dc.creatorGoulart M.O.F.
dc.creatorDe Souza A.A.
dc.creatorSales E.M.
dc.creatorDe Abreu F.C.
dc.creatorDe Paula F.S.
dc.creatorAlmeida W.P.
dc.date2007
dc.date2015-06-30T18:53:10Z
dc.date2015-11-26T14:39:20Z
dc.date2015-06-30T18:53:10Z
dc.date2015-11-26T14:39:20Z
dc.date.accessioned2018-03-28T21:44:56Z
dc.date.available2018-03-28T21:44:56Z
dc.identifier9781604233803
dc.identifierEcs Transactions. , v. 3, n. 29, p. 137 - 146, 2007.
dc.identifier19385862
dc.identifier10.1149/1.2753298
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-44849118824&partnerID=40&md5=f99ccb55d308d23011d1b0bd5aa6500b
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/105248
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/105248
dc.identifier2-s2.0-44849118824
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1249953
dc.descriptionElectrochemical experiments (CV, DPV, SWV, CPE) with methyl 2-[p-nitrophenyl(hydroxy) methyl] acrylate (1) were performed in protic (EtOH + phosphate buffer 1:9, 0.1 mol L-1, pH 6.9 and EtOH + phosphate buffer: 1:9, 0.1 mol L1, pH 9.4) and aprotic (DMF + TBAP, 0.1 mol L-1) media. The reduction behaviours were typical of nitroaromatics, with an additional wave, in aprotic medium, related to the reduction of the olefin. Electrolysis, in protic media, furnished a reduced dimer. The incubation of 1 into a dsDNA biosensor revealed, that, after reduction of the nitroaromatic function, diagnostic oxidation peaks of the nucleobases were observed, indicative of interaction between them. GSH influenced the reduction behaviour of 1. Direct reduction of 1, in phosphate buffer, pH 9.38, to a stable nitroso/GSH adduct is facilitated. These electrochemical results help in the understanding of the anticancer activity of 1 that can be considered a hypoxia targeted bioreductive agent with a glutathione depleting function. copyright The Electrochemical Society.
dc.description3
dc.description29
dc.description137
dc.description146
dc.descriptionRauf, S., Gooding, J.J., Akhtar, K., Ghauri, M.A., Rahman, M., Anwar, M.A., Khalid, A.M., (2005) J. Pharm. Biomed. Anal, 37, p. 205
dc.descriptionRusso, A., Degraff, W., Friedman, N., Mitchell, J.B., (1986) Cancer Res, 46, p. 2845
dc.descriptionTew, K.D., (1994) Cancer Res, 54, p. 4313
dc.descriptionBerube, L.R., Farah, S., McClelland, R.A., Rauth, A.M., (1992) Int. J. Radiat. Oncol. Biol. Phys, 22, p. 817
dc.descriptionGriffith, O.W., Meister, A., (1979) J. Biol. Chem, 254, p. 7558
dc.descriptionWilliamson, J.M., Boettcher, B., Meister, A., (1982) Proc. Natl. Acad. Sci. USA, 79, p. 6246
dc.descriptionMcCarthy, T.J., Hayes, E.P., Schwartz, C.S., Witz, G., (1994) Fundam. Appl. Toxicol, 22, p. 543
dc.descriptionKohn, L.K., Pavam, C.H., Veronese, D., Coelho, F., De Carvalho, J.E., Almeida, W.P., (2006) Eur. J. Med. Chem, 41, p. 738
dc.descriptionDe Abreu, F.C., Ferraz, P.A.L., Goulart, M.O.F., (2002) J. Braz. Chem. Soc, 13, p. 19
dc.descriptionSquella, J.A., Bollo, S., Núñez-Vergara, L.J., (2005) Current Org. Chem, 9, p. 565
dc.descriptionJulião, M.D.D.S., Ferreira, E.I., Ferreira, N.G., Serrano, S.H.P., (2006) Electrochim. Acta, 51, p. 5080
dc.descriptionA. M. O. Brett, M.O.F.
dc.descriptionGoulart and F.C. de Abreu, Biosens. Bioelectron., 17, 913 (2002)Brett, A.M.O., Serrano, S.H.P.J., Piedade, A.P., (1999) Comprehensive Chemical Kinetics, 37, pp. 91-119. , R. G. Compton and H. G. Hancock, Editors, Elsevier: Amsterdam
dc.descriptionCoelho, F., Almeida, W.P., Mateus, C.R., Veronese, D., Lopes, E.C.S., Silvira, G.P.S., Rossi, R.C., Pavam, C.H., (2002) Tetrahedron, 58, p. 7437
dc.descriptionLund, H., Cathodic Reduction of Nitro and Related Compounds (2001) Organic Electrochemistry, p. 389. , 4th Ed, H. Lund and O. Hammerich, Editors, p, Marcel Dekker, New York
dc.descriptionMcClelland, R.A., (1990) Selective Activation of Drugs by Redox Processes, p. 125. , G.E. Adams, A. Breccia, E.M. Fielden and P. Wardman, Editors, p, Plenum Press, New York
dc.descriptionTocher, J.H., Edwards, D.I., (1995) Biochem. Pharmacol, 50, p. 1367
dc.languageen
dc.publisher
dc.relationECS Transactions
dc.rightsfechado
dc.sourceScopus
dc.titleElectrochemical Study Of Methyl 2-[p-nitrophenyi(hydroxy)methyl]acrylate, An Anticancer Drug, In The Presence Of Gsh And Dsdna
dc.typeActas de congresos


Este ítem pertenece a la siguiente institución