Molecules (Dec 2009)

Novel Bisquaternary Oximes—Reactivation of Acetylcholinesterase and Butyrylcholinesterase Inhibited by Paraoxon

  • Daniel Jun,
  • Jana Zdarova Karasova,
  • Miroslav Pohanka,
  • Martina Hrabinova,
  • Kamil Musilek,
  • Martin Paar,
  • Vladimir Cirkva,
  • Jiri Palecek,
  • Kamil Kuca,
  • Lucie Musilova

DOI
https://doi.org/10.3390/molecules14124915
Journal volume & issue
Vol. 14, no. 12
pp. 4915 – 4921

Abstract

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Four novel bisquaternary aldoxime cholinesterase reactivators differing in their chemical structure were prepared. Afterwards, their biological activity was evaluated for their ability to reactivate acetylcholinesterase (AChE; EC 3.1.1.7) and butyrylcholinesterase (BuChE; EC 3.1.1.8) inhibited by paraoxon. Their reactivation activity was compared with standard reactivators—pralidoxime, obidoxime and HI-6—which are clinically used at present. As it resulted, none of the prepared compounds surpassed obidoxime, which is considered to be the most potent compound if used for reactivation of AChE inhibited by paraoxon. In case of BuChE reactivation, two compounds (K053 and K068) achieved similar results as obidoxime.

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