Synthesis, characterization and preliminary antibacterial evaluation against Staphylococcus aureus of a new 2,4,5-tri(hetero)arylimidazole derivative based on azaindole heterocycle
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://hdl.handle.net/1822/74801 |
Resumo: | Imidazole derivatives are known for their numerous biological applications, such as antibacterial, antifungal, antioxidant, antiviral, antiparasitic and anticancer, among others. Therefore, several imidazole derivatives have been synthesized and developed in recent years as potential drugs in the treatment of several diseases. In this communication, we report the synthesis of a new imidazole derivative, substituted at positions 2, 4 and 5 with heterocyclic groups, using a simple synthetic methodology and an easy purification procedure. The new compound was characterized by the usual spectroscopic techniques (NMR, UV-Vis absorption and emission). The evaluation of the novel imidazole derivative as a potential antibiotic drug was carried out against the Gram-positive bacterium Staphylococcus aureus, using disk test diffusion method. Results showed a dose-response effect against the bacteria under study, revealing that the rational design of this imidazole derivative is quite promising to improve antibacterial activity of imidazole derivatives. |
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Synthesis, characterization and preliminary antibacterial evaluation against Staphylococcus aureus of a new 2,4,5-tri(hetero)arylimidazole derivative based on azaindole heterocycleImidazoleSynthesisAntibacterial activityStaphylococcus aureusImidazole derivatives are known for their numerous biological applications, such as antibacterial, antifungal, antioxidant, antiviral, antiparasitic and anticancer, among others. Therefore, several imidazole derivatives have been synthesized and developed in recent years as potential drugs in the treatment of several diseases. In this communication, we report the synthesis of a new imidazole derivative, substituted at positions 2, 4 and 5 with heterocyclic groups, using a simple synthetic methodology and an easy purification procedure. The new compound was characterized by the usual spectroscopic techniques (NMR, UV-Vis absorption and emission). The evaluation of the novel imidazole derivative as a potential antibiotic drug was carried out against the Gram-positive bacterium Staphylococcus aureus, using disk test diffusion method. Results showed a dose-response effect against the bacteria under study, revealing that the rational design of this imidazole derivative is quite promising to improve antibacterial activity of imidazole derivatives.This research was funded by the Foundation for Science and Technology (FCT) through CQ/UM (UIDB/00686/2020) and CBMA/UM “Contrato-Programa” UIDB/04050/2020 funded by national funds. Thanks are also due to FCT for financial support to the Portuguese NMR Network (PTNMR, Bruker Avance III 400-Univ. Minho).info:eu-repo/semantics/publishedVersionMDPIUniversidade do MinhoRamos, Nuna Liliana PereiraOliveira, Rui Pedro Soares deCosta, Susana P. G.Raposo, M. Manuela M.20222022-01-01T00:00:00Zconference paperinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://hdl.handle.net/1822/74801https://creativecommons.org/licenses/by/4.0/reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPengRamos, N.L.P.; Oliveira, R.; Costa, S.P.G.; Raposo, M.M.M. Synthesis, Characterization and Preliminary Antibacterial Evaluation against Staphylococcus aureus of a New 2,4,5-Tri(hetero)arylimidazole Derivative Based on Azaindole Heterocycle. Chem. Proc. 2022, 8, 104. https://doi.org/10.3390/ecsoc-25-117812673-458310.3390/ecsoc-25-11781https://www.mdpi.com/2673-4583/8/1/104info:eu-repo/semantics/openAccess2024-05-11T07:25:46Zoai:repositorium.sdum.uminho.pt:1822/74801Portal AgregadorONGhttps://www.rcaap.pt/oai/openairemluisa.alvim@gmail.comopendoar:71602024-05-11T07:25:46Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Synthesis, characterization and preliminary antibacterial evaluation against Staphylococcus aureus of a new 2,4,5-tri(hetero)arylimidazole derivative based on azaindole heterocycle |
