Herrmann E C
Appl Microbiol. 1968 Aug;16(8):1151-5. doi: 10.1128/am.16.8.1151-1155.1968.
Herpes simplex and vaccinia viruses and adenovirus types 1, 2, 5, and 7 were tested by plaque suppression methods for sensitivity to halogenated deoxyuridines (5-iodo-, 5-bromo-, 5-chloro-, and 5-fluoro-), cytosine arabinoside, isatin-beta-thiosemicarbazone, and N-methylisatin-beta-thiosemicarbazone. After incubation for 12 days in HeLa cell cultures, vaccinia virus plaques were still readily suppressed by deoxyribonucleic acid (DNA) inhibitors and thiosemicarbazones. Herpes simplex virus plaques were likewise suppressed by at least three DNA inhibitors. Adenovirus plaques were not suppressed by DNA inhibitors or thiosemicarbazones. 5-Fluoro-2'-deoxyuridine could not be shown to have any antiviral activity, but it did produce a substantial lethal action on the cells.
采用蚀斑抑制法检测单纯疱疹病毒、痘苗病毒以及1型、2型、5型和7型腺病毒对卤代脱氧尿苷(5-碘代、5-溴代、5-氯代和5-氟代)、阿糖胞苷、异烟肼-β-硫代半卡巴腙和N-甲基异烟肼-β-硫代半卡巴腙的敏感性。在HeLa细胞培养物中孵育12天后,痘苗病毒蚀斑仍很容易被脱氧核糖核酸(DNA)抑制剂和硫代半卡巴腙抑制。单纯疱疹病毒蚀斑同样被至少三种DNA抑制剂抑制。腺病毒蚀斑未被DNA抑制剂或硫代半卡巴腙抑制。5-氟-2'-脱氧尿苷未显示出任何抗病毒活性,但它对细胞产生了显著的致死作用。