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双吡咯烷基乙酰胺芴酮(MLU-B75)、双二丙基氨基乙酰胺芴酮(MLU-B76)与盐酸替洛隆在小鼠体内抗病毒特性的比较。

Comparison of antiviral properties in mice of bis-pyrrolidinoacetamido-fluorenone (MLU-B75), bis-dipropylaminoacetamido-fluorenone (MLU-B76), and tilorone hydrochloride.

作者信息

Veckenstedt A, Witkowski W, Hoffmann S

出版信息

Acta Virol. 1979 Mar;23(2):153-8.

PMID:39439
Abstract

Like tilorone . HCl, its analogues, bis-pyrrolidinoacetamido-fluorenone (MLU-B75), and bis-dipropylaminoacetamido-fluorenone (MLU-B76), significantly protected mice against intraperitoneal challenge with a lethal dose of Mengo virus when administered prophylactically in a single oral dose of 250 mg per kg body weight. At lower doses the antiviral activity of MLU-B75 and MLU-B76 decreased more rapidly than that of tilorone. HCl. At the dose of 250 mg per kg the degree of antiviral protection and the titre of interferon induced by tilorone. HCl correlated well, but there was no correlation between the extent of protection and the detected amount of virus inhibitor induced by MLU-B76. It remains to be determined whether the antiviral protection elicited by the analogues of tilorone is mediated by interferon.

摘要

与盐酸泰洛龙一样,其类似物双吡咯烷基乙酰胺芴酮(MLU-B75)和双二丙基氨基乙酰胺芴酮(MLU-B76),当以每千克体重250毫克的单次口服剂量预防性给药时,能显著保护小鼠免受致死剂量门戈病毒的腹腔攻击。在较低剂量下,MLU-B75和MLU-B76的抗病毒活性比盐酸泰洛龙下降得更快。在每千克250毫克的剂量下,盐酸泰洛龙诱导的抗病毒保护程度与干扰素滴度相关性良好,但MLU-B76诱导的保护程度与检测到的病毒抑制剂量之间没有相关性。泰洛龙类似物引发的抗病毒保护是否由干扰素介导还有待确定。

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