1. Design, synthesis and evaluation of new α-nucleophiles for the hydrolysis of organophosphorus nerve agents: application to the reactivation of phosphorylated acetylcholinesterase
- Author
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Saint-André, Géraldine, Kliachyna, Maria, Kodepelly, Sanjeevarao, Louise-Leriche, Ludivine, Gillon, Emilie, Renard, Pierre-Yves, Nachon, Florian, Baati, Rachid, and Wagner, Alain
- Subjects
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ORGANIC synthesis , *NUCLEOPHILIC reactions , *HYDROLYSIS , *ORGANOPHOSPHORUS compounds , *NERVE gases , *PHOSPHORYLATION , *ACETYLCHOLINESTERASE , *ENZYME activation , *HYDROXYL group - Abstract
Abstract: A series of new α-nucleophiles including oximes and amidoximes have been synthesized, and their ability to efficiently and selectively cleave the P–S bond of organophosphorus nerve agents has been evaluated. The relationship between the chemical structure of the α-nucleophiles and their reactivity towards PhX hydrolysis is reported. A significant effect induced by an ortho-hydroxyl group of aryl- and pyridyl-oximes, amidoximes on their organo-phosphono-thioase reactivity was discovered. The evaluation of the initial rates of PhX hydrolysis reaction in the presence of α-nucleophiles allowed the discovery of new uncharged molecules with increased reactivity compared to positively charged 2-pralidoxime used as antidote. The mechanism of their action was studied in details by kinetic analysis, HPLC and LC–MS methods. The most promising structures were then considered as potent in vitro reactivators of phosphylated acetylcholinesterase (AChE), which was confirmed by the preliminary results of AChE reactivation initially inhibited by VX. [Copyright &y& Elsevier]
- Published
- 2011
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