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Synthesis, antifungal activity of caffeic acid derivative esters, and their synergism with fluconazole and nystatin against Candida spp.

dc.contributor.authorSardi, Janaína de Cássia Orlandi [UNESP]
dc.contributor.authorGullo, Fernanda Patrícia [UNESP]
dc.contributor.authorFreires, Irlan Almeida
dc.contributor.authorPitangui, Nayla de Souza [UNESP]
dc.contributor.authorSegalla, Maicon Petrônio [UNESP]
dc.contributor.authorFusco-Almeida, Ana Marisa [UNESP]
dc.contributor.authorRosalen, Pedro Luiz
dc.contributor.authorRegasini, Luís Octávio [UNESP]
dc.contributor.authorMendes-Giannini, Maria José Soares [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionLetters and Exact Sciences
dc.date.accessioned2018-12-11T17:07:27Z
dc.date.available2018-12-11T17:07:27Z
dc.date.issued2016-12-01
dc.description.abstractWe tested the antifungal potential of caffeic acid and 8 of its derivative esters against Candidaalbicans ATCC 90028 and 9 clinical isolatesand carried out a synergism assay with fluconazole and nystatin. Propyl caffeate (C3) showed the best antifungal activity against the tested strains. When in combination, C3 markedly reduced the MIC of fluconazole and nystatin with synergistic effect up to 64-fold. Finally, C3 showed a high IC50 value and selective indexagainst oral keratinocytes, demonstrating low toxicity against this cell type and selectivity for yeast cells. Further research should confirm its antifungal potential for development of combined therapy to treat C. albicans infections.en
dc.description.affiliationDepartment of Clinical Analysis Laboratory of Clinical Mycology Faculty of Pharmaceutical Sciences UNESP–Univ Estadual Paulista
dc.description.affiliationDepartment of Biochemistry and Chemical Technology Institute of Chemistry UNESP–Univ Estadual Paulista
dc.description.affiliationDepartment of Physiological Sciences Piracicaba Dental School University of Campinas
dc.description.affiliationDepartment of Chemistry and Environmental Sciences Institute of Biosciences Letters and Exact Sciences
dc.description.affiliationUnespDepartment of Clinical Analysis Laboratory of Clinical Mycology Faculty of Pharmaceutical Sciences UNESP–Univ Estadual Paulista
dc.description.affiliationUnespDepartment of Biochemistry and Chemical Technology Institute of Chemistry UNESP–Univ Estadual Paulista
dc.format.extent387-391
dc.identifierhttp://dx.doi.org/10.1016/j.diagmicrobio.2016.08.002
dc.identifier.citationDiagnostic Microbiology and Infectious Disease, v. 86, n. 4, p. 387-391, 2016.
dc.identifier.doi10.1016/j.diagmicrobio.2016.08.002
dc.identifier.file2-s2.0-84994234378.pdf
dc.identifier.issn1879-0070
dc.identifier.issn0732-8893
dc.identifier.lattes0992736452764550
dc.identifier.scopus2-s2.0-84994234378
dc.identifier.urihttp://hdl.handle.net/11449/173724
dc.language.isoeng
dc.relation.ispartofDiagnostic Microbiology and Infectious Disease
dc.relation.ispartofsjr1,157
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectAntifungal
dc.subjectCaffeic acid
dc.subjectCandida albicans
dc.subjectSynergism
dc.titleSynthesis, antifungal activity of caffeic acid derivative esters, and their synergism with fluconazole and nystatin against Candida spp.en
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.author.lattes0992736452764550[8]
unesp.author.lattes3716273524139678[6]
unesp.author.orcid0000-0002-3705-0971[8]
unesp.author.orcid0000-0002-2115-8988[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentAnálises Clínicas - FCFpt
unesp.departmentBioquímica e Tecnologia - IQpt

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