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Assessment of the biological potential of diaryltriazene-derived triazene compounds

In the present study, novel, 1,3-diaryltriazene-derived triazene compounds were synthesized and tested. Triazenes are versatile and belong to a group of alkylating agents with interesting physicochemical properties and proven biological activities. This study describes the synthesis, molecular and c...

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Autores principales: Figueirêdo, Patricia de Maria Silva, Sampaio Filho, José Costa, Sodré, Alzirene de Jesus Sales, de Castro Júnior, José Ribamar, Gonçalves, Ingrid Santos, Blasques, Rodrigo Vieira, S. Correa, Rodrigo, Lima, Benedicto Augusto Vieira, dos Anjos Marques, Larissa, Coutinho, Denise Fernandes, de Azevedo dos Santos, Ana Paula Silva, Luz, Tássio Rômulo Silva Araújo, de Miranda, Rita de Cassia Mendonça, dos Santos, Julliana Ribeiro Alves, Doriguetto, Antonio Carlos, Pividori, María Isabel, Hörner, Manfredo, Villis, Paulo Cesar Mendes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844262/
https://www.ncbi.nlm.nih.gov/pubmed/33510223
http://dx.doi.org/10.1038/s41598-021-81823-2
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author Figueirêdo, Patricia de Maria Silva
Sampaio Filho, José Costa
Sodré, Alzirene de Jesus Sales
de Castro Júnior, José Ribamar
Gonçalves, Ingrid Santos
Blasques, Rodrigo Vieira
S. Correa, Rodrigo
Lima, Benedicto Augusto Vieira
dos Anjos Marques, Larissa
Coutinho, Denise Fernandes
de Azevedo dos Santos, Ana Paula Silva
Luz, Tássio Rômulo Silva Araújo
de Miranda, Rita de Cassia Mendonça
dos Santos, Julliana Ribeiro Alves
Doriguetto, Antonio Carlos
Pividori, María Isabel
Hörner, Manfredo
Villis, Paulo Cesar Mendes
author_facet Figueirêdo, Patricia de Maria Silva
Sampaio Filho, José Costa
Sodré, Alzirene de Jesus Sales
de Castro Júnior, José Ribamar
Gonçalves, Ingrid Santos
Blasques, Rodrigo Vieira
S. Correa, Rodrigo
Lima, Benedicto Augusto Vieira
dos Anjos Marques, Larissa
Coutinho, Denise Fernandes
de Azevedo dos Santos, Ana Paula Silva
Luz, Tássio Rômulo Silva Araújo
de Miranda, Rita de Cassia Mendonça
dos Santos, Julliana Ribeiro Alves
Doriguetto, Antonio Carlos
Pividori, María Isabel
Hörner, Manfredo
Villis, Paulo Cesar Mendes
author_sort Figueirêdo, Patricia de Maria Silva
collection PubMed
description In the present study, novel, 1,3-diaryltriazene-derived triazene compounds were synthesized and tested. Triazenes are versatile and belong to a group of alkylating agents with interesting physicochemical properties and proven biological activities. This study describes the synthesis, molecular and crystalline structure, biological activity evaluation, and antifungal and antimicrobial potentials of 1,3-bis(X-methoxy-Y-nitrophenyl)triazenes [X = 2 and 5; Y = 4 and 5]. The antimicrobial and antifungal activities of the compounds were tested by evaluating the sensitivity of bacteria (American Type Culture Collection, ATCC) and clinical isolates to their solutions using standardized microbiological assays, cytotoxicity evaluation, and ecotoxicity tests. The antimicrobial potentials of triazenes were determined according to their minimum inhibitory concentrations (MICs); these compounds were active against gram-positive and gram-negative bacteria, with low MIC values. The most surprising result was obtained for T3 having the effective MIC of 9.937 µg/mL and antifungal activity against Candida albicans ATCC 90028, C. parapsilosis ATCC 22019, and C. tropicallis IC. To the best of our knowledge, this study is the first to report promising activities of triazene compounds against yeast and filamentous fungi. The results showed the potential utility of triazenes as agents affecting selected resistant bacterial and fungal strains.
