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Synthesis, in vitro screening and molecular docking of isoquinolinium-5-carbaldoximes as acetylcholinesterase and butyrylcholinesterase reactivators

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dc.rights.license CC BY eng
dc.contributor.author Maliňák, Dávid cze
dc.contributor.author Doležal, Rafael cze
dc.contributor.author Hepnarova, Vendula cze
dc.contributor.author Hozova, Miroslava cze
dc.contributor.author Andrýs, Rudolf cze
dc.contributor.author Bzonek, Petr cze
dc.contributor.author Račáková, Veronika cze
dc.contributor.author Korabecny, Jan cze
dc.contributor.author Gorecki, Lukas cze
dc.contributor.author Mezeiova, Eva cze
dc.contributor.author Psotka, Miroslav cze
dc.contributor.author Jun, Daniel cze
dc.contributor.author Kuča, Kamil cze
dc.contributor.author Musílek, Kamil cze
dc.date.accessioned 2025-12-05T08:40:15Z
dc.date.available 2025-12-05T08:40:15Z
dc.date.issued 2020 eng
dc.identifier.issn 1475-6366 eng
dc.identifier.uri http://hdl.handle.net/20.500.12603/966
dc.description.abstract The series of symmetrical and unsymmetrical isoquinolinium-5-carbaldoximes was designed and prepared for cholinesterase reactivation purposes. The novel compounds were evaluated for intrinsic acetylcholinesterase (AChE) or butyrylcholinesterase (BChE) inhibition, when the majority of novel compounds resulted with high inhibition of both enzymes and only weak inhibitors were selected for reactivation experiments on human AChE or BChE inhibited by sarin, VX, or paraoxon. The AChE reactivation for all used organophosphates was found negligible if compared to the reactivation ability of obidoxime. Importantly, two compounds were found to reactivate BChE inhibited by sarin or VX better to obidoxime at human attainable concentration. One compound resulted as better reactivator of NEMP (VX surrogate)-inhibited BChE than obidoxime. The in vitro results were further rationalized by molecular docking studies showing future directions on designing potent BChE reactivators. eng
dc.format p. 478-488 eng
dc.language.iso eng eng
dc.publisher Taylor & Francis eng
dc.relation.ispartof Journal of enzyme inhibition and medicinal chemistry, volume 35, issue: 1 eng
dc.subject Acetylcholinesterase eng
dc.subject butyrylcholinesterase eng
dc.subject organophosphate eng
dc.subject reactivator eng
dc.subject oxime eng
dc.subject Acetylcholinesterase cze
dc.subject butyrylcholinesterase cze
dc.subject organophosphate cze
dc.subject reactivator cze
dc.subject oxime cze
dc.title Synthesis, in vitro screening and molecular docking of isoquinolinium-5-carbaldoximes as acetylcholinesterase and butyrylcholinesterase reactivators eng
dc.title.alternative Synthesis, in vitro screening and molecular docking of isoquinolinium-5-carbaldoximes as acetylcholinesterase and butyrylcholinesterase reactivators cze
dc.type article eng
dc.identifier.obd 43876032 eng
dc.identifier.wos 000506063900001 eng
dc.identifier.doi 10.1080/14756366.2019.1710501 eng
dc.description.abstract-translated The series of symmetrical and unsymmetrical isoquinolinium-5-carbaldoximes was designed and prepared for cholinesterase reactivation purposes. The novel compounds were evaluated for intrinsic acetylcholinesterase (AChE) or butyrylcholinesterase (BChE) inhibition, when the majority of novel compounds resulted with high inhibition of both enzymes and only weak inhibitors were selected for reactivation experiments on human AChE or BChE inhibited by sarin, VX, or paraoxon. The AChE reactivation for all used organophosphates was found negligible if compared to the reactivation ability of obidoxime. Importantly, two compounds were found to reactivate BChE inhibited by sarin or VX better to obidoxime at human attainable concentration. One compound resulted as better reactivator of NEMP (VX surrogate)-inhibited BChE than obidoxime. The in vitro results were further rationalized by molecular docking studies showing future directions on designing potent BChE reactivators. cze
dc.publicationstatus postprint eng
dc.peerreviewed yes eng
dc.source.url https://www.tandfonline.com/doi/full/10.1080/14756366.2019.1710501 cze
dc.relation.publisherversion https://www.tandfonline.com/doi/full/10.1080/14756366.2019.1710501 eng
dc.rights.access Open Access eng


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