Synthesis and Evaluation of the Antifungal and Toxicological Activity of Nitrofuran Derivatives

Detalhes bibliográficos
Autor(a) principal: Vaso, Carolina Orlando [UNESP]
Data de Publicação: 2022
Outros Autores: Pandolfi, Fabiana, Bila, Níura Madalena [UNESP], De Vita, Daniela, Bortolami, Martina, Mendes-Giannini, Maria José Soares [UNESP], Tudino, Valeria, Costi, Roberta, Costa-Orlandi, Caroline Barcelos [UNESP], Fusco-Almeida, Ana Marisa [UNESP], Scipione, Luigi
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/pharmaceutics14030593
http://hdl.handle.net/11449/234270
Resumo: Fungal diseases affect more than 1 billion people worldwide. The constant global changes, the advent of new pandemics, and chronic diseases favor the diffusion of fungal pathogens such as Candida, Cryptococcus, Aspergillus, Trichophyton, Histoplasma capsulatum, and Paracoccidioides brasiliensis. In this work, a series of nitrofuran derivatives were synthesized and tested against different fungal species; most of them showed inhibitory activity, fungicide, and fungistatic profile. The minimal inhibitory concentration (MIC90) values for the most potent compounds range from 0.48 μg/mL against H. capsulatum (compound 11) and P. brasiliensis (compounds 3 and 9) to 0.98 μg/mL against Trichophyton rubrum and T. mentagrophytes (compounds 8, 9, 12, 13 and 8, 12, 13, respectively), and 3.9 μg/mL against Candida and Cryptococcus neoformans strains (compounds 1 and 5, respectively). In addition, all compounds showed low toxicity when tested in vitro on lung cell lines (A549 and MRC-5) and in vivo in Caenorhabditis elegans larvae. Many of them showed high selectivity index values. Thus, these studied nitrofuran derivatives proved to be potent against different fungal species, characterized by low toxicity and high selectivity; for these reasons, they may become promising compounds for the treatment of mycoses.
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spelling Synthesis and Evaluation of the Antifungal and Toxicological Activity of Nitrofuran DerivativesAntifungal activityBroad-spectrum antifungalCaenorhabditis elegans larvaeCandida spCryptococcus neoformansHistoplasma capsulatumNitrofuran derivatesParacoccidioides brasiliensisTrichophyton mentagrophytesTrichophyton rubrumFungal diseases affect more than 1 billion people worldwide. The constant global changes, the advent of new pandemics, and chronic diseases favor the diffusion of fungal pathogens such as Candida, Cryptococcus, Aspergillus, Trichophyton, Histoplasma capsulatum, and Paracoccidioides brasiliensis. In this work, a series of nitrofuran derivatives were synthesized and tested against different fungal species; most of them showed inhibitory activity, fungicide, and fungistatic profile. The minimal inhibitory concentration (MIC90) values for the most potent compounds range from 0.48 μg/mL against H. capsulatum (compound 11) and P. brasiliensis (compounds 3 and 9) to 0.98 μg/mL against Trichophyton rubrum and T. mentagrophytes (compounds 8, 9, 12, 13 and 8, 12, 13, respectively), and 3.9 μg/mL against Candida and Cryptococcus neoformans strains (compounds 1 and 5, respectively). In addition, all compounds showed low toxicity when tested in vitro on lung cell lines (A549 and MRC-5) and in vivo in Caenorhabditis elegans larvae. Many of them showed high selectivity index values. Thus, these studied nitrofuran derivatives proved to be potent against different fungal species, characterized by low toxicity and high selectivity; for these reasons, they may become promising compounds for the treatment of mycoses.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)School of Pharmaceutical Science Universidade Estadual Paulista, SPDepartment of Scienze di Base e Applicate per l’Ingegneria Sapienza University of Rome, Via Castro Laurenziano 7Department of Environmental Biology Sapienza University of Rome, Piazzale Aldo Moro 5Department of Chimica e Tecnologia del Farmaco Sapienza University of Rome, Piazzale Aldo MoroDepartment of Chemistry and Technology of Drug Instituto Pasteur Fondazione Cenci Bolognetti Sapienza University of Rome, Piazzale Aldo Moro 5School of Pharmaceutical Science Universidade Estadual Paulista, SPCAPES: 001CNPq: 134559/2018-5CNPq: 142049/2019-0FAPESP: 16/11836-0FAPESP: 2017/18388-6FAPESP: 2019/22188-8FAPESP: 2020/15586-4CAPES: 88887.500765/2020-00Universidade Estadual Paulista (UNESP)Sapienza University of RomeVaso, Carolina Orlando [UNESP]Pandolfi, FabianaBila, Níura Madalena [UNESP]De Vita, DanielaBortolami, MartinaMendes-Giannini, Maria José Soares [UNESP]Tudino, ValeriaCosti, RobertaCosta-Orlandi, Caroline Barcelos [UNESP]Fusco-Almeida, Ana Marisa [UNESP]Scipione, Luigi2022-05-01T15:30:01Z2022-05-01T15:30:01Z2022-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/pharmaceutics14030593Pharmaceutics, v. 14, n. 3, 2022.1999-4923http://hdl.handle.net/11449/23427010.3390/pharmaceutics140305932-s2.0-85126453264Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPharmaceuticsinfo:eu-repo/semantics/openAccess2024-06-21T15:19:21Zoai:repositorio.unesp.br:11449/234270Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:43:44.579240Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Synthesis and Evaluation of the Antifungal and Toxicological Activity of Nitrofuran Derivatives