title |
Synthesis, characterization and preliminary antibacterial evaluation against Staphylococcus aureus of a new 2,4,5-tri(hetero)arylimidazole derivative based on azaindole heterocycle |
spellingShingle |
Synthesis, characterization and preliminary antibacterial evaluation against Staphylococcus aureus of a new 2,4,5-tri(hetero)arylimidazole derivative based on azaindole heterocycle Ramos, Nuna Liliana Pereira Imidazole Synthesis Antibacterial activity Staphylococcus aureus |
title_short |
Synthesis, characterization and preliminary antibacterial evaluation against Staphylococcus aureus of a new 2,4,5-tri(hetero)arylimidazole derivative based on azaindole heterocycle |
title_full |
Synthesis, characterization and preliminary antibacterial evaluation against Staphylococcus aureus of a new 2,4,5-tri(hetero)arylimidazole derivative based on azaindole heterocycle |
title_fullStr |
Synthesis, characterization and preliminary antibacterial evaluation against Staphylococcus aureus of a new 2,4,5-tri(hetero)arylimidazole derivative based on azaindole heterocycle |
title_full_unstemmed |
Synthesis, characterization and preliminary antibacterial evaluation against Staphylococcus aureus of a new 2,4,5-tri(hetero)arylimidazole derivative based on azaindole heterocycle |
title_sort |
Synthesis, characterization and preliminary antibacterial evaluation against Staphylococcus aureus of a new 2,4,5-tri(hetero)arylimidazole derivative based on azaindole heterocycle |
author |
Ramos, Nuna Liliana Pereira |
author_facet |
Ramos, Nuna Liliana Pereira Oliveira, Rui Pedro Soares de Costa, Susana P. G. Raposo, M. Manuela M. |
author_role |
author |
author2 |
Oliveira, Rui Pedro Soares de Costa, Susana P. G. Raposo, M. Manuela M. |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Ramos, Nuna Liliana Pereira Oliveira, Rui Pedro Soares de Costa, Susana P. G. Raposo, M. Manuela M. |
dc.subject.por.fl_str_mv |
Imidazole Synthesis Antibacterial activity Staphylococcus aureus |
topic |
Imidazole Synthesis Antibacterial activity Staphylococcus aureus |
description |
Imidazole derivatives are known for their numerous biological applications, such as antibacterial, antifungal, antioxidant, antiviral, antiparasitic and anticancer, among others. Therefore, several imidazole derivatives have been synthesized and developed in recent years as potential drugs in the treatment of several diseases. In this communication, we report the synthesis of a new imidazole derivative, substituted at positions 2, 4 and 5 with heterocyclic groups, using a simple synthetic methodology and an easy purification procedure. The new compound was characterized by the usual spectroscopic techniques (NMR, UV-Vis absorption and emission). The evaluation of the novel imidazole derivative as a potential antibiotic drug was carried out against the Gram-positive bacterium Staphylococcus aureus, using disk test diffusion method. Results showed a dose-response effect against the bacteria under study, revealing that the rational design of this imidazole derivative is quite promising to improve antibacterial activity of imidazole derivatives. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022 2022-01-01T00:00:00Z |
dc.type.driver.fl_str_mv |
conference paper |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/1822/74801 |
url |
https://hdl.handle.net/1822/74801 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Ramos, N.L.P.; Oliveira, R.; Costa, S.P.G.; Raposo, M.M.M. Synthesis, Characterization and Preliminary Antibacterial Evaluation against Staphylococcus aureus of a New 2,4,5-Tri(hetero)arylimidazole Derivative Based on Azaindole Heterocycle. Chem. Proc. 2022, 8, 104. https://doi.org/10.3390/ecsoc-25-11781 2673-4583 10.3390/ecsoc-25-11781 https://www.mdpi.com/2673-4583/8/1/104 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
MDPI |
publisher.none.fl_str_mv |
MDPI |
dc.source.none.fl_str_mv |
https://creativecommons.org/licenses/by/4.0/ reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
mluisa.alvim@gmail.com |
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1817545313204830208 |