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dc.contributor.authorBrango Vanegas, José-
dc.contributor.authorMartinho, Luan Alves-
dc.contributor.authorBessa, Lucinda J.-
dc.contributor.authorVasconcelos, Andreanne Gomes-
dc.contributor.authorPlácido, Alexandra-
dc.contributor.authorPereira, Alex Leite-
dc.contributor.authorLeite, José Roberto de Souza de Almeida-
dc.contributor.authorMachado, Angelo Henrique de Lira-
dc.date.accessioned2020-01-30T12:22:32Z-
dc.date.available2020-01-30T12:22:32Z-
dc.date.issued2019-10-
dc.identifier.citationBRANGO-VANEGAS, José et al. Synthesis of novel sulfide-based cyclic peptidomimetic analogues to solonamides. Beilstein Journal of Organic Chemistry, v. 15, 2544-2551, out. 2019. DOI: https://doi.org/10.3762%2Fbjoc.15.247. Disponível em: https://www.beilstein-journals.org/bjoc/articles/15/247. Acesso em: 30 jan. 2020.pt_BR
dc.identifier.urihttps://repositorio.unb.br/handle/10482/36752-
dc.language.isoInglêspt_BR
dc.rightsAcesso Abertopt_BR
dc.titleSynthesis of novel sulfide-based cyclic peptidomimetic analogues to solonamidespt_BR
dc.typeArtigopt_BR
dc.subject.keywordAgentes antiviraispt_BR
dc.subject.keywordBactériaspt_BR
dc.subject.keywordPeptídeospt_BR
dc.rights.licenseThis is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited.pt_BR
dc.identifier.doihttps://doi.org/10.3762%2Fbjoc.15.247pt_BR
dc.description.abstract1Eight new sulfide-based cyclic peptidomimetic analogues of solonamides A and B have been synthesized via solid-phase peptide synthesis and SN2’ reaction on a Morita–Baylis–Hillman (MBH) residue introduced at the N-terminal of a tetrapeptide. This last step takes advantage of the electrophilic feature of the MBH residue and represents a new cyclization strategy occurring. The analogues were prepared in moderate overall yields and did not show toxic effects on Staphylococcus aureus growth and were not toxic to human fibroblasts. Two of them inhibited the hemolytic activity of S. aureus, suggesting an interfering action in the bacterial quorum sensing similar to the one already reported for solonamides.pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0003-4070-9770pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0001-6658-5847pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0001-8339-1964pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0003-2706-7777pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0002-0346-7146pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0002-1096-3236pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0003-4284-9929pt_BR
dc.description.unidadeInstituto de Química (IQ)pt_BR
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