SÍNTESE DE POTENCIAIS MARCADORES CELULARES A PARTIR DA REAÇÃO DE INDÓIS N-SUBSTITUÍDOS COM A 1,4-NAFTOQUINONA

Detalhes bibliográficos
Autor(a) principal: Ingrid Duarte Pereira
Data de Publicação: 2023
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UFMS
Texto Completo: https://repositorio.ufms.br/handle/123456789/8235
Resumo: Indoles and quinones are classes of compounds that have been widely studied because they have different biological activities, such as antitumor, antidiabetic, and leishmanicidal activity, among others. The literature demonstrates that when these two classes of compounds react, the products formed continue to show biological activity and, in some cases, fluorescence. This characteristic is observed, for example, in polycyclic compounds containing heteroatoms, highly conjugated π systems and rigid structures. This work aims to synthesize fluorescent compounds through reactions between different indoles and 1,4-naphthoquinone and to evaluate their potential application as fluorescent probes in living cells. Several reactions were carried out to optimize the process of obtaining the derivatives, varying the solvent, molar equivalents of the reactants, temperature and reaction time. Using the best conditions, two derivatives were obtained in the coupling reaction of 1-methyl-1H-indole and 1,4-naphthoquinone in the presence of acetic acid as a solvent. The two compounds obtained had their spectroscopic properties in the UV/Vis region and fluorescence evaluated, and initial tests were also carried out for their application as labeling probes in live cells. In the current stage of the research, indoles are being prepared, already described in the literature, to be used later in the coupling reaction with 1,4-naphthoquinone, thus allowing the synthesis of new compounds. The experiments carried out and the vast applicability of these compounds encourage the continuity of research in the process of obtaining the derivatives.
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spelling 2023-12-27T21:08:39Z2023-12-27T21:08:39Z2023https://repositorio.ufms.br/handle/123456789/8235Indoles and quinones are classes of compounds that have been widely studied because they have different biological activities, such as antitumor, antidiabetic, and leishmanicidal activity, among others. The literature demonstrates that when these two classes of compounds react, the products formed continue to show biological activity and, in some cases, fluorescence. This characteristic is observed, for example, in polycyclic compounds containing heteroatoms, highly conjugated π systems and rigid structures. This work aims to synthesize fluorescent compounds through reactions between different indoles and 1,4-naphthoquinone and to evaluate their potential application as fluorescent probes in living cells. Several reactions were carried out to optimize the process of obtaining the derivatives, varying the solvent, molar equivalents of the reactants, temperature and reaction time. Using the best conditions, two derivatives were obtained in the coupling reaction of 1-methyl-1H-indole and 1,4-naphthoquinone in the presence of acetic acid as a solvent. The two compounds obtained had their spectroscopic properties in the UV/Vis region and fluorescence evaluated, and initial tests were also carried out for their application as labeling probes in live cells. In the current stage of the research, indoles are being prepared, already described in the literature, to be used later in the coupling reaction with 1,4-naphthoquinone, thus allowing the synthesis of new compounds. The experiments carried out and the vast applicability of these compounds encourage the continuity of research in the process of obtaining the derivatives.Indóis e quinonas são classes de compostos amplamente estudados por apresentarem diversas atividades biológicas, como atividade antitumoral, antidiabética, leishimanicida, dentre outras. A literatura demonstra que quando essas duas classes de compostos reagem, os produtos formados continuam apresentando atividade biológica e em alguns casos fluorescência. Essa característica é observada, por exemplo, em compostos policíclicos contendo heteroátomos, sistemas π altamente conjugados e estruturas rígidas. Este trabalho tem como objetivo a síntese de compostos fluorescentes por meio de reações entre diferentes indóis e a 1,4-naftoquinona e, avaliar o potencial de aplicação como sondas fluorescentes em células vivas. Foram realizadas diversas reações para a otimização do processo de obtenção dos derivados, variando o solvente, equivalências molares dos reagentes, temperatura e tempo reacional. Por meio do uso das melhores condições, foram obtidos dois derivados na reação de acoplamento do 1-metil-1H- indol e da 1,4-naftoquinona em presença de ácido acético como solvente. Os dois compostos obtidos tiveram as suas propriedades espectroscópicas na região do UV/Vis e fluorescência avaliados, e também foram realizados ensaios iniciais de aplicação como sondas de marcação em células vivas. Na etapa atual da pesquisa estão sendo preparados indóis, já descritos na literatura, para serem utilizados posteriormente na reação de acoplamento com a 1,4- naftoquinona, permitindo assim a síntese de compostos inéditos. Os