作者信息

Bektemirov T A, Chekunova E V, Andzhaparidze O G, Mel'nik S Ia, Bakhmedova A A

出版信息

Vopr Virusol. 1979 Nov-Dec(6):603-6.

PMID:524857
Abstract

The inhibiting effect for herpes and vaccinia viruses of 2'-deoxyuridine derivatives containing the substitute in the position of 5-pyrimidine ring was studied. Anomeric 5-isopropyl-2'-deoxyuridines were shown to produce a marked inhibiting effect in chick embryo fibroblasts infected with herpes virus and to have no effect on vaccinia virus replication, that is, to be specific antiherpetic agents. The alpha-anomer of 5-isopropyl-2'-deoxyuridine showed antiherpetic activity in vitro comparable with that of beta-anomer. Fifty per cent toxic doses and chemotherapeutic indices of the drugs under study were determined in comparison with those of 5-iod-2'-deoxyuridine.

摘要

研究了在5-嘧啶环位置含有取代基的2'-脱氧尿苷衍生物对疱疹病毒和痘苗病毒的抑制作用。结果表明,异头型5-异丙基-2'-脱氧尿苷对感染疱疹病毒的鸡胚成纤维细胞有显著抑制作用,而对痘苗病毒复制无影响,即具有特异性抗疱疹作用。5-异丙基-2'-脱氧尿苷的α-异头体在体外显示出与β-异头体相当的抗疱疹活性。与5-碘-2'-脱氧尿苷相比,测定了所研究药物的半数毒性剂量和化疗指数。

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