Suppr超能文献

[非特异性大鼠肝微粒体氧化酶在N1-呋喃基嘧啶破坏中的作用]

[Participation of non-specific rat liver microsome oxidases in destruction of Nl-furanidylpyrimidines].

作者信息

Meĭren D V, Urbanovich E L, Sniedze T N, Khagi Kh B, Gilev A P

出版信息

Biull Eksp Biol Med. 1977 Feb;83(2):162-4.

PMID:15682
Abstract

N1-(3'-Butyrolactono)-5-fluorouracil, N1-(2'-furanidyl) 5-trifluoromethyluracil, N1-(2'-furanidyl)-5-fluoracil are split in the rat organism with the formation of free 5-fluorouracil. The destruction of the C--N bonds in the molecule of the N1-(2'-furanidyl)-5-fluoracil takes place in the liver microsomes. This process is strengthened by NADPH and weakened by SKF-525A. All the three furanidylpyrimidines studied induced differential spectra of type I in the suspension of the liver microsomes. This fact testifies to the interaction of these substances with the cytochrome P-450.

摘要

N1-(3'-丁内酯基)-5-氟尿嘧啶、N1-(2'-呋喃基)-5-三氟甲基尿嘧啶、N1-(2'-呋喃基)-5-氟尿嘧啶在大鼠体内分解,生成游离的5-氟尿嘧啶。N1-(2'-呋喃基)-5-氟尿嘧啶分子中的C-N键在肝脏微粒体中发生断裂。此过程因NADPH而增强,因SKF-525A而减弱。所研究的三种呋喃基嘧啶在肝脏微粒体悬液中均诱导出I型差异光谱。这一事实证明这些物质与细胞色素P-450发生了相互作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验