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3-[双-(2-羟乙基)-氨基]-苯乙酮-[4,5-二苯基-恶唑基-(2)]-腙(IMET 98/69)对致死性门戈病毒脑炎的作用

Effect of 3-[bis-(2-hydroxyethyl)-amino]-acetophenone-[4.5-diphenyl-oxazolyl-(2)]-hydrazone (IMET 98/69) on lethal mengo virus encephalitis.

作者信息

Veckenstedt A

出版信息

Acta Virol. 1978 Jan;22(1):52-9.

PMID:25008
Abstract

3-[Bis-(2-hydroxyethyl)-amino]-acetophenone-[4.5-diphenyl-oxazolyl-(2)]-hydrazone (IMET 98/69) was found to afford maximum "rates of protection" in intraperitoneally (i.p.) or intranasally (i.n.) induced Mengo virus encephalitis in mice when administered once daily at doses of 1 mmole/kg (456.5 mg/kg) subcutaneously (s.c.) or 4 mmoles/kg (1 826 mg/kg) perorally (p.o.). Three days of treatment were sufficient if started on the day before or at the time of virus inoculation. Initiation of treatment 6 hours after inoculation was no longer effective. In a remarkable number of brains from infected and treated mice no virus was detectable, while in the remaining brains the appearance of virus was strongly delayed, and its amount significantly reduced.

摘要

3-[双-(2-羟乙基)-氨基]-苯乙酮-[4,5-二苯基-恶唑基-(2)]-腙(IMET 98/69)被发现,当以1毫摩尔/千克(456.5毫克/千克)的剂量皮下注射或4毫摩尔/千克(1826毫克/千克)的剂量口服,每日给药一次时,对小鼠腹腔内或鼻内感染的门戈病毒脑炎能提供最大的“保护率”。如果在病毒接种前一天或接种时开始治疗,三天的治疗就足够了。接种后6小时开始治疗不再有效。在大量感染并接受治疗的小鼠大脑中检测不到病毒,而在其余大脑中,病毒的出现被强烈延迟,其数量显著减少。

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