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dc.creatorGiacoppo, Juliana de O. S.-
dc.creatorLima, Willian E. A. de-
dc.creatorKuča, Kamil-
dc.creatorCunha, Elaine F. F. da-
dc.creatorFrança, Tanos C. C.-
dc.creatorRamalho, Teodorico de C.-
dc.date.accessioned2020-05-24T22:50:56Z-
dc.date.available2020-05-24T22:50:56Z-
dc.date.issued2014-
dc.identifier.citationGIACOPPO, J. de O. S. et al. Chemical warfare: perspectives on reactivating the enzyme acetylcholinesterase inhibited by organophosphates. Military Medical Science Letters, [S.l.], v. 83, n. 4, p. 165-177, 2014. DOI: 10.31482/mmsl.2014.027.pt_BR
dc.identifier.urihttps://www.mmsl.cz/artkey/mms-201404-0004_chemical-warfare-perspectives-on-reactivating-the-enzyme-acetylcholinesterase-inhibited-by-organophosphates.phppt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/41185-
dc.description.abstractIt is known that nerve agents are potent inhibitors of acetylcholinesterase (AChE), the enzyme responsible for the hydrolysis of the neurotransmitter acetylcholine and, thus, transmission of nerve impulses. The process of AChE inhibition by nerve agents can be reversed by a nucleophile able to dephosphorylate the enzyme. In this sense, oximes exhibit this characteristic and are able to remove the neurotoxic and reactivate AChE. Here, we review experimental and theoretical results involving docking and quantum mechanical-molecular mechanics hybrid methods (QM/MM), using Molegro® and Spartan® softwares to analyze the interaction of different nerve agents and oximes with AChE and to evaluate kinetic constants of reactivation.pt_BR
dc.languageen_USpt_BR
dc.publisherUniversity of Defence, Faculty of Military Health Sciencespt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceMilitary Medical Science Letters (MMSL)pt_BR
dc.subjectChemical warfarept_BR
dc.subjectOrganophosphatespt_BR
dc.subjectOximespt_BR
dc.subjectDockingpt_BR
dc.subjectQM/MMpt_BR
dc.subjectQuantum mechanics/Molecular mechanics (QM/MM)pt_BR
dc.titleChemical warfare: perspectives on reactivating the enzyme acetylcholinesterase inhibited by organophosphatespt_BR
dc.typeArtigopt_BR
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