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3-(1-甲基-5-硝基-2-咪唑基亚甲基氨基)-2-恶唑烷酮对巴斯德氏菌的体外和体内活性

In vitro and in vivo activity of 3-(1-methyl 1-5-nitro-2-imidazolylmethylideneamino)-2-oxazolidinone against Pasteurella.

作者信息

Frost B M, Valiant M E, Dulaney E L

出版信息

Chemotherapy. 1976;22(5):324-30. doi: 10.1159/000221940.

Abstract

Furazolidone was more active than 3-(1-methyl)-5-nitro-2-imidazolyl-methylideneamino)-2-oxazolidinone (MABN) against a series of 34 isolates of Pasteurella and 11 of Yersinia (formerly designated Pasteurella). However, the nitroimidazole was superior to furazolidone by both subcutaneous and oral routes against a series of mouse infections incited by strains of Pasteurella. It also was superior to furazolidone and sulfaquinoxaline when administered in the diet against two Pasteurella strains in a fowl cholera model infection in chickens. The good in vitro activity of MABN plus its low toxicity suggest its further study as an agent for fowl cholera and the shipping fever complex of cattle.

摘要

对一系列34株多杀巴斯德氏菌和11株耶尔森氏菌(以前称为巴斯德氏菌)而言,呋喃唑酮比3-(1-甲基)-5-硝基-2-咪唑基亚甲基氨基)-2-恶唑烷酮(MABN)更具活性。然而,在一系列由多杀巴斯德氏菌菌株引发的小鼠感染中,该硝基咪唑通过皮下和口服途径均优于呋喃唑酮。在鸡霍乱模型感染中,当在饲料中给药时,它也优于呋喃唑酮和磺胺喹恶啉,用于对抗两种多杀巴斯德氏菌菌株。MABN良好的体外活性及其低毒性表明,它可作为治疗禽霍乱和牛运输热综合征的药物作进一步研究。

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