Study of a selected series of 3- and 4-Arylcoumarins as antifungal agents against Dermatophytic Fungi: T. rubrum and T. mentagrophytes
Title: | Study of a selected series of 3- and 4-Arylcoumarins as antifungal agents against Dermatophytic Fungi: T. rubrum and T. mentagrophytes
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Author: | López Cisneros, Carmen Lucía
Cazar Ramírez, María Elena
Bailón Moscoso, Natalia
Guardado Yordi, Estela
Borges, Fernanda
Uriarte Villares, Eugenio
Matos, Maria João
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Affiliation: | Universidade de Santiago de Compostela. Departamento de Química Orgánica
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Subject: | Antifungalagents | Arylcoumarins | Heterocycles | Synthesis | |
Date of Issue: | 2021
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Publisher: | Wiley
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Citation: | ChemistrySelect2021,6, 9981–998. https://doi.org/10.1002/slct.202103099
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Abstract: | The 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 calculated |
Publisher version: | https://doi.org/10.1002/slct.202103099 |
URI: | http://hdl.handle.net/10347/29064
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DOI: | 10.1002/slct.202103099 |
E-ISSN: | 2365-6549
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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 Internacional
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