Suppr超能文献

引起迟发性神经毒性效应的有机磷酸酯:作用机制与构效关系研究

Organophosphorus esters causing delayed neurotoxic effects: mechanism of action and structure activity studies.

作者信息

Johnson M K

出版信息

Arch Toxicol. 1975 Dec 18;34(4):259-88. doi: 10.1007/BF00353848.

Abstract

Evidence is reviewed that the initial biochemical event leading to delayed neurotoxicity is phosphorylation of the active site of a specific enzyme called Neurotoxic Esterase. This is followed by a bondcleavage (? hydrolytic) leading to formation of a mono-substituted phosphoric acid residue on the protein. The mechanism by which some phosphinates protect hens against neurotoxic compounds is explained. Screening Assay. Assay of effects of compounds on Neurotoxic Esterase activity of hen brain in vitro and in vivo provides a quick biochemical screen to supplement the 3-week clinical test. This test provides an estimate of safety margin for compounds which give negative results in the clinical test and are currently used as pesticides, plasticisers, etc. Simplified assay procedures are being developed. Structure/Activity Studies. Data is now available for the biochemical and neurotoxic activity of many compounds. This provides a basis for structure/activity predictions; neurotoxicity data published since 1930 has been assessed in this light.

摘要

有证据表明,导致迟发性神经毒性的初始生化事件是一种名为神经毒性酯酶的特定酶的活性位点发生磷酸化。随后发生键断裂(?水解),导致蛋白质上形成单取代磷酸残基。解释了一些次膦酸酯保护母鸡免受神经毒性化合物影响的机制。筛选测定。化合物对母鸡大脑神经毒性酯酶活性的体外和体内测定提供了一种快速生化筛选方法,以补充为期3周的临床试验。该试验为在临床试验中得出阴性结果且目前用作农药、增塑剂等的化合物提供了安全边际估计。正在开发简化的测定程序。构效关系研究。现在已有许多化合物的生化和神经毒性活性数据。这为构效关系预测提供了基础;自1930年以来发表的神经毒性数据已据此进行评估。

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