engleski

In Vitro Evaluation of Uncharged Thienostilbene Oximes as Reactivatiors of Organophosphate- inhibited Cholinesterases

The inhibition of AChE and BChE by organophosphates (OPs) as nerve agents and pesticides compromises normal cholinergic nerve signal transduction in the peripheral and central nervous systems (CNS) leading to cholinergic crisis. The treatment comprises an antimuscarinic drug and an oxime reactivator of the inhibited enzyme. Oximes in use have quaternary nitrogens, and therefore poorly cross the brain–blood barrier. In this work, we synthesized novel uncharged thienostilbene oximes by sequence of three reactions in very high yields. The expected targeted products were pure cis- and trans-isomers of syn- and anti-oximes containing different substituents bound in the para- position of the benzene ring.1 Eight trans, anti- and trans, syn-isomers of oximes were tested as reactivators of nerve-agent- inhibited AChE and BChE. Four derivatives reactivated cyclosarin- inhibited BChE up to 70% in two hours of reactivation, and docking studies confirmed their productive interactions with the active site of cyclosarin- inhibited BChE. Based on the moderate binding affinity of both AChE and BChE for all selected oximes, these compounds present a new class of oximes with the potential for further development of CNS- active therapeutics in OP poisoning. This is the first study to show the potential of thienostilbene oximes as therapeutics in OP poisoning, and it seems that further design of the compounds e.g., with amide, OH, mono- and dimethylamino groups, or triazole ring, could provide a new platform for further antidote and scavenger development for exposure to organophosphates.

AChE ; BChE ; reactivation ; heterostilbenes ; spectroscopy ; docking

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