Pralidoxime Rescues Both Muscarinic and Nicotinic Systems
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Anesthesiology and Pain Medicine
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1. A powerful reactivator of alkylphosphate-inhibited acetylcholinesterase
2. Protective Drugs in Acute Large-Dose Exposure to Organophosphates: A Comparison of Metoclopramide and Tiapride with Pralidoxime in Rats
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1. Investigation of the Experimental Pharmacokinetics of the Bis-Chlorinated Bis-pyridinium Mono-aldoxime Cholinesterase Reactivator K-868 in Rats;The Open Medicinal Chemistry Journal;2021-12-23
2. Pharmacokinetics of a Mono-pyridinium-mono-aldoxime (K-347), a Potential Antidote in Organophosphate Poisoning;The Open Medicinal Chemistry Journal;2020-11-13
3. The history of cholinesterase reactivation: hydroxylamine and pyridinium aldoximes;PHARMAZIE;2012
4. Efficacy of two new asymmetric bispyridinium oximes (K-27 and K-48) in rats exposed to diisopropylfluorophosphate: comparison with pralidoxime, obidoxime, trimedoxime, methoxime, and HI-6;Toxicology Mechanisms and Methods;2009-05
5. Pyridinium Oxime Reactivators of Cholinesterase Inhibited by Diisopropyl- Fluorophosphate (DFP): Predictive Value of In-Vitro Testing for In-Vivo Efficacy;Mini-Reviews in Medicinal Chemistry;2008-11-01
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