Reactivators of organophosphate-inhibited cholinesterase

Fühner-Wieland's Sammlung von Vergiftungsfällen - Tập 49 - Trang 285-291 - 1982
Vjera Deljac1, Matej Maksimović2, Ljiljana Radović2, Dušanka Rakin2, Verica Markov2, Ivo Bregovec1, Zlatko Binenfeld1
1Laboratory of Organic Chemistry and Biochemistry, Faculty of Natural Sciences and Mathematics, University of Zagreb, Zagreb
2Medical Department, Military Technical Institute, Belgrade, Yugoslavia

Tóm tắt

Eleven isomeric phenylhydroxymethyl and cyclohexylhydroxymethyl derivatives of 1-(2-hydroxyiminomethyl-1-pyridinio)-3-(1-pyridinio)-2-oxapropane diiodide and 1-(4-hydroxyiminomethyl-1-pyridinio)-3-(1-pyridinio)-2-oxapropane diiodide were prepared and characterized by spectroscopic methods and pKa values. The inhibitory power (I50) of the investigated oximes was determined on purified bovine erythrocyte AChE and human erythrocyte AChE. Percentage of reactivation after 30 min was estimated after inhibition of human erythrocyte AChE by sarin, VX, and paraoxon. The in vitro protective index against inhibition by soman has been calculated using bovine erythrocyte AChE. Their I50 for human erythrocyte AChE varied in the range of 9–61 (10−4 mol · dm−3) and for purified bovine erythrocyte AChE in the range of 11–57 (10−5 mol · dm−3). With 2 × 10−5 mol · dm−3 of oximes the percent of reactivation was: 0–63% for paraoxon inhibited AChE, 12–73% for sarin inhibited AChE and 11–80% for VX inhibited AChE. With the exception of 1-(2-hydroxyiminomethyl-1-pyridinio)-3-(4-phenylhydroxymethyl-1-pyridinio)-2-oxapropane diiodide (6) the derivatives of 4-hydroxyiminomethylpyridine are by far better reactivators. None of the compounds could protect purified bovine erythrocyte AChE from inhibition by soman.

Tài liệu tham khảo

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