Universality of Oxime K203 for Reactivation of Nerve Agent-Inhibited AChE

Med Chem. 2015;11(7):683-6. doi: 10.2174/1573406411666150407154204.

Abstract

Oxime K203 seems to be the most promising oxime in case of reactivation of tabun-inhibited acetylcholinesterase (AChE). Although it was originally developed for treatment of tabun intoxications, it is able to reactivate cholinesterases inhibited by other nerve agents. This study is aimed at the evaluation of its potency in vitro against other nerve agents. For this purpose, sarin, tabun, cyclosarin, soman, VX, Russian VX and DFP were selected as members of the nerve agent family to check its universality. At high concentrations (10(-3) M), oxime K203 reached promising reactivation activity. At low concentrations, relevant for human use (10(-5) M), promising reactivation potency was obtained only with tabun. In conclusion, oxime K203 reactivates other nerve agents-inhibited cholinesterases, however its broad-spectrum reactivation is limited at high, for human not attainable, concentrations only.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / metabolism*
  • Animals
  • Cholinesterase Inhibitors / pharmacology*
  • Cholinesterase Reactivators / pharmacology*
  • Humans
  • Nerve Agents / pharmacology*
  • Oximes / pharmacology*
  • Pyridinium Compounds / pharmacology*
  • Rats

Substances

  • 1-(4-carbamoylpyridinium)-4-(4-hydroxyiminomethylpyridinium)but-2-ene
  • Cholinesterase Inhibitors
  • Cholinesterase Reactivators
  • Nerve Agents
  • Oximes
  • Pyridinium Compounds
  • Acetylcholinesterase