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脱氧尿苷的汞硫类似物对1型和2型单纯疱疹病毒体外复制的抑制作用

Inhibition of herpes simplex virus types 1 and 2 replication in vitro by mercurithio analogs of deoxyuridine.

作者信息

Holliday J, Williams M V

机构信息

Department of Medical Microbiology and Immunology, Ohio State University, Columbus 43210.

出版信息

Antiviral Res. 1991 Sep;16(2):197-203. doi: 10.1016/0166-3542(91)90025-m.

Abstract

The in vitro antiviral activity of several 5-mercurithio analogs of 2'-deoxyuridine (dUrd) on the replication of herpes simplex virus types 1 (HSV-1) and 2 (HSV-2) were examined. Of those compounds tested, the thioglycerol analog of 5-mercuri-2'-deoxyuridine (HgdUrd) was most effective in inhibiting the replication of HSV-1 in KB cells with a 50% inhibitory dose (ID50) of 0.001 micrograms/ml while the glutathione analog of HgdUrd was the most effective in inhibiting the replication of HSV-2 with a ID50 of 0.075 micrograms/ml. Conversely in HeLa TK- cells, the mercaptoguanosine analog of HgdUrd was the most effective compound in inhibiting virus replication with ID50S of 0.098 and 0.001 micrograms/ml for HSV-1 and HSV-2 respectively. These results suggest that these mercurithio analogs of dUrd are as effective as acyclovir in preventing the replication of these herpesviruses.

摘要

研究了几种2'-脱氧尿苷(dUrd)的5-巯基汞类似物对1型单纯疱疹病毒(HSV-1)和2型单纯疱疹病毒(HSV-2)复制的体外抗病毒活性。在所测试的那些化合物中,5-汞-2'-脱氧尿苷(HgdUrd)的硫代甘油类似物在抑制KB细胞中HSV-1复制方面最有效,其50%抑制剂量(ID50)为0.001微克/毫升,而HgdUrd的谷胱甘肽类似物在抑制HSV-2复制方面最有效,ID50为0.075微克/毫升。相反,在HeLa TK-细胞中,HgdUrd的巯基鸟苷类似物是抑制病毒复制最有效的化合物,对HSV-1和HSV-2的ID50分别为0.098和0.001微克/毫升。这些结果表明,这些dUrd的巯基汞类似物在预防这些疱疹病毒复制方面与阿昔洛韦一样有效。

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