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Activity of gallic acid and its ester derivatives in Caenorhabditis elegans and zebrafish (Danio rerio) models

dc.contributor.authorSingulani, Junya De Lacorte [UNESP]
dc.contributor.authorScorzoni, Liliana [UNESP]
dc.contributor.authorGomes, Paulo César [UNESP]
dc.contributor.authorNazaré, Ana Carolina [UNESP]
dc.contributor.authorPolaquini, Carlos Roberto [UNESP]
dc.contributor.authorRegasini, Luis Octávio [UNESP]
dc.contributor.authorFusco-Almeida, Ana Marisa [UNESP]
dc.contributor.authorMendes-Giannini, Maria José Soares [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:16:09Z
dc.date.available2018-12-11T17:16:09Z
dc.date.issued2017-10-01
dc.description.abstractAim: Gallic acid and its ester derivatives have shown antifungal activity in vitro. This study was performed to investigate their activity against Candida albicans and their toxicity in the animal models Caenorhabditis elegans and zebrafish embryos. Results: The compounds protected worms from C. albicans infection. The dodecyl gallate was the most effective. In zebrafish embryo, gallic acid and dodecyl gallate were the least toxic. Conclusion: Gallic acid and its ester derivatives have potential for in vivo use against C. albicans infection. The antifungal effects and toxicity of gallate esters in these alternative animal models were dependent on carbon chain length.en
dc.description.affiliationDepartment of Clinical Analysis School of Pharmaceutical Sciences São Paulo State University-UNESP
dc.description.affiliationDepartment of Chemistry and Environmental Sciences Institute of Biosciences Humanities and Exact Sciences São Paulo State University-UNESP
dc.description.affiliationUnespDepartment of Clinical Analysis School of Pharmaceutical Sciences São Paulo State University-UNESP
dc.description.affiliationUnespDepartment of Chemistry and Environmental Sciences Institute of Biosciences Humanities and Exact Sciences São Paulo State University-UNESP
dc.format.extent1863-1872
dc.identifierhttp://dx.doi.org/10.4155/fmc-2017-0096
dc.identifier.citationFuture Medicinal Chemistry, v. 9, n. 16, p. 1863-1872, 2017.
dc.identifier.doi10.4155/fmc-2017-0096
dc.identifier.issn1756-8927
dc.identifier.issn1756-8919
dc.identifier.lattes3637285622123132
dc.identifier.lattes0992736452764550
dc.identifier.orcid0000-0003-2440-8097
dc.identifier.scopus2-s2.0-85034666874
dc.identifier.urihttp://hdl.handle.net/11449/175523
dc.language.isoeng
dc.relation.ispartofFuture Medicinal Chemistry
dc.relation.ispartofsjr1,111
dc.relation.ispartofsjr1,111
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectalternative animal models
dc.subjectantifungal development
dc.subjectgallates
dc.subjectgallic acid
dc.subjectinfection
dc.titleActivity of gallic acid and its ester derivatives in Caenorhabditis elegans and zebrafish (Danio rerio) modelsen
dc.typeArtigo
unesp.author.lattes3637285622123132[3]
unesp.author.lattes0992736452764550
unesp.author.lattes3716273524139678[7]
unesp.author.orcid0000-0003-2440-8097[3]
unesp.author.orcid0000-0002-2115-8988[7]
unesp.departmentAnálises Clínicas - FCFpt

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