Investigação de metabólitos secundários de Tabernaemontana catharinensis A. DC. – (Apocynaceae) e suas potenciais atividades antimicrobianas

Detalhes bibliográficos
Autor(a) principal: Reis, Frederico Luiz
Data de Publicação: 2018
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
dARK ID: ark:/26339/001300000vqxz
Texto Completo: http://repositorio.ufsm.br/handle/1/14945
Resumo: The phytochemical investigation of hexane and methanolic crude extracts and their fractions from the bark of the stem of Tabernaemontana catharinensis (Apocynaceae, commonly known as cobrina) led to the isolation of nine monoterpene indole alkaloids, voachalotin, affinisine, 16-epiaffinisin, voacangin, voacristin, vinpocetine, voacangine hydroxylindolenine, 12-methoxy-N4-methyl voachalotine and 12-methoxy-N4-methyl-5-epiquachalotine. The alkaloid vinpocetine and 12- methoxy-N4-methyl-5-epi voachalotin are isolated for the first time in the family Apocynaceae. A Nmethyl affinisine derivative was obtained through an affinisin methylation reaction. The extracts, fractions and isolated compounds showed antibacterial activity (Gram-positive and Gram-negative) and effective antifungal, against the tested strains. The inhibitory potential of the pairs of diastereoisomers, corinantean skeleton, affinisine, 16-epiaffinisina and 12-methoxy-N4-methyl-5- epivoachalotine, 12-methoxy-N4-methyl voachalotine presented MIC values (1.56 μg.mL -1) lower than the fluconazole standard (MIC 3.12 μg.mL-1) compared to fungal strains. The methylation of the affinisine compound potentiated the inhibition against some microorganisms. The ibogan skeletal alkaloids, Voacangina, and Voacristina presented better inhibitory potentials against bacteria, presenting MIC of 3.12; 12.5 and 25 μg.mL -1 against the microorganisms Pseudomonas aeroginosa, Bacillus cereus and Salmonella typhimurium, respectively, being equal to or close to the chloramphenicol standard. The importance of stereochemistry in relation to the effectiveness of the MIC, which is visible in the activities presented in this paper. Thus, the phytochemical study and the pharmacological activities of the identified compounds of the stem bark of T.catharinensis broaden the knowledge alluding to chemotaxonomy, as well as justifying its antifungal use in folk medicine.
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spelling Investigação de metabólitos secundários de Tabernaemontana catharinensis A. DC. – (Apocynaceae) e suas potenciais atividades antimicrobianasResearch of secondary metabolites of Tabernaemontana catharinensis A. DC. - (Apocynaceae) and its potential antimicrobial activitiesTabernaemontana catharinensisAlcaloide indólicoVinpocetinaAtividade antimicrobianaIndole alkaloidVinpocetineAntimicrobian activityCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICAThe phytochemical investigation of hexane and methanolic crude extracts and their fractions from the bark of the stem of Tabernaemontana catharinensis (Apocynaceae, commonly known as cobrina) led to the isolation of nine monoterpene indole alkaloids, voachalotin, affinisine, 16-epiaffinisin, voacangin, voacristin, vinpocetine, voacangine hydroxylindolenine, 12-methoxy-N4-methyl voachalotine and 12-methoxy-N4-methyl-5-epiquachalotine. The alkaloid vinpocetine and 12- methoxy-N4-methyl-5-epi voachalotin are isolated for the first time in the family Apocynaceae. A Nmethyl affinisine derivative was obtained through an affinisin methylation reaction. The extracts, fractions and isolated compounds showed antibacterial activity (Gram-positive and Gram-negative) and effective antifungal, against the tested strains. The inhibitory potential of the pairs of diastereoisomers, corinantean skeleton, affinisine, 16-epiaffinisina and 12-methoxy-N4-methyl-5- epivoachalotine, 12-methoxy-N4-methyl voachalotine presented MIC values (1.56 μg.mL -1) lower than the fluconazole standard (MIC 3.12 μg.mL-1) compared to fungal strains. The methylation of the affinisine compound potentiated the inhibition against some microorganisms. The ibogan skeletal alkaloids, Voacangina, and Voacristina presented better inhibitory potentials against bacteria, presenting MIC of 3.12; 12.5 and 25 μg.mL -1 against the microorganisms Pseudomonas aeroginosa, Bacillus cereus and Salmonella typhimurium, respectively, being equal to or close to the chloramphenicol standard. The importance of stereochemistry in relation to the effectiveness of the MIC, which is visible in the activities presented in this paper. Thus, the phytochemical study and the pharmacological activities of the identified compounds of the stem bark of T.catharinensis broaden the knowledge alluding to chemotaxonomy, as well as justifying its antifungal use in folk medicine.