Síntese e avaliação biológica de ésteres derivados do borneol 

Detalhes bibliográficos
Ano de defesa: 2014
Autor(a) principal: Aline Teixeira Maciel e Silva
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Minas Gerais
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: https://hdl.handle.net/1843/SFSA-9JTSGH
Resumo: The terpenes and its derivatives represent compounds of great interest to researchers because of the great potential as a source of new drugs. In this work, esters from the terpene borneol were synthesized using two methodologies (DIC/DMAP and SOCl2). It was also evaluated the microwave irradiation to obtain these compounds, without the use of solvent. It was synthesized 20 borneol esters, among them 18 are not described in the literature. Some of the reactions conducted under microwave irradiation and in the absence of solvent, led to products of rearrangement. The borneol esters had their structures elucidated through spectroscopic and spectrometric methods. The reaction condition in which were used DIC/DMAP and microwave irradiation, in less time produced better yields. The synthesized compounds were subjected to assays to evaluate its activity as antimicrobial, leishmanicidal, cellular antiproliferation and anti-inflammatory. The best results on the antimicrobial assays were found for bornyl 4-methoxybenzoate, bornyl 3,4-dimethoxybenzoate and bornyl 3,4,5-trimethoxybenzoate. It was not observed significative leishmanicidal effect produced by the borneol esters subjected to assay. In relation to the antiproliferative cells assays, bornyl octanoate, bornyl benzoate and bornyl 3,4,5-trimethoxybenzoate showed more promising results, with cytotoxic effects to cell lines of ovarian cancer (OVCAR-3), ovarian-resistant (NCI-ADR/RES), breast (MCF-7), bone marrow (K562) and kidney (786-0). In the anti-inflammatory assays, the bornyl hexanoate, bornyl octanoate, bornyl tetradecanoate, bornyl hexadecanoate, bornyl octadecanoate, bornyl benzoate, bornyl 3,5-dinitrobenzoate and bornyl nicotinate were those that provided better reduction in the edema induced by carrageenin.
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spelling 2019-08-10T16:40:40Z2025-09-08T23:35:51Z2019-08-10T16:40:40Z2014-02-24https://hdl.handle.net/1843/SFSA-9JTSGHThe terpenes and its derivatives represent compounds of great interest to researchers because of the great potential as a source of new drugs. In this work, esters from the terpene borneol were synthesized using two methodologies (DIC/DMAP and SOCl2). It was also evaluated the microwave irradiation to obtain these compounds, without the use of solvent. It was synthesized 20 borneol esters, among them 18 are not described in the literature. Some of the reactions conducted under microwave irradiation and in the absence of solvent, led to products of rearrangement. The borneol esters had their structures elucidated through spectroscopic and spectrometric methods. The reaction condition in which were used DIC/DMAP and microwave irradiation, in less time produced better yields. The synthesized compounds were subjected to assays to evaluate its activity as antimicrobial, leishmanicidal, cellular antiproliferation and anti-inflammatory. The best results on the antimicrobial assays were found for bornyl 4-methoxybenzoate, bornyl 3,4-dimethoxybenzoate and bornyl 3,4,5-trimethoxybenzoate. It was not observed significative leishmanicidal effect produced by the borneol esters subjected to assay. In relation to the antiproliferative cells assays, bornyl octanoate, bornyl benzoate and bornyl 3,4,5-trimethoxybenzoate showed more promising results, with cytotoxic effects to cell lines of ovarian cancer (OVCAR-3), ovarian-resistant (NCI-ADR/RES), breast (MCF-7), bone marrow (K562) and kidney (786-0). In the anti-inflammatory assays, the bornyl hexanoate, bornyl octanoate, bornyl tetradecanoate, bornyl hexadecanoate, bornyl octadecanoate, bornyl benzoate, bornyl 3,5-dinitrobenzoate and bornyl nicotinate were those that provided better reduction in the edema induced by carrageenin.Universidade Federal de Minas GeraisTerpeno borneolAtividade antimicrobianaTerpenosÉsteres do borneolLeishmanicidaAntiproliferação celular e antiinflamatórioMicro-ondasQuímica OrgânicaSíntese orgânicaProdutos naturaisEsteresSíntese e avaliação biológica de ésteres derivados do borneol info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisAline Teixeira Maciel e Silvainfo:eu-repo/semantics/openAccessporreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMGGracia Divina de Fatima SilvaRoqueline Rodrigues Silva de MirandaMarcelo Moreira BrittoHenriete da Silva VieiraOs terpenos e seus derivados representam compostos de grande interesse para os pesquisadores em função do grande potencial como fonte de novos fármacos. Neste trabalho foram sintetizados ésteres a partir do terpeno borneol utilizando duas metodologias (DIC/DMAP e SOCl2). Também foi avaliada a irradiação de microondas, para obter estes compostos, em ausência de solvente. Foram sintetizados 20 ésteres do borneol, dentre eles 18 não estão descritos na literatura. Algumas das reações conduzidas sob irradiação com micro-ondas e na ausência de solvente levaram a produtos de rearranjo. Os ésteres do borneol tiveram suas estruturas elucidadas através de métodos espectrométricos e