MMSL 1998, 67(S1):11-13

THE REACTIVATORS OF ISOPROPYLMETHYL-PHOSPHONYLATED ACETYLCHOLINESTERASE DERIVED FROM 2-HYDROXYIMINOMETHYLPYRIDINE

Jiří Patočka, Jiří Cabal, Jiří Bielavský, Josef Vachek
Purkyně Military Medical Academy, Hradec Králové

Four new 4-substituted pyridinium-2-aldoxime methoiodides were prepared and their physico-chemical properties were estimated, including their pKa values. Compounds were tested as reactivators of acetylcholinesterase inhibited by isopropyl-methylphosphonofluoridate in vitro. Their acute toxicities were estimated in mice after i.m. administration. Results show that these compounds are less toxic than 2—pyridinium-aldoxime methiodide (2-PAM) alone, but only one compound was better reactivator than 2-PAM.

Keywords: Acetylcholinesterase; Organophosphates; Inhibition; Pyridinium-Aldoxlmes; Reactivators

Published: September 1, 1998  Show citation

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Patočka, J., Cabal, J., Bielavský, J., & Vachek, J. (1998). THE REACTIVATORS OF ISOPROPYLMETHYL-PHOSPHONYLATED ACETYLCHOLINESTERASE DERIVED FROM 2-HYDROXYIMINOMETHYLPYRIDINE. Vojenské Zdravotnické Listy67(Suppl.1), 11-13
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