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESA investigação fitoquímica dos extratos brutos hexânico e metanólico e suas frações, oriundas da casca do caule de Tabernaemontana catharinensis (Apocynaceae, conhecida popularmente como cobrina), levou ao isolamento de nove alcaloides indólicos monoterpênicos, voachalotina, affinisina, 16- epiaffinisina, voacangina, voacristina, vinpocetina, voacangina hidroxi-indolenina, 12-metoxi-N4- metil voachalotina e 12-metoxi-N4-metil-5-epi voachalotina. O alcaloide vinpocetina e 12-metoxi-N4- metil- 5-epi voachalotina são isolados pela primeira vez na família Apocynaceae. Através de uma reação de metilação de affinisina foi obtido o derivado N4-metil affinisina. Os extratos, frações e compostos isolados apresentaram atividade antibacteriana (Gram-positivas e Gram-negativas) e antifúngica efetivas, contra as cepas testadas. O potencial inibitório dos pares de diasteroisômeros, de esqueleto corinanteano, affinisina, 16-epiaffinisina e 12-metoxi-N4-metil-5-epivoachalotina, 12- metoxi-N4-metil voachalotina, apresentaram valores de CIM (1,56 μg.mL-1) menores que o padrão fluconazol (CIM 3,12 μg.mL-1), frente a cepas de fungos. A metilação do composto affinisina potencializou a inibição frente a alguns micro-organismos. Os alcaloides de esqueleto ibogano, Voacangina, Voacristina apresentaram melhores potenciais inibitórios frente a bactérias, apresentando CIM de 3,12; 12,5 e 25 μg.mL-1 frente aos micro-organismos Pseudomonas aeroginosa, Bacillus cereus e Salmonella typhimurium, respectivamente, sendo igual ou próximo ao padrão cloranfenicol. A importância da estereoquímica em relação à efetividade da CIM, o que é visível nas atividades apresentadas neste trabalho. Dessa forma, o estudo fitoquímico e das atividades farmacológicas dos compostos identificados da casca do caule de T.catharinensis amplia os conhecimentos alusivos à quimiotaxonomia, bem como justifica seu uso antifúngico na medicina popular.Universidade Federal de Santa MariaBrasilQuímicaUFSMPrograma de Pós-Graduação em QuímicaCentro de Ciências Naturais e ExatasMostardeiro, Marco Aureliohttp://lattes.cnpq.br/6195396264565980Dalcol, Ionara Irionhttp://lattes.cnpq.br/9769548819312192Ilha, Viniciushttp://lattes.cnpq.br/3882671719676564Reis, Frederico Luiz2018-11-27T10:41:03Z2018-11-27T10:41:03Z2018-07-17info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/14945ark:/26339/001300000vqxzporAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2018-11-28T05:01:36Zoai:repositorio.ufsm.br:1/14945Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2018-11-28T05:01:36Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Investigação de metabólitos secundários de Tabernaemontana catharinensis A. DC. – (Apocynaceae) e suas potenciais atividades antimicrobianas
Research of secondary metabolites of Tabernaemontana catharinensis A. DC. - (Apocynaceae) and its potential antimicrobial activities
title Investigação de metabólitos secundários de Tabernaemontana catharinensis A. DC. – (Apocynaceae) e suas potenciais atividades antimicrobianas
spellingShingle Investigação de metabólitos secundários de Tabernaemontana catharinensis A. DC. – (Apocynaceae) e suas potenciais atividades antimicrobianas
Reis, Frederico Luiz
Tabernaemontana catharinensis
Alcaloide indólico
Vinpocetina
Atividade antimicrobiana
Indole alkaloid
Vinpocetine
Antimicrobian activity
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Investigação de metabólitos secundários de Tabernaemontana catharinensis A. DC. – (Apocynaceae) e suas potenciais atividades antimicrobianas