espectroscópicos. O meio reacional no qual se utilizou DIC/DMAP e irradiação de micro-ondas, em menor tempo proporcionou os melhores rendimentos. Os compostos sintetizados foram submetidos a testes de avaliação de sua atividade como antimicrobiano, leishmanicida, antiproliferação celular e antiinflamatório. Os melhores resultados no teste antimicrobiano foram encontrados para 4'-metoxibenzoato de bornila, 3',4'-dimetoxibenzoato de bornila e 3',4',5'-trimetoxibenzoato de bornila. Não foi observado nenhum efeito leishmanicida significativo produzido pelos ésteres do borneol submetidos ao teste. Em relação à atividade antiproliferativa, os compostos octanoato de bornila, benzoato de bornila e 3',4',5'-trimetoxibenzoato de bornila apresentaram resultados mais promissores, com efeitos citotóxicos para as linhagens de células de câncer de ovário (OVCAR-3), ovárioresistente (NCI-ADR/RES), mama (MCF-7), medula óssea (K562) e rim (786-0). No teste de atividade anti-inflamatória, o hexanoato de bornila, octanoato de bornila, tetradecanoato de bornila, hexadecanoato de bornila, octadecanoato de bornila, benzoato de bornila, 3',5'-dinitrobenzoato de bornila e nicotinato de bornila foram aqueles que proporcionaram melhor redução do edema induzido por carragenina.UFMGORIGINALdissertacao_final_aline.pdfapplication/pdf8674377https://repositorio.ufmg.br//bitstreams/c53ed79d-4dbb-4f77-b1d7-6e87045a21a9/download46a0c610a1ab66bc86a8c6559ba9034bMD51trueAnonymousREADTEXTdissertacao_final_aline.pdf.txttext/plain244253https://repositorio.ufmg.br//bitstreams/8cf55737-40de-4c12-b7c0-a5a4f9bb40a2/downloadffdfc8ff66d0407ae1531728d912e5beMD52falseAnonymousREAD1843/SFSA-9JTSGH2025-09-08 20:35:51.345open.accessoai:repositorio.ufmg.br:1843/SFSA-9JTSGHhttps://repositorio.ufmg.br/Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2025-09-08T23:35:51Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false
dc.title.none.fl_str_mv Síntese e avaliação biológica de ésteres derivados do borneol 
title Síntese e avaliação biológica de ésteres derivados do borneol 
spellingShingle Síntese e avaliação biológica de ésteres derivados do borneol 
Aline Teixeira Maciel e Silva
Química Orgânica
Síntese orgânica
Produtos naturais
Esteres
Terpeno borneol
Atividade antimicrobiana
Terpenos
Ésteres do borneol
Leishmanicida
Antiproliferação celular e antiinflamatório
Micro-ondas
title_short Síntese e avaliação biológica de ésteres derivados do borneol 
title_full Síntese e avaliação biológica de ésteres derivados do borneol 
title_fullStr Síntese e avaliação biológica de ésteres derivados do borneol 
title_full_unstemmed Síntese e avaliação biológica de ésteres derivados do borneol 
title_sort Síntese e avaliação biológica de ésteres derivados do borneol 
author Aline Teixeira Maciel e Silva
author_facet Aline Teixeira Maciel e Silva
author_role author
dc.contributor.author.fl_str_mv Aline Teixeira Maciel e Silva
dc.subject.por.fl_str_mv Química Orgânica
Síntese orgânica
Produtos naturais
Esteres
topic Química Orgânica
Síntese orgânica
Produtos naturais
Esteres
Terpeno borneol
Atividade antimicrobiana
Terpenos
Ésteres do borneol
Leishmanicida
Antiproliferação celular e antiinflamatório
Micro-ondas
dc.subject.other.none.fl_str_mv Terpeno borneol
Atividade antimicrobiana
Terpenos
Ésteres do borneol
Leishmanicida
Antiproliferação celular e antiinflamatório
Micro-ondas
description The terpenes and its derivatives represent compounds of great interest to researchers because of the great potential as a source of new drugs. In this work, esters from the terpene borneol were synthesized using two methodologies (DIC/DMAP and SOCl2). It was also evaluated the microwave irradiation to obtain these compounds, without the use of solvent. It was synthesized 20 borneol esters, among them 18 are not described in the literature. Some of the reactions conducted under microwave irradiation and in the absence of solvent, led to products of rearrangement. The borneol esters had their structures elucidated through spectroscopic and spectrometric methods. The reaction condition in which were used DIC/DMAP and microwave irradiation, in less time produced better yields. The synthesized compounds were subjected to assays to evaluate its activity as antimicrobial, leishmanicidal, cellular antiproliferation and anti-inflammatory. The best results on the antimicrobial assays were found for bornyl 4-methoxybenzoate, bornyl 3,4-dimethoxybenzoate and bornyl 3,4,5-trimethoxybenzoate. It was not observed significative leishmanicidal effect produced by the borneol esters subjected to assay. In relation to the antiproliferative cells assays, bornyl octanoate, bornyl benzoate and bornyl 3,4,5-trimethoxybenzoate showed more promising results, with cytotoxic effects to cell lines of ovarian cancer (OVCAR-3), ovarian-resistant (NCI-ADR/RES), breast (MCF-7), bone marrow (K562) and kidney (786-0). In the anti-inflammatory assays, the bornyl hexanoate, bornyl octanoate, bornyl tetradecanoate, bornyl hexadecanoate, bornyl octadecanoate, bornyl benzoate, bornyl 3,5-dinitrobenzoate and bornyl nicotinate were those that provided better reduction in the edema induced by carrageenin.
publishDate 2014
dc.date.issued.fl_str_mv 2014-02-24
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2025-09-08T23:35:51Z
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