experimentos realizados e a vasta aplicabilidade destes compostos encorajam para a continuidade da pesquisa no processo de obtenção dos derivados.Fundação Universidade Federal de Mato Grosso do SulUFMSBrasilIndolNaftoquinonaantitumoralfluorescênciamarcadores celularesSÍNTESE DE POTENCIAIS MARCADORES CELULARES A PARTIR DA REAÇÃO DE INDÓIS N-SUBSTITUÍDOS COM A 1,4-NAFTOQUINONAinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisEdson dos Anjos dos SantosIngrid Duarte Pereirainfo:eu-repo/semantics/openAccessporreponame:Repositório Institucional da UFMSinstname:Universidade Federal de Mato Grosso do Sul (UFMS)instacron:UFMSORIGINALTese Ingrid D Pereira.pdfTese Ingrid D Pereira.pdfapplication/pdf3873392https://repositorio.ufms.br/bitstream/123456789/8235/-1/Tese%20Ingrid%20D%20Pereira.pdfbe7d724a5291c873a6c049a6c2e2b794MD5-1123456789/82352023-12-27 17:08:40.351oai:repositorio.ufms.br:123456789/8235Repositório InstitucionalPUBhttps://repositorio.ufms.br/oai/requestri.prograd@ufms.bropendoar:21242023-12-27T21:08:40Repositório Institucional da UFMS - Universidade Federal de Mato Grosso do Sul (UFMS)false
dc.title.pt_BR.fl_str_mv SÍNTESE DE POTENCIAIS MARCADORES CELULARES A PARTIR DA REAÇÃO DE INDÓIS N-SUBSTITUÍDOS COM A 1,4-NAFTOQUINONA
title SÍNTESE DE POTENCIAIS MARCADORES CELULARES A PARTIR DA REAÇÃO DE INDÓIS N-SUBSTITUÍDOS COM A 1,4-NAFTOQUINONA
spellingShingle SÍNTESE DE POTENCIAIS MARCADORES CELULARES A PARTIR DA REAÇÃO DE INDÓIS N-SUBSTITUÍDOS COM A 1,4-NAFTOQUINONA
Ingrid Duarte Pereira
Indol
Naftoquinona
antitumoral
fluorescência
marcadores celulares
title_short SÍNTESE DE POTENCIAIS MARCADORES CELULARES A PARTIR DA REAÇÃO DE INDÓIS N-SUBSTITUÍDOS COM A 1,4-NAFTOQUINONA
title_full SÍNTESE DE POTENCIAIS MARCADORES CELULARES A PARTIR DA REAÇÃO DE INDÓIS N-SUBSTITUÍDOS COM A 1,4-NAFTOQUINONA
title_fullStr SÍNTESE DE POTENCIAIS MARCADORES CELULARES A PARTIR DA REAÇÃO DE INDÓIS N-SUBSTITUÍDOS COM A 1,4-NAFTOQUINONA
title_full_unstemmed SÍNTESE DE POTENCIAIS MARCADORES CELULARES A PARTIR DA REAÇÃO DE INDÓIS N-SUBSTITUÍDOS COM A 1,4-NAFTOQUINONA
title_sort SÍNTESE DE POTENCIAIS MARCADORES CELULARES A PARTIR DA REAÇÃO DE INDÓIS N-SUBSTITUÍDOS COM A 1,4-NAFTOQUINONA
author Ingrid Duarte Pereira
author_facet Ingrid Duarte Pereira
author_role author
dc.contributor.advisor1.fl_str_mv Edson dos Anjos dos Santos
dc.contributor.author.fl_str_mv Ingrid Duarte Pereira
contributor_str_mv Edson dos Anjos dos Santos
dc.subject.por.fl_str_mv Indol
Naftoquinona
antitumoral
fluorescência
marcadores celulares
topic Indol
Naftoquinona
antitumoral
fluorescência
marcadores celulares
description Indoles and quinones are classes of compounds that have been widely studied because they have different biological activities, such as antitumor, antidiabetic, and leishmanicidal activity, among others. The literature demonstrates that when these two classes of compounds react, the products formed continue to show biological activity and, in some cases, fluorescence. This characteristic is observed, for example, in polycyclic compounds containing heteroatoms, highly conjugated π systems and rigid structures. This work aims to synthesize fluorescent compounds through reactions between different indoles and 1,4-naphthoquinone and to evaluate their potential application as fluorescent probes in living cells. Several reactions were carried out to optimize the process of obtaining the derivatives, varying the solvent, molar equivalents of the reactants, temperature and reaction time. Using the best conditions, two derivatives were obtained in the coupling reaction of 1-methyl-1H-indole and 1,4-naphthoquinone in the presence of acetic acid as a solvent. The two compounds obtained had their spectroscopic properties in the UV/Vis region and fluorescence evaluated, and initial tests were also carried out for their application as labeling probes in live cells. In the current stage of the research, indoles are being prepared, already described in the literature, to be used later in the coupling reaction with 1,4-naphthoquinone, thus allowing the synthesis of new compounds. The experiments carried out and the vast applicability of these compounds encourage the continuity of research in the process of obtaining the derivatives.
publishDate 2023
dc.date.accessioned.fl_str_mv 2023-12-27T21:08:39Z
dc.date.available.fl_str_mv 2023-12-27T21:08:39Z
dc.date.issued.fl_str_mv 2023
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
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dc.identifier.uri.fl_str_mv https://repositorio.ufms.br/handle/123456789/8235
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dc.publisher.none.fl_str_mv Fundação Universidade Federal de Mato Grosso do Sul
dc.publisher.initials.fl_str_mv UFMS
dc.publisher.country.fl_str_mv Brasil
publisher.none.fl_str_mv Fundação Universidade Federal de Mato Grosso do Sul
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFMS
instname:Universidade Federal de Mato Grosso do Sul (UFMS)
instacron:UFMS
instname_str Universidade Federal de Mato Grosso do Sul (UFMS)
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institution UFMS
reponame_str Repositório Institucional da UFMS
collection Repositório Institucional da UFMS
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