title_full Investigação de metabólitos secundários de Tabernaemontana catharinensis A. DC. – (Apocynaceae) e suas potenciais atividades antimicrobianas
title_fullStr Investigação de metabólitos secundários de Tabernaemontana catharinensis A. DC. – (Apocynaceae) e suas potenciais atividades antimicrobianas
title_full_unstemmed Investigação de metabólitos secundários de Tabernaemontana catharinensis A. DC. – (Apocynaceae) e suas potenciais atividades antimicrobianas
title_sort Investigação de metabólitos secundários de Tabernaemontana catharinensis A. DC. – (Apocynaceae) e suas potenciais atividades antimicrobianas
author Reis, Frederico Luiz
author_facet Reis, Frederico Luiz
author_role author
dc.contributor.none.fl_str_mv Mostardeiro, Marco Aurelio
http://lattes.cnpq.br/6195396264565980
Dalcol, Ionara Irion
http://lattes.cnpq.br/9769548819312192
Ilha, Vinicius
http://lattes.cnpq.br/3882671719676564
dc.contributor.author.fl_str_mv Reis, Frederico Luiz
dc.subject.por.fl_str_mv Tabernaemontana catharinensis
Alcaloide indólico
Vinpocetina
Atividade antimicrobiana
Indole alkaloid
Vinpocetine
Antimicrobian activity
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
topic Tabernaemontana catharinensis
Alcaloide indólico
Vinpocetina
Atividade antimicrobiana
Indole alkaloid
Vinpocetine
Antimicrobian activity
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description The phytochemical investigation of hexane and methanolic crude extracts and their fractions from the bark of the stem of Tabernaemontana catharinensis (Apocynaceae, commonly known as cobrina) led to the isolation of nine monoterpene indole alkaloids, voachalotin, affinisine, 16-epiaffinisin, voacangin, voacristin, vinpocetine, voacangine hydroxylindolenine, 12-methoxy-N4-methyl voachalotine and 12-methoxy-N4-methyl-5-epiquachalotine. The alkaloid vinpocetine and 12- methoxy-N4-methyl-5-epi voachalotin are isolated for the first time in the family Apocynaceae. A Nmethyl affinisine derivative was obtained through an affinisin methylation reaction. The extracts, fractions and isolated compounds showed antibacterial activity (Gram-positive and Gram-negative) and effective antifungal, against the tested strains. The inhibitory potential of the pairs of diastereoisomers, corinantean skeleton, affinisine, 16-epiaffinisina and 12-methoxy-N4-methyl-5- epivoachalotine, 12-methoxy-N4-methyl voachalotine presented MIC values (1.56 μg.mL -1) lower than the fluconazole standard (MIC 3.12 μg.mL-1) compared to fungal strains. The methylation of the affinisine compound potentiated the inhibition against some microorganisms. The ibogan skeletal alkaloids, Voacangina, and Voacristina presented better inhibitory potentials against bacteria, presenting MIC of 3.12; 12.5 and 25 μg.mL -1 against the microorganisms Pseudomonas aeroginosa, Bacillus cereus and Salmonella typhimurium, respectively, being equal to or close to the chloramphenicol standard. The importance of stereochemistry in relation to the effectiveness of the MIC, which is visible in the activities presented in this paper. Thus, the phytochemical study and the pharmacological activities of the identified compounds of the stem bark of T.catharinensis broaden the knowledge alluding to chemotaxonomy, as well as justifying its antifungal use in folk medicine.
publishDate 2018
dc.date.none.fl_str_mv 2018-11-27T10:41:03Z
2018-11-27T10:41:03Z
2018-07-17
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://repositorio.ufsm.br/handle/1/14945
dc.identifier.dark.fl_str_mv ark:/26339/001300000vqxz
url http://repositorio.ufsm.br/handle/1/14945
identifier_str_mv ark:/26339/001300000vqxz
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Química
UFSM
Programa de Pós-Graduação em Química
Centro de Ciências Naturais e Exatas
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Química
UFSM
Programa de Pós-Graduação em Química
Centro de Ciências Naturais e Exatas
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da UFSM
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Manancial - Repositório Digital da UFSM
collection Manancial - Repositório Digital da UFSM
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com
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