dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-12-03T13:11:28Z
dc.date.available2014-12-03T13:11:28Z
dc.date.created2014-12-03T13:11:28Z
dc.date.issued2013-10-01
dc.identifierToxicological And Environmental Chemistry. Abingdon: Taylor & Francis Ltd, v. 95, n. 9, p. 1506-1517, 2013.
dc.identifier0277-2248
dc.identifierhttp://hdl.handle.net/11449/113182
dc.identifier10.1080/02772248.2014.892748
dc.identifierWOS:000334906700006
dc.description.abstractIncubation of guanosine and Sudan III induces the formation of a stable adduct, which may be identified using a spectrophotometric technique and mass spectroscopy. The high nucleophilicity of the C-8 position and its proximity to N-7 makes the site susceptible to a nucleophilic attack, which explains the S(N)2 reaction detected between guanosine and Sudan III dye. In addition, direct interaction of Sudan III with calf thymus DNA was monitored using a simple spectrophotometric technique. The results presented indicate that a simple modification of the chemical structure of Sudan I (monoazo dye) to Sudan III (diazo dye) markedly alters reactivity towards nitrogenous DNA bases.
dc.languageeng
dc.publisherTaylor & Francis Ltd
dc.relationToxicological and Environmental Chemistry
dc.relation0.972
dc.relation0,313
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectSudan dye adducts
dc.subjecttoxicology of azo dyes
dc.subjectSudan III dye
dc.titleIdentification of Sudan III-(deoxy)-guanosine adducts formed in situ in a reaction with no catalyst
dc.typeArtículos de revistas


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