title Synthesis and Evaluation of the Antifungal and Toxicological Activity of Nitrofuran Derivatives
spellingShingle Synthesis and Evaluation of the Antifungal and Toxicological Activity of Nitrofuran Derivatives
Vaso, Carolina Orlando [UNESP]
Antifungal activity
Broad-spectrum antifungal
Caenorhabditis elegans larvae
Candida sp
Cryptococcus neoformans
Histoplasma capsulatum
Nitrofuran derivates
Paracoccidioides brasiliensis
Trichophyton mentagrophytes
Trichophyton rubrum
title_short Synthesis and Evaluation of the Antifungal and Toxicological Activity of Nitrofuran Derivatives
title_full Synthesis and Evaluation of the Antifungal and Toxicological Activity of Nitrofuran Derivatives
title_fullStr Synthesis and Evaluation of the Antifungal and Toxicological Activity of Nitrofuran Derivatives
title_full_unstemmed Synthesis and Evaluation of the Antifungal and Toxicological Activity of Nitrofuran Derivatives
title_sort Synthesis and Evaluation of the Antifungal and Toxicological Activity of Nitrofuran Derivatives
author Vaso, Carolina Orlando [UNESP]
author_facet Vaso, Carolina Orlando [UNESP]
Pandolfi, Fabiana
Bila, Níura Madalena [UNESP]
De Vita, Daniela
Bortolami, Martina
Mendes-Giannini, Maria José Soares [UNESP]
Tudino, Valeria
Costi, Roberta
Costa-Orlandi, Caroline Barcelos [UNESP]
Fusco-Almeida, Ana Marisa [UNESP]
Scipione, Luigi
author_role author
author2 Pandolfi, Fabiana
Bila, Níura Madalena [UNESP]
De Vita, Daniela
Bortolami, Martina
Mendes-Giannini, Maria José Soares [UNESP]
Tudino, Valeria
Costi, Roberta
Costa-Orlandi, Caroline Barcelos [UNESP]
Fusco-Almeida, Ana Marisa [UNESP]
Scipione, Luigi
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Sapienza University of Rome
dc.contributor.author.fl_str_mv Vaso, Carolina Orlando [UNESP]
Pandolfi, Fabiana
Bila, Níura Madalena [UNESP]
De Vita, Daniela
Bortolami, Martina
Mendes-Giannini, Maria José Soares [UNESP]
Tudino, Valeria
Costi, Roberta
Costa-Orlandi, Caroline Barcelos [UNESP]
Fusco-Almeida, Ana Marisa [UNESP]
Scipione, Luigi
dc.subject.por.fl_str_mv Antifungal activity
Broad-spectrum antifungal
Caenorhabditis elegans larvae
Candida sp
Cryptococcus neoformans
Histoplasma capsulatum
Nitrofuran derivates
Paracoccidioides brasiliensis
Trichophyton mentagrophytes
Trichophyton rubrum
topic Antifungal activity
Broad-spectrum antifungal
Caenorhabditis elegans larvae
Candida sp
Cryptococcus neoformans
Histoplasma capsulatum
Nitrofuran derivates
Paracoccidioides brasiliensis
Trichophyton mentagrophytes
Trichophyton rubrum
description Fungal diseases affect more than 1 billion people worldwide. The constant global changes, the advent of new pandemics, and chronic diseases favor the diffusion of fungal pathogens such as Candida, Cryptococcus, Aspergillus, Trichophyton, Histoplasma capsulatum, and Paracoccidioides brasiliensis. In this work, a series of nitrofuran derivatives were synthesized and tested against different fungal species; most of them showed inhibitory activity, fungicide, and fungistatic profile. The minimal inhibitory concentration (MIC90) values for the most potent compounds range from 0.48 μg/mL against H. capsulatum (compound 11) and P. brasiliensis (compounds 3 and 9) to 0.98 μg/mL against Trichophyton rubrum and T. mentagrophytes (compounds 8, 9, 12, 13 and 8, 12, 13, respectively), and 3.9 μg/mL against Candida and Cryptococcus neoformans strains (compounds 1 and 5, respectively). In addition, all compounds showed low toxicity when tested in vitro on lung cell lines (A549 and MRC-5) and in vivo in Caenorhabditis elegans larvae. Many of them showed high selectivity index values. Thus, these studied nitrofuran derivatives proved to be potent against different fungal species, characterized by low toxicity and high selectivity; for these reasons, they may become promising compounds for the treatment of mycoses.
publishDate 2022
dc.date.none.fl_str_mv 2022-05-01T15:30:01Z
2022-05-01T15:30:01Z
2022-03-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.3390/pharmaceutics14030593
Pharmaceutics, v. 14, n. 3, 2022.
1999-4923
http://hdl.handle.net/11449/234270
10.3390/pharmaceutics14030593
2-s2.0-85126453264
url http://dx.doi.org/10.3390/pharmaceutics14030593
http://hdl.handle.net/11449/234270
identifier_str_mv Pharmaceutics, v. 14, n. 3, 2022.
1999-4923
10.3390/pharmaceutics14030593
2-s2.0-85126453264
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Pharmaceutics
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
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instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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