Journal
MINI-REVIEWS IN MEDICINAL CHEMISTRY
Volume 6, Issue 3, Pages 269-277Publisher
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138955706776073510
Keywords
acetylcholinesterase; nerve agent; pesticide; antidote; reactivator; structural requirements
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Nerve agents (sarin, soman, cyclosarin, tabun and VX agent) and pesticides (paraoxon, chlorpyrifos, TEPP) represent extremely toxic group of organophosphorus compounds (OPCs). These compounds inhibit enzyme acetylcholinesterase (ACNE, EC 3.1.1.7) via its phosphorylation or phosphonylation at the serine hydroxy group in its active site. Afterwards, ACNE is not able to serve its physiological function and intoxicated organism is died due to overstimulation of cholinergic nervous system. The current standard treatment of poisoning with highly toxic OPCs usually consists of the combined administration of anticholinergic drugs (preferably atropine) and ACNE reactivators (called oximes). Anticholinergic drugs block effects of accumulated neurotransmitter acetylcholine at nicotinic and muscarinic receptor sites, while oximes reactivate ACNE inhibited by OPCs. Unfortunately, none from the currently used oximes is sufficiently effective against all known nerve agents and pesticides. Therefore, to find new oximes able to sufficiently reactivate inhibited ACNE (regardless of the type of OPCs) is still very important task for medicinal chemistry with the aim to improve the efficacy of antidotal treatment of the acute poisonings mentioned. In this paper, the relationship between chemical structure of ACNE reactivators and their ability to reactivate ACNE inhibited by several nerve agents and pesticides is summarized. It is shown that there are several structural fragments possibly involving in the structure of proposed ACNE reactivators. Finally, an attempt of a future course of new ACNE reactivators development is discussed.
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