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spelling pubmed-78442622021-02-01 Assessment of the biological potential of diaryltriazene-derived triazene compounds Figueirêdo, Patricia de Maria Silva Sampaio Filho, José Costa Sodré, Alzirene de Jesus Sales de Castro Júnior, José Ribamar Gonçalves, Ingrid Santos Blasques, Rodrigo Vieira S. Correa, Rodrigo Lima, Benedicto Augusto Vieira dos Anjos Marques, Larissa Coutinho, Denise Fernandes de Azevedo dos Santos, Ana Paula Silva Luz, Tássio Rômulo Silva Araújo de Miranda, Rita de Cassia Mendonça dos Santos, Julliana Ribeiro Alves Doriguetto, Antonio Carlos Pividori, María Isabel Hörner, Manfredo Villis, Paulo Cesar Mendes Sci Rep Article In the present study, novel, 1,3-diaryltriazene-derived triazene compounds were synthesized and tested. Triazenes are versatile and belong to a group of alkylating agents with interesting physicochemical properties and proven biological activities. This study describes the synthesis, molecular and crystalline structure, biological activity evaluation, and antifungal and antimicrobial potentials of 1,3-bis(X-methoxy-Y-nitrophenyl)triazenes [X = 2 and 5; Y = 4 and 5]. The antimicrobial and antifungal activities of the compounds were tested by evaluating the sensitivity of bacteria (American Type Culture Collection, ATCC) and clinical isolates to their solutions using standardized microbiological assays, cytotoxicity evaluation, and ecotoxicity tests. The antimicrobial potentials of triazenes were determined according to their minimum inhibitory concentrations (MICs); these compounds were active against gram-positive and gram-negative bacteria, with low MIC values. The most surprising result was obtained for T3 having the effective MIC of 9.937 µg/mL and antifungal activity against Candida albicans ATCC 90028, C. parapsilosis ATCC 22019, and C. tropicallis IC. To the best of our knowledge, this study is the first to report promising activities of triazene compounds against yeast and filamentous fungi. The results showed the potential utility of triazenes as agents affecting selected resistant bacterial and fungal strains. Nature Publishing Group UK 2021-01-28 /pmc/articles/PMC7844262/ /pubmed/33510223 http://dx.doi.org/10.1038/s41598-021-81823-2 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Figueirêdo, Patricia de Maria Silva
Sampaio Filho, José Costa
Sodré, Alzirene de Jesus Sales
de Castro Júnior, José Ribamar
Gonçalves, Ingrid Santos
Blasques, Rodrigo Vieira
S. Correa, Rodrigo
Lima, Benedicto Augusto Vieira
dos Anjos Marques, Larissa
Coutinho, Denise Fernandes
de Azevedo dos Santos, Ana Paula Silva
Luz, Tássio Rômulo Silva Araújo
de Miranda, Rita de Cassia Mendonça
dos Santos, Julliana Ribeiro Alves
Doriguetto, Antonio Carlos
Pividori, María Isabel
Hörner, Manfredo
Villis, Paulo Cesar Mendes
Assessment of the biological potential of diaryltriazene-derived triazene compounds
title Assessment of the biological potential of diaryltriazene-derived triazene compounds
title_full Assessment of the biological potential of diaryltriazene-derived triazene compounds
title_fullStr Assessment of the biological potential of diaryltriazene-derived triazene compounds
title_full_unstemmed Assessment of the biological potential of diaryltriazene-derived triazene compounds
title_short Assessment of the biological potential of diaryltriazene-derived triazene compounds
title_sort assessment of the biological potential of diaryltriazene-derived triazene compounds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844262/
https://www.ncbi.nlm.nih.gov/pubmed/33510223
http://dx.doi.org/10.1038/s41598-021-81823-2
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