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dc.contributor.authorMozziconacci, Olivier
dc.contributor.authorWilliams, Todd D.
dc.contributor.authorSchöneich, Christian
dc.date.accessioned2017-05-08T16:16:28Z
dc.date.available2017-05-08T16:16:28Z
dc.date.issued2012-09-17
dc.identifier.citationMozziconacci, O., Williams, T. D., & Schöneich, C. (2012). Intramolecular hydrogen transfer reactions of thiyl radicals from glutathione: formation of carbon-centered radical at Glu, Cys and Gly. Chemical Research in Toxicology, 25(9), 1842–1861. http://doi.org/10.1021/tx3000494en_US
dc.identifier.urihttp://hdl.handle.net/1808/24001
dc.descriptionThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Chemical Research in Toxicology, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://pubs.acs.org/doi/abs/10.1021/tx3000494en_US
dc.description.abstractGlutathione thiyl radicals (GS•) were generated in H2O and D2O by either exposure of GSH to AAPH#, photoirradiation of GSH in the presence of acetone, or photoirradiation of GSSG. Detailed interpretation of the fragmentation pathways of deuterated GSH and GSH-derivatives during mass spectrometry analysis allowed us to demonstrate that reversible intramolecular H-atom transfer reactions between GS• and C-H bonds at Cys[αC], Cys[βC], and Gly[αC] are possible.en_US
dc.publisherACSen_US
dc.rights© 2012 American Chemical Societyen_US
dc.subjectGlutathioneen_US
dc.subjectThiyl radicalsen_US
dc.subjectC-centered radicalen_US
dc.subjectHydrogen transferen_US
dc.subjectMass spectrometryen_US
dc.titleIntramolecular hydrogen transfer reactions of thiyl radicals from glutathione: formation of carbon-centered radical at Glu, Cys and Glyen_US
dc.typeArticleen_US
kusw.kuauthorMozziconacci, Olivier
kusw.kuauthorSchöneich, Christian
kusw.kuauthorWilliams, Todd D.
kusw.kudepartmentPharmaceutical Chemistryen_US
kusw.kudepartmentLaboratory of Mass Spectrometryen_US
dc.identifier.doi10.1021/tx3000494en_US
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC3736831en_US
dc.rights.accessrightsopenAccess


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