Síntese e avaliação biológica de ésteres derivados do borneol 

Detalhes bibliográficos
Autor(a) principal: Aline Teixeira Maciel e Silva
Data de Publicação: 2014
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UFMG
Texto Completo: http://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.
id UFMG_f746eb765adffcdce536e0a98eaa79a3
oai_identifier_str oai:repositorio.ufmg.br:1843/SFSA-9JTSGH
network_acronym_str UFMG
network_name_str Repositório Institucional da UFMG
repository_id_str
spelling Síntese e avaliação biológica de ésteres derivados do borneol Terpeno borneolAtividade antimicrobianaTerpenosÉsteres do borneolLeishmanicidaAntiproliferação celular e antiinflamatórioMicro-ondasQuímica OrgânicaSíntese orgânicaProdutos naturaisEsteresThe 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.Os 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.Universidade Federal de Minas GeraisUFMGGracia Divina de Fatima SilvaRoqueline Rodrigues Silva de MirandaMarcelo Moreira BrittoHenriete da Silva VieiraAline Teixeira Maciel e Silva2019-08-10T16:40:40Z2019-08-10T16:40:40Z2014-02-24info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/1843/SFSA-9JTSGHinfo:eu-repo/semantics/openAccessporreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMG2019-11-14T09:31:22Zoai:repositorio.ufmg.br:1843/SFSA-9JTSGHRepositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2019-11-14T09:31:22Repositório 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
Terpeno borneol
Atividade antimicrobiana
Terpenos
Ésteres do borneol
Leishmanicida
Antiproliferação celular e antiinflamatório
Micro-ondas
Química Orgânica
Síntese orgânica
Produtos naturais
Esteres
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.none.fl_str_mv Gracia Divina de Fatima Silva
Roqueline Rodrigues Silva de Miranda
Marcelo Moreira Britto
Henriete da Silva Vieira
dc.contributor.author.fl_str_mv Aline Teixeira Maciel e Silva
dc.subject.por.fl_str_mv Terpeno borneol
Atividade antimicrobiana
Terpenos
Ésteres do borneol
Leishmanicida
Antiproliferação celular e antiinflamatório
Micro-ondas
Química Orgânica
Síntese orgânica
Produtos naturais
Esteres
topic Terpeno borneol
Atividade antimicrobiana
Terpenos
Ésteres do borneol
Leishmanicida
Antiproliferação celular e antiinflamatório
Micro-ondas
Química Orgânica
Síntese orgânica
Produtos naturais
Esteres
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.none.fl_str_mv 2014-02-24
2019-08-10T16:40:40Z
2019-08-10T16:40:40Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1843/SFSA-9JTSGH
url http://hdl.handle.net/1843/SFSA-9JTSGH
dc.language.iso.fl_str_mv por
language por
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 Universidade Federal de Minas Gerais
UFMG
publisher.none.fl_str_mv Universidade Federal de Minas Gerais
UFMG
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFMG
instname:Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
instname_str Universidade Federal de Minas Gerais (UFMG)
instacron_str UFMG
institution UFMG
reponame_str Repositório Institucional da UFMG
collection Repositório Institucional da UFMG
repository.name.fl_str_mv Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)
repository.mail.fl_str_mv repositorio@ufmg.br
_version_ 1823248237534904320