Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicos

Detalhes bibliográficos
Autor(a) principal: Silva, Luiz André de Araújo
Data de Publicação: 2016
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Biblioteca Digital de Teses e Dissertações da UFPB
Texto Completo: https://repositorio.ufpb.br/jspui/handle/tede/9080
Resumo: Alkaloids are secondary metabolites of great medical importance, covering a diverse group of nitrogen containing molecules in its structure, the number of alkaloid containing the tetrahidroisoquinolínico skeleton 1-substituted is extensive and impressive pharmacological versatility of this class arouses interest in experimental pharmacologists, the importance. This work has as objective, the synthesis of tetrahydroisoquinolines and provide material for future pharmacological studies both in-vivo and in-vitro. For the synthesis of phenyltetrahydroisoquinolinics alkaloids, benzyltetrahydroisoquinilinic and phenyltetrahydro-β-carboline the Pictet-Spengler reaction was aplicated. With the aim of expanding the pharmacological studies of the alkaloid (1-(3-dimethoxy-4-hydroxyphenyl)-7-methoxy-1,2,3,4,-tetrahydroisoquinoline (MTHP) your synthesis was repeated. 4 alkaloids were obtained, 2 phenyltetrahydroisoquinolinic (1-(3,5-dimethoxy-4-hydroxyphenyl)-7-methoxy-1,2,3,4-tetrahydroisoquinoline (73%) and 1-(2-hydroxyphenyl)-7-methoxy-1,2,3,4-tetrahydroisoquinoline (54%)), 1 phenyltetrahydro-β-carboline (1-(3,5-dimethoxy-4-hydroxyphenyl)-1,2,3,4,-tetrahydro-β-carboline (38%)) and 1 benzyltetrhydroisoquinilínic (1-(1-ethyl-3,4-metilenodioxidofenil)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline (87%)). From the material available for the pharmacological MTHP tests showed low toxicity without genotoxicity, its immunomodulatory mechanism in asthma is related to regulation of TH2 profile.
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spelling Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicosTetrahidroisoquinolínicosPictet-SpenglerAlcaloidesTetrahydroisoquinolinePictet-SpenglerAlkaloidsCIENCIAS BIOLOGICAS::FARMACOLOGIAAlkaloids are secondary metabolites of great medical importance, covering a diverse group of nitrogen containing molecules in its structure, the number of alkaloid containing the tetrahidroisoquinolínico skeleton 1-substituted is extensive and impressive pharmacological versatility of this class arouses interest in experimental pharmacologists, the importance. This work has as objective, the synthesis of tetrahydroisoquinolines and provide material for future pharmacological studies both in-vivo and in-vitro. For the synthesis of phenyltetrahydroisoquinolinics alkaloids, benzyltetrahydroisoquinilinic and phenyltetrahydro-β-carboline the Pictet-Spengler reaction was aplicated. With the aim of expanding the pharmacological studies of the alkaloid (1-(3-dimethoxy-4-hydroxyphenyl)-7-methoxy-1,2,3,4,-tetrahydroisoquinoline (MTHP) your synthesis was repeated. 4 alkaloids were obtained, 2 phenyltetrahydroisoquinolinic (1-(3,5-dimethoxy-4-hydroxyphenyl)-7-methoxy-1,2,3,4-tetrahydroisoquinoline (73%) and 1-(2-hydroxyphenyl)-7-methoxy-1,2,3,4-tetrahydroisoquinoline (54%)), 1 phenyltetrahydro-β-carboline (1-(3,5-dimethoxy-4-hydroxyphenyl)-1,2,3,4,-tetrahydro-β-carboline (38%)) and 1 benzyltetrhydroisoquinilínic (1-(1-ethyl-3,4-metilenodioxidofenil)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline (87%)). From the material available for the pharmacological MTHP tests showed low toxicity without genotoxicity, its immunomodulatory mechanism in asthma is related to regulation of TH2 profile.Alcaloides são metabólitos secundários de grande importância medicinal, abrangendo um grupo diverso de moléculas contendo nitrogênio na sua estrutura. O número de alcaloides que contém o esqueleto tetrahidroisoquinolínico 1-substituído é extenso e a impressionante versatilidade farmacológica desta classe desperta o interesse nos farmacologistas experimentais. Visto a importância dos alcaloides isoquinolínicos, o nosso trabalho tem como objetivo a síntese de derivados tetrahidroisoquinolínicos e fornecer material para futuros estudos farmacológicos tanto in-vivo como in-vitro. Para a síntese dos alcaloides feniltetrahidroisoquinolínicos, benziltratrahidroisoquinilínicos e feniltetrahidro-β-carbolínicos foi utilizado a reação de Pictet-Spengler. Com o objetivo de ampliar os estudos farmacológicos a respeito do alcaloide (1-(3-dimetoxi-4-hidroxifenil)-7-metoxi-1,2,3,4,-tetrahidro isoquinolina (MTHP) refizemos a sua síntese como descrito na literatura. Obtivemos 4 alcaloides, sendo 2 deles feniltetrahidroisoquinolínicos (1-(3,5-dimetoxi-4-hidroxifenil)-7-metoxi-1,2,3,4,-tetrahidro isoquinolina (73%) e 1-(2-hidroxifenil)-7-metoxi-1,2,3,4,-tetrahidro isoquinolina (54%)), 1 feniltetrahidro-β-carbolínicos (1-(3,5-dimetoxi-4-hidroxifenil)-1,2,3,4,-tetrahidro-β-carbolina (38%)) e 1 benziltratrahidroisoquinilínicos (1-(1-etil-3,4-metilenodioxidofenil)-6,7-dimetoxi-1,2,3,4,-tetrahidro isoquinolina(87%)). A partir da disponibilização de material para os testes farmacológicos do MTHP, apresentou baixa toxicidade sem genotoxicidade, seu mecanismo imunomodulador na asma está relacionado a regulação do perfil TH2.Universidade Federal da ParaíbaBrasilFarmacologiaPrograma de Pós-Graduação em Produtos Naturais e Sintéticos BioativosUFPBOliveira, Eduardo de Jesushttp://lattes.cnpq.br/1293090609428232Silva, Luiz André de Araújo2017-07-10T13:59:53Z2018-07-21T00:25:54Z2018-07-21T00:25:54Z2016-05-27info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfSILVA, Luiz André de Araújo. Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicos. 2016. 82 f. Dissertação (Mestrado em Produtos Naturais e Sintéticos Bioativos) - Universidade Federal da Paraíba, João Pessoa, 2016.https://repositorio.ufpb.br/jspui/handle/tede/9080porinfo:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UFPBinstname:Universidade Federal da Paraíba (UFPB)instacron:UFPB2018-09-06T02:27:36Zoai:repositorio.ufpb.br:tede/9080Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufpb.br/PUBhttp://tede.biblioteca.ufpb.br:8080/oai/requestdiretoria@ufpb.br|| diretoria@ufpb.bropendoar:2018-09-06T02:27:36Biblioteca Digital de Teses e Dissertações da UFPB - Universidade Federal da Paraíba (UFPB)false
dc.title.none.fl_str_mv Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicos
title Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicos
spellingShingle Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicos
Silva, Luiz André de Araújo
Tetrahidroisoquinolínicos
Pictet-Spengler
Alcaloides
Tetrahydroisoquinoline
Pictet-Spengler
Alkaloids
CIENCIAS BIOLOGICAS::FARMACOLOGIA
title_short Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicos
title_full Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicos
title_fullStr Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicos
title_full_unstemmed Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicos
title_sort Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicos
author Silva, Luiz André de Araújo
author_facet Silva, Luiz André de Araújo
author_role author
dc.contributor.none.fl_str_mv Oliveira, Eduardo de Jesus
http://lattes.cnpq.br/1293090609428232
dc.contributor.author.fl_str_mv Silva, Luiz André de Araújo
dc.subject.por.fl_str_mv Tetrahidroisoquinolínicos
Pictet-Spengler
Alcaloides
Tetrahydroisoquinoline
Pictet-Spengler
Alkaloids
CIENCIAS BIOLOGICAS::FARMACOLOGIA
topic Tetrahidroisoquinolínicos
Pictet-Spengler
Alcaloides
Tetrahydroisoquinoline
Pictet-Spengler
Alkaloids
CIENCIAS BIOLOGICAS::FARMACOLOGIA
description Alkaloids are secondary metabolites of great medical importance, covering a diverse group of nitrogen containing molecules in its structure, the number of alkaloid containing the tetrahidroisoquinolínico skeleton 1-substituted is extensive and impressive pharmacological versatility of this class arouses interest in experimental pharmacologists, the importance. This work has as objective, the synthesis of tetrahydroisoquinolines and provide material for future pharmacological studies both in-vivo and in-vitro. For the synthesis of phenyltetrahydroisoquinolinics alkaloids, benzyltetrahydroisoquinilinic and phenyltetrahydro-β-carboline the Pictet-Spengler reaction was aplicated. With the aim of expanding the pharmacological studies of the alkaloid (1-(3-dimethoxy-4-hydroxyphenyl)-7-methoxy-1,2,3,4,-tetrahydroisoquinoline (MTHP) your synthesis was repeated. 4 alkaloids were obtained, 2 phenyltetrahydroisoquinolinic (1-(3,5-dimethoxy-4-hydroxyphenyl)-7-methoxy-1,2,3,4-tetrahydroisoquinoline (73%) and 1-(2-hydroxyphenyl)-7-methoxy-1,2,3,4-tetrahydroisoquinoline (54%)), 1 phenyltetrahydro-β-carboline (1-(3,5-dimethoxy-4-hydroxyphenyl)-1,2,3,4,-tetrahydro-β-carboline (38%)) and 1 benzyltetrhydroisoquinilínic (1-(1-ethyl-3,4-metilenodioxidofenil)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline (87%)). From the material available for the pharmacological MTHP tests showed low toxicity without genotoxicity, its immunomodulatory mechanism in asthma is related to regulation of TH2 profile.
publishDate 2016
dc.date.none.fl_str_mv 2016-05-27
2017-07-10T13:59:53Z
2018-07-21T00:25:54Z
2018-07-21T00:25:54Z
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 SILVA, Luiz André de Araújo. Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicos. 2016. 82 f. Dissertação (Mestrado em Produtos Naturais e Sintéticos Bioativos) - Universidade Federal da Paraíba, João Pessoa, 2016.
https://repositorio.ufpb.br/jspui/handle/tede/9080
identifier_str_mv SILVA, Luiz André de Araújo. Novos derivados sintéticos de alcaloides tetrahidroisoquinolínicos. 2016. 82 f. Dissertação (Mestrado em Produtos Naturais e Sintéticos Bioativos) - Universidade Federal da Paraíba, João Pessoa, 2016.
url https://repositorio.ufpb.br/jspui/handle/tede/9080
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 da Paraíba
Brasil
Farmacologia
Programa de Pós-Graduação em Produtos Naturais e Sintéticos Bioativos
UFPB
publisher.none.fl_str_mv Universidade Federal da Paraíba
Brasil
Farmacologia
Programa de Pós-Graduação em Produtos Naturais e Sintéticos Bioativos
UFPB
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações da UFPB
instname:Universidade Federal da Paraíba (UFPB)
instacron:UFPB
instname_str Universidade Federal da Paraíba (UFPB)
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reponame_str Biblioteca Digital de Teses e Dissertações da UFPB
collection Biblioteca Digital de Teses e Dissertações da UFPB
repository.name.fl_str_mv Biblioteca Digital de Teses e Dissertações da UFPB - Universidade Federal da Paraíba (UFPB)
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