Study of a selected series of 3- and 4-Arylcoumarins as antifungal agents against Dermatophytic Fungi: T. rubrum and T. mentagrophytes

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Orgánicagl
dc.contributor.authorLópez Cisneros, Carmen Lucía
dc.contributor.authorCazar Ramírez, María Elena
dc.contributor.authorBailón Moscoso, Natalia
dc.contributor.authorGuardado Yordi, Estela
dc.contributor.authorBorges, Fernanda
dc.contributor.authorUriarte Villares, Eugenio
dc.contributor.authorMatos, Maria João
dc.date.accessioned2022-08-12T10:21:23Z
dc.date.available2022-08-12T10:21:23Z
dc.date.issued2021
dc.description.abstractThe main etiological agents in dermatophytosis of human skin and nails are Trichophyton, in particular Trichophyton rubrum (T. rubrum) and Trichophyton mentagrophytes (T. mentagrophytes). A new series of twenty-three 3- and 4-arylcoumarins was synthesized and the antifungal activities against clinical isolates of T. rubrum and T. mentagrophytes were evaluated. Sixteen out of twenty-three molecules exhibited antifungal activity against one or both fungi strains. In some cases, the activity against T. rubrum has been comparable to fluconazole, one of the standards, being 8-methoxy-3-(4’-nitrophenyl)coumarin (16) the best compound within this series (minimum inhibitory concentration, MIC=6.25 μg/mL). The preliminary structure-activity relationship study showed that the antifungal activity depends on the position and nature of the substitution patterns. The cytotoxicity of eleven compounds on D-384 (astrocytoma), A-549 (lung cancer) and RKO (colorectal cancer) cell lines was also performed. With the aim of deeply understand the potential of these molecules as hits to develop new drugs, the theoretical absorption, distribution, metabolism and excretion (ADME) properties of the active compounds were calculatedgl
dc.description.peerreviewedSIgl
dc.description.sponsorshipMJM thanks Xunta de Galicia (Galician Plan of Research, Innovation and Growth 2011–2015, Plan I2 C, Grants ED481B 2014/086-0 and ED481B 2018/007), Ministerio de Ciencia e Innovación (PID2020-116076RJ−I00/AEI/10.13039/501100011033) and Fundação para a Ciência e Tecnologia (FCT, CEECIND/02423/2018 and UIDB/00081/2020)gl
dc.identifier.citationChemistrySelect2021,6, 9981–998. https://doi.org/10.1002/slct.202103099gl
dc.identifier.doi10.1002/slct.202103099
dc.identifier.essn2365-6549
dc.identifier.urihttp://hdl.handle.net/10347/29064
dc.language.isoenggl
dc.publisherWileygl
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-116076RJ−I00/ES/CONJUGADOS INNOVADORES RILUZOL-PEPTIDO CAPACES DE CRUZAR LA BARRERA HEMATOENCEFALICAgl
dc.relation.publisherversionhttps://doi.org/10.1002/slct.202103099gl
dc.rights© 2021 The Authors. ChemistrySelect published by Wiley-VCH GmbH. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made Attribution-NonCommercial-NoDerivatives 4.0 Internacionalgl
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAntifungalagentsgl
dc.subjectArylcoumarinsgl
dc.subjectHeterocyclesgl
dc.subjectSynthesisgl
dc.titleStudy of a selected series of 3- and 4-Arylcoumarins as antifungal agents against Dermatophytic Fungi: T. rubrum and T. mentagrophytesgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
relation.isAuthorOfPublication769c5d0c-04c9-43f2-89dc-e4eb770227d5
relation.isAuthorOfPublication.latestForDiscovery769c5d0c-04c9-43f2-89dc-e4eb770227d5

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