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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/70908
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dc.contributor.authorBelén Tarallo, M.-
dc.contributor.authorCosta-Filho, A. J.-
dc.contributor.authorVieira, Ernanni D.-
dc.contributor.authorMonge, Antonio-
dc.contributor.authorLeite, Clarice Q.-
dc.contributor.authorPavan, Fernando Rogério-
dc.contributor.authorBorthagaray, Graciela-
dc.contributor.authorGambino, Dinorah-
dc.contributor.authorTorre, María H.-
dc.date.accessioned2014-05-27T11:23:51Z-
dc.date.accessioned2016-10-25T18:26:48Z-
dc.date.available2014-05-27T11:23:51Z-
dc.date.available2016-10-25T18:26:48Z-
dc.date.issued2009-01-01-
dc.identifierhttp://www.aqa.org.ar/pdf9701/9701art8.pdf-
dc.identifier.citationJournal of the Argentine Chemical Society, v. 97, n. 1, p. 80-89, 2009.-
dc.identifier.issn0365-0375-
dc.identifier.urihttp://hdl.handle.net/11449/70908-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/70908-
dc.description.abstractThree new mixed-chelate copper complexes with 3-aminoquinoxaline-2-carbonitrile N 1,N 4-dioxide derivatives and alanine as ligands were synthesized in solid state. The spectroscopic characterization (FTIR, EPR, UV-Vis) showed that copper coordinated through the amine and the N-oxide groups of the quinoxaline derivatives and the amine and carboxylate moieties from alanine forming a dimeric species. The tree complexes showed in vitro activity against M. tuberculosis H 37Rv (ATCC 27294) similar to that of ethambutol while they are inactive against E. coli and S. aureus.en
dc.format.extent80-89-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAntimycobacterial agents-
dc.subjectCopper complexes-
dc.subjectQuinoxaline derivatives-
dc.titleResearch of new mixed-chelate copper complexes with quinoxaline N 1,N 4,-dioxide derivatives and alanine as ligands, potential antimycobacterial agentsen
dc.typeoutro-
dc.contributor.institutionCátedra de Química Inorgánica-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidad de Navarra-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidad de la República, Gral-
dc.description.affiliationCátedra de Química Inorgánica, Gral Flores 2124, C. C. 1157, 11800 Montevideo-
dc.description.affiliationInstituto de Física de São Carlos Universidade de São Paulo, C.P. 369, 13560, São Carlos-
dc.description.affiliationCIFA Universidad de Navarra, Pamplona, España-
dc.description.affiliationFaculdade de Ciencias Farmacêuticas Unesp, C.P. 582, 14801-902-Araquara(SP)-
dc.description.affiliationCátedra de Microbiología Facultad de Química Universidad de la República, Gral, Flores 2124, C. C. 1157, 11800 Montevideo-
dc.description.affiliationUnespFaculdade de Ciencias Farmacêuticas Unesp, C.P. 582, 14801-902-Araquara(SP)-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of the Argentine Chemical Society-
dc.identifier.scopus2-s2.0-79959608363-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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