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单纯疱疹病毒胸苷激酶的特异性抑制剂可减少潜伏病毒从移植的小鼠神经节中重新激活。

Specific inhibitors of herpes simplex virus thymidine kinase diminish reactivation of latent virus from explanted murine ganglia.

作者信息

Leib D A, Ruffner K L, Hildebrand C, Schaffer P A, Wright G E, Coen D M

机构信息

Laboratory of Tumor Virus Genetics, Dana Farber Cancer Institute, Boston, Massachusetts.

出版信息

Antimicrob Agents Chemother. 1990 Jun;34(6):1285-6. doi: 10.1128/AAC.34.6.1285.

Abstract

Two specific inhibitors of herpes simplex virus thymidine kinase, N2-phenyl-2'-deoxyguanosine and N2-(m-trifluoromethylphenyl)guanine, were tested for their ability to inhibit the reactivation of virus from explant cultures of latently infected murine trigeminal ganglia. Both compounds significantly diminished the frequency of reactivation compared with that of untreated controls.

摘要

对单纯疱疹病毒胸苷激酶的两种特异性抑制剂,即N2-苯基-2'-脱氧鸟苷和N2-(间三氟甲基苯基)鸟嘌呤,进行了测试,以考察它们抑制潜伏感染的小鼠三叉神经节外植体培养物中病毒再激活的能力。与未处理的对照相比,这两种化合物均显著降低了再激活频率。

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Prodrugs of herpes simplex thymidine kinase inhibitors.单纯疱疹胸苷激酶抑制剂的前药。
Antivir Chem Chemother. 2015 Apr;24(2):47-55. doi: 10.1177/2040206615608722. Epub 2015 Oct 13.

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Prodrugs of herpes simplex thymidine kinase inhibitors.单纯疱疹胸苷激酶抑制剂的前药。
Antivir Chem Chemother. 2015 Apr;24(2):47-55. doi: 10.1177/2040206615608722. Epub 2015 Oct 13.

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