Estudo Fitoquímico das Folhas de Psychotria hoffmannseggiana Roem. & Schult (Rubiaceae)

Detalhes bibliográficos
Autor(a) principal: Naves, Raquel Ferreira
Data de Publicação: 2014
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UFG
Texto Completo: http://repositorio.bc.ufg.br/tede/handle/tede/3612
Resumo: Psychotria hoffmannseggiana (Wild. ex Roem. & Schult.) Müll. Arg. is a subshrub of the Rubiaceae family, which belongs to the genus Psychotria L. and to the subgenus Heteropsychotria. In this genus there is several indole alkaloids, recognized by their many bioactive properties. Furthermore, these alkaloids are used as chemotaxonomic markers in the classification and delimitation of the Psychotria genus. Up to this moment, no phytochemical study has been reported for the P. hoffmannseggiana species. Therefore, in the continuous searching for secondary metabolites, the crude ethanol extract (PHF-EB) from P. hoffmannseggiana leaves has been submitted to an acid-base fractionation, and the resultant fractions were subject to column chromatography. The methyl sinapate (PH-01) and the isoscopoletin (PH-02) were identified from the acid chloroform extract (PHFA-C). In the basic chloroform extract (PHFB-C), three indole alkaloids were isolated and identified: harman (PH-03), N-methyl-1,2,3,4-tetrahydro--carboline (PH-04), N-methyltryptamine (PH-05); as well as one polyindolic alkaloid, (+)chimonantine (PH-06). Besides, a great amount of monoterpenic indole alkaloid, the strictosidinic acid (PH-07), was isolated from the basic nbutanolic extract and ethyl acetate, PHFB-n-BuOH and PHFB-AcOEt, respectively. The -ethylglucose (PH-08) was isolated from the basic nbutanolic extract (PHFB-n-BuOH). The evaluation of the antioxidant activity of the extracts PHF-EB, PHFA-C, PHFB-C, PHFB-AcOEt and n-PHFB-nBuOH showed a 50% inhibition of DPPH radical at concentrations of 176,58 ± 1 35, 105.47 ± 0.88, 77.60 ± 0.36, 191.30 ± 0.68 and 271.96 ± 0.57 g.mL1, respectively.
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spelling Kato, Luciliahttp://lattes.cnpq.br/1362891438631386Kato, lucíliaSarragiotto, Maria HelenaFerri, Pedro Henriquehttp://lattes.cnpq.br/2330577601304742Naves, Raquel Ferreira2014-11-14T19:01:27Z2014-04-11NAVES, Raquel Ferreira. Estudo Fitoquímico das Folhas de Psychotria hoffmannseggