Antiviral activity of the novel immune modulator 7-thia-8-oxoguanosine.

D F Smee, H A Alaghamandan, H B Cottam, W B Jolley, R K Robins
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引用次数: 0

Abstract

A novel thiazolopyrimidine nucleoside, 5-amino-3-beta-D-ribofuranosylthiazolo[4,5-d]pyrimidine-2,7(3H,6H) -dione (7-thia-8-oxoguanosine), was evaluated for antiviral activity in rodent models, and at 50-200 mg/kg prevented death in mice inoculated intraperitoneally (i.p.) with Semliki Forest, San Angelo, and banzi viruses when administered i.p. before virus challenge. Similarly, the nucleoside was effective against an intranasal challenge of rat coronavirus in suckling rats, with activity present when treatment started as late as 4 h after virus inoculation. Protection was observed against herpes type 1 and murine cytomegalovirus (both inoculated i.p.) infections, and encephalitis induced by intracerebral inoculation of a human coronavirus in mice. Friend leukemia virus splenomegaly was more severe in drug-treated animals than in placebos. This immune modulator is promising for the treatment of animal and human diseases.

新型免疫调节剂7-thia-8-氧鸟苷的抗病毒活性。
一种新型噻唑嘧啶核苷,5-氨基-3- β -d -核糖呋喃基噻唑[4,5-d]嘧啶-2,7(3H,6H) -二酮(7-噻亚-8-氧鸟苷),在啮齿动物模型中进行了抗病毒活性评估,在病毒攻击前腹腔注射50-200 mg/kg,可预防小鼠腹腔接种塞姆利基森林病毒、圣安吉洛病毒和班齐病毒的死亡。同样,核苷对哺乳大鼠鼻腔内的大鼠冠状病毒攻击有效,在病毒接种后4小时开始治疗时仍有活性。观察到小鼠对1型疱疹病毒和小鼠巨细胞病毒(均接种于腹腔)感染和脑内接种人冠状病毒引起的脑炎具有保护作用。白血病病毒脾肿大在药物治疗组比安慰剂组更严重。这种免疫调节剂有望用于动物和人类疾病的治疗。
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