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新型大环内酯类抗生素醋酸麦迪霉素(美欧卡霉素)的毒理学研究。第四部分-4。美欧卡霉素代谢物的毒性:Mb2对小鼠的急性毒性。

Toxicological studies on a new macrolide antibiotic, midecamycin acetate (miocamycin). Part IV-4. Toxicity of metabolites of miocamycin: acute toxicity of Mb2 in mice.

作者信息

Yokota M, Takeda U, Odaki M, Sasaki H, Kawaoto H, Itoh T, Koeda T

出版信息

Jpn J Antibiot. 1984 Aug;37(8):1507-9.

PMID:6334174
Abstract

Miocamycin (MOM) is a derivative of midecamycin and is metabolized into 4 main metabolites. At previous study, LD0 values of Mb1 were estimated more than 5,000 mg/kg in male and female mice. The object of this study was to evaluate acute toxicity in male and female mice after single oral administration of Mb2, a metabolite of MOM, at a dose level of 5,000 mg/kg as the maximum physically applicable dose. It is concluded that LD0 values of Mb2 were estimated more than 5,000 mg/kg.

摘要

米卡霉素(MOM)是麦迪霉素的衍生物,可代谢为4种主要代谢物。在先前的研究中,Mb1对雄性和雌性小鼠的半数致死量(LD0)估计超过5000mg/kg。本研究的目的是评估在最大实际可行剂量5000mg/kg下,单次口服给予MOM的代谢物Mb2后,雄性和雌性小鼠的急性毒性。得出的结论是,Mb2的LD0值估计超过5000mg/kg。

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