Estudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendula

Detalhes bibliográficos
Ano de defesa: 2018
Autor(a) principal: Monteiro, Jackelyne Alves
Orientador(a): Silva, Maria Goretti de Vasconcelos
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Não Informado pela instituição
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: http://www.repositorio.ufc.br/handle/riufc/60431
Resumo: The knowledge of the chemical composition of higher plants has been the main objective of the study of the chemistry of natural products, since vast amount of botanical species remains without any chemical or pharmacological study, which makes difficult the rational use of botanical biodiversity. An important application of this use is the discovery of compounds from natural sources, potentially candidates for new drugs. This work reports the chemical and pharmacological study of two native species of the Northeastern flora, Senna cana I & B and Senna pendula I & B. The steps of the development of the work include tha dereplication by HPLC-DAD, the isolation and identification of substances from extracts of S. pendula, a proposal of methodology for optimization of the extraction of flavonoids, applied here, to S. fistula and S. obtusifolia, and the in silico study of the antimalarial potential of anthraquinones and flavonoids of Senna spp. The analysis of the results allowed the identification of 13 flavonoids in the two species studied, which were afterward quantified by HPLC-IES-MS. The chromatographic treatment of the hexane and ethanolic extracts of S. pendula made possible the isolation and identification of three triterpenes: frideline, α and β-amirin, and two flavonoids, epicatechin and quercetin. Structural elucidation was performed using spectroscopic techniques such as MS and NMR H1, C13 mono and bi-dimensional (HSQC). The biopharmacological potential of these species were also investigated by antioxidant activity, total phenolic and flavonoid content, anticholinesterase activity, larvicide against Aedes aegypti, toxicity against Artemia saline and inhibition of the angiotensin I converting enzyme (ACE). All reported substances are being registered for the first time in the species Senna cana and Senna pendula.
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spelling Monteiro, Jackelyne AlvesSilva, Maria Goretti de Vasconcelos2021-09-13T17:09:22Z2021-09-13T17:09:22Z2018MONTEIRO, Jackelyne Alves. Estudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendula. 2018. 244 f. Tese (Doutorado em Química Orgânica) - Universidade Federal do Ceará, Fortaleza, 2018.http://www.repositorio.ufc.br/handle/riufc/60431The knowledge of the chemical composition of higher plants has been the main objective of the study of the chemistry of natural products, since vast amount of botanical species remains without any chemical or pharmacological study, which makes difficult the rational use of botanical biodiversity. An important application of this use is the discovery of compounds from natural sources, potentially candidates for new drugs. This work reports the chemical and pharmacological study of two native species of the Northeastern flora, Senna cana I & B and Senna pendula I & B. The steps of the development of the work include tha dereplication by HPLC-DAD, the isolation and identification of substances from extracts of S. pendula, a proposal of methodology for optimization of the extraction of flavonoids, applied here, to S. fistula and S. obtusifolia, and the in silico study of the antimalarial potential of anthraquinones and flavonoids of Senna spp. The analysis of the results allowed the identification of 13 flavonoids in the two species studied, which were afterward quantified by HPLC-IES-MS. The chromatographic treatment of the hexane and ethanolic extracts of S. pendula made possible the isolation and identification of three triterpenes: frideline, α and β-amirin, and two flavonoids, epicatechin and quercetin. Structural elucidation was performed using spectroscopic techniques such as MS and NMR H1, C13 mono and bi-dimensional (HSQC). The biopharmacological potential of these species were also investigated by antioxidant activity, total phenolic and flavonoid content, anticholinesterase activity, larvicide against Aedes aegypti, toxicity against Artemia saline and inhibition of the angiotensin I converting enzyme (ACE). All reported substances are being registered for the first time in the species Senna cana and Senna pendula.O conhecimento da composição química de plantas superiores tem sido o objetivo principal de estudo da química de produtos naturais, pois vasta quantidade de espécies botânicas permanece sem qualquer estudo químico ou farmacológico, dificultando assim, o aproveitamento racional da biodiversidade botânica. Uma aplicação importante deste aproveitamento está na descoberta de compostos de fontes naturais, potencialmente candidatos a novos fármacos. Este trabalho relata o estudo químico e farmacológico de duas espécies nativas da flora nordestina, Senna cana I & B e Senna pendula I & B. As etapas compreendidas no desenvolvimento do trabalho incluem a desreplicação por CLAE-DAD, o isolamento e identificação de substâncias dos extratos hexânicos e etanólico de S. pendula, uma proposta de metodologia para otimização da extração de flavonoides, aplicada a S. fistula e S. obtusifolia, e o estudo in silico do potencial antimalárico de antraquinonas e flavonoides de Senna spp. A análise dos resultados possibilitou a identificação de 13 flavonoides nas duas espécies estudadas, que foram posteriormente quantificados por CLAE-IES-EM. O tratamento cromatográfico dos extratos hexânico e etanólico de S. pendula, possibilitou o isolamento e identificação de três triterpenos: fridelina, α e β-amirina, e dois flavonoides, a epicatequina e a quercetina. A elucidação estrutural foi realizada através de técnicas espectroscópicas como: ressonância magnética nuclear de hidrogênio-1 e carbono-13, mono e bidimensional do tipo HSQC. Os potenciais farmacológicos destas espécies também foram investigados, através dos ensaios de atividade antioxidante, teor de fenólicos e flavonoides totais, atividades anticolinesterásica, larvicida frente a Aedes aegpti, toxicidade frente a Artemia salina e inibição da enzima conversora da angiotensina I. Todas as substâncias isoladas e identificadas estão sendo relatadas pela primeira vez nas espécies Senna cana e Senna pendula.SennaAntioxidanteFlavonoideInsilicoEstudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendulaChemical and pharmacological study in vitro and in silico of Senna spp. native of the northeast: Senna cana and Senna pendulainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisporreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccessLICENSElicense.txtlicense.txttext/plain; charset=utf-81748http://repositorio.ufc.br/bitstream/riufc/60431/2/license.txt8a4605be74aa9ea9d79846c1fba20a33MD52ORIGINAL2018_tese_jamonteiro.pdf2018_tese_jamonteiro.pdfapplication/pdf10152096http://repositorio.ufc.br/bitstream/riufc/60431/3/2018_tese_jamonteiro.pdf906f5c53e110c0f46ef630b796d2060bMD53riufc/604312021-10-06 11:37:22.593oai:repositorio.ufc.br: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Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2021-10-06T14:37:22Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.pt_BR.fl_str_mv Estudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendula
dc.title.en.pt_BR.fl_str_mv Chemical and pharmacological study in vitro and in silico of Senna spp. native of the northeast: Senna cana and Senna pendula
title Estudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendula
spellingShingle Estudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendula
Monteiro, Jackelyne Alves
Senna
Antioxidante
Flavonoide
Insilico
title_short Estudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendula
title_full Estudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendula
title_fullStr Estudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendula
title_full_unstemmed Estudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendula
title_sort Estudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendula
author Monteiro, Jackelyne Alves
author_facet Monteiro, Jackelyne Alves
author_role author
dc.contributor.author.fl_str_mv Monteiro, Jackelyne Alves
dc.contributor.advisor1.fl_str_mv Silva, Maria Goretti de Vasconcelos
contributor_str_mv Silva, Maria Goretti de Vasconcelos
dc.subject.por.fl_str_mv Senna
Antioxidante
Flavonoide
Insilico
topic Senna
Antioxidante
Flavonoide
Insilico
description The knowledge of the chemical composition of higher plants has been the main objective of the study of the chemistry of natural products, since vast amount of botanical species remains without any chemical or pharmacological study, which makes difficult the rational use of botanical biodiversity. An important application of this use is the discovery of compounds from natural sources, potentially candidates for new drugs. This work reports the chemical and pharmacological study of two native species of the Northeastern flora, Senna cana I & B and Senna pendula I & B. The steps of the development of the work include tha dereplication by HPLC-DAD, the isolation and identification of substances from extracts of S. pendula, a proposal of methodology for optimization of the extraction of flavonoids, applied here, to S. fistula and S. obtusifolia, and the in silico study of the antimalarial potential of anthraquinones and flavonoids of Senna spp. The analysis of the results allowed the identification of 13 flavonoids in the two species studied, which were afterward quantified by HPLC-IES-MS. The chromatographic treatment of the hexane and ethanolic extracts of S. pendula made possible the isolation and identification of three triterpenes: frideline, α and β-amirin, and two flavonoids, epicatechin and quercetin. Structural elucidation was performed using spectroscopic techniques such as MS and NMR H1, C13 mono and bi-dimensional (HSQC). The biopharmacological potential of these species were also investigated by antioxidant activity, total phenolic and flavonoid content, anticholinesterase activity, larvicide against Aedes aegypti, toxicity against Artemia saline and inhibition of the angiotensin I converting enzyme (ACE). All reported substances are being registered for the first time in the species Senna cana and Senna pendula.
publishDate 2018
dc.date.issued.fl_str_mv 2018
dc.date.accessioned.fl_str_mv 2021-09-13T17:09:22Z
dc.date.available.fl_str_mv 2021-09-13T17:09:22Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.citation.fl_str_mv MONTEIRO, Jackelyne Alves. Estudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendula. 2018. 244 f. Tese (Doutorado em Química Orgânica) - Universidade Federal do Ceará, Fortaleza, 2018.
dc.identifier.uri.fl_str_mv http://www.repositorio.ufc.br/handle/riufc/60431
identifier_str_mv MONTEIRO, Jackelyne Alves. Estudo químico e farmacológico in vitro e in silico de Senna Spp. Nativas do nordeste: Senna cana e Senna pendula. 2018. 244 f. Tese (Doutorado em Química Orgânica) - Universidade Federal do Ceará, Fortaleza, 2018.
url http://www.repositorio.ufc.br/handle/riufc/60431
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