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Letters in Drug Design & Discovery


ISSN (Print): 1570-1808
ISSN (Online): 1875-628X

SAR Study on Reactivators of Ethyl-Paraoxon Inhibited Acetylcholinesterase

Author(s): Ondrej Holas, Kamil Musilek, Anna Horova, Veronika Opletalova and Kamil Kuca

Volume 9, Issue 6, 2012

Page: [587 - 594] Pages: 8

DOI: 10.2174/157018012800673083

Price: $65


The current treatment of organophosphorus compounds induced intoxication consists of combined administration of anticholinergic drug, oxime reactivator and anticonvulsant. Oxime reactivators are causal treatment of organophosphorus intoxication and they are able to cleave OP moiety from the molecule of inhibited acetylcholinesterase. Unfortunately, none of the currently used oximes is sufficiently effective against all nerve agents and pesticides. Thus, finding of new potent acetylcholinesterase reactivators is necessary.

In this study, the reactivation efficacy of three series of novel bisquaternary reactivators with prop-1,3-diyl, but-1,4-diyl and but-2-ene-1,4-diyl linker against paraoxon inhibited acetylcholinesterase in vitro is presented. The obtained results were compared to the commercially used reactivators (pralidoxime, trimedoxime, obidoxime, methoxime, asoxime). Some newly prepared compounds showed promising ability of paraoxon in vitro reactivation, even in human attainable plasma concentrations. The structure-activity relationship for reactivators of paraoxon induced inhibition was determined.

Keywords: Acetylcholinesterase, Organophosphate, Paraoxon, Reactivator, Oxime, SAR

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