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dc.contributor.advisorCallam, Christopher
dc.contributor.advisorYoder, Ryan
dc.contributor.advisorHadad, Christopher
dc.creatorFitzpatrick, Keegan
dc.date.accessioned2013-12-06T20:53:08Z
dc.date.available2013-12-06T20:53:08Z
dc.date.issued2013-12
dc.identifier.urihttp://hdl.handle.net/1811/58453
dc.description.abstractAcetylcholinesterase (AChE) is an essential enzyme in the human body, which hydrolyzes the neurotransmitter acetylcholine into choline and acetate at neurosynaptic junctions. Organophosphorus (OP) nerve agents such as Sarin, Soman, and Tabun are covalent inhibitors of AChE. Following exposure to OPs, AChE is inhibited and undergoes a subsequent irreversible aging process in which the OP-AChE adduct is de-alkylated, resulting in the accumulation of excess acetylcholine in the central nervous system. Current oxime-based pharmaceuticals can only be used to treat the inhibited AChE and are ineffective on the aged AChE. Our research focuses on re-activation of the aged AChE. Quinone methides (QM) have been shown to react with phosphates to form an O–C bond, and such structures may potentially reverse the damage done to the active site on aged AChE through a kinetically favored alkylation of the phosphylated serine residue in aged AChE. Computational methods were used to analyze the potential reaction pathways and docking poses in AChE of pyridine and pyridinium derived quinone methide precursors (QMPs). A model phosphonate group was created and used to study the SN1 and SN2 reaction pathways of the QMP via our computational protocol. The SN1 pathway was determined to be the most energetically favorable mechanism. Snapshots of an aged AChE were used for our docking calculations where the QMPs were allowed to interact with the enzyme active site. Based on docking studies, the most promising therapeutic QMPs are pyridinium complexes with a methylated nitrogen and the alkyl chain at a meta position relative to the oxygen substituent. Studies of molecular dynamic simulations are in progress.en_US
dc.description.sponsorshipThe Ohio State University Department of Chemistryen_US
dc.language.isoen_USen_US
dc.publisherThe Ohio State Universityen_US
dc.relation.ispartofseriesThe Ohio State University. Department of Chemistry Undergraduate Research Theses; 2013en_US
dc.subjectChemistryen_US
dc.subjectOrganic chemistryen_US
dc.subjectComputational chemistryen_US
dc.subjectEnzyme inhibitionen_US
dc.subjectQuinone methidesen_US
dc.titleComputational Insights into the Alkylation Reactions of Pyrdine and Pyridinium Quinone Methide Precursors: Studies Towards the Realkylation of Aged Acetylcholinesteraseen_US
dc.typeThesisen_US
dc.description.embargoNo embargoen_US
dc.rights.ccAttribution 3.0 United Statesen_US
dc.rights.ccurihttp://creativecommons.org/licenses/by/3.0/us/en_US
dc.description.academicmajorAcademic Major: Chemistryen_US


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States