Reactivation of organophosphate-inhibited serum butyrylcholinesterase by novel substituted phenoxyalkyl pyridinium oximes and traditional oximes
Author:
Funder
National Institute of Health
Publisher
Elsevier BV
Subject
Toxicology
Reference35 articles.
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3. Estimation of the upper limit of human butyrylcholinesterase dose required for protection against organophosphates toxicity: a mathematically based toxicokinetic model;Ashani;Toxicol. Sci.,2004
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5. Suitability of human butyrylcholinesterase as a therapeutic marker and pseudo catalytic scavenger in organophosphate poisoning: a kinetic analysis;Aurbek;Toxicology,2009
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Reactivators of butyrylcholinesterase inhibited by organophosphorus compounds;Bioorganic Chemistry;2024-09
2. Reactivation by novel pyridinium oximes of rat serum and skeletal muscle acetylcholinesterase inhibited by organophosphates;Journal of Biochemical and Molecular Toxicology;2024-07
3. Model acetylcholinesterase‐Fc fusion glycoprotein biotechnology system for the manufacture of an organophosphorus toxicant bioscavenging countermeasure;Bioengineering & Translational Medicine;2024-04-25
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