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Authordc.contributor.authorOlea Azar, Claudio 
Authordc.contributor.authorRigol Olsen, Carolina es_CL
Authordc.contributor.authorOpazo, L. es_CL
Authordc.contributor.authorMorello Casté, Antonio es_CL
Authordc.contributor.authorMaya Arango, Juan es_CL
Authordc.contributor.authorRepetto Scaramelli, Yolanda es_CL
Authordc.contributor.authorAguirre, G. es_CL
Authordc.contributor.authorCerecetto, Hugo es_CL
Authordc.contributor.authorDi Maio, R. es_CL
Authordc.contributor.authorGonzález, M. es_CL
Authordc.contributor.authorPorcal, Williams es_CL
Admission datedc.date.accessioned2010-06-08T15:17:59Z
Available datedc.date.available2010-06-08T15:17:59Z
Publication datedc.date.issued2003-12
Cita de ítemdc.identifier.citationJOURNAL OF THE CHILEAN CHEMICAL SOCIETY 48 (4): 77-79en_US
Identifierdc.identifier.issn0717-9324
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/120975
Abstractdc.description.abstractThe Electron Spin Resonance (ESR) spectra of radicals obtained from two new potential antitrypanosomal drugs by Trypanosoma cruzi reduction were analyzed. DMPO Spin Trapping was used to investigate the possible formation of free radicals in the trypanosome microsomal system. The Nitro 2 (4-(n-butyl)-1-(5-nitrofurfurylidene)semicarbazide) analogue of Nifurtimox showed better antiparasitic activity than N-oxide 1 (4-(n-butyl)-1-[(7-bromo-N1-oxidebenzo[1,2-c]1,2,5-oxadiazole-5-yl)methylidene]semicarbazide). Only Nitro 2 could produce oxygen redox cycling in T. cruzi epimastigotes. The ESR signal intensities were consistent with the trapping of hydroxyl radical. These results are in agreement with the biological observation that Nitro 2 showed antichagasic activity by an oxidative stress mechanism.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherSOCIEDAD CHILENA DE QUIMICAen_US
Keywordsdc.subjectNitrofuran derivativesen_US
Títulodc.titleESR and spin trapping studies of two new potential antitrypanosomal drugsen_US
Document typedc.typeArtículo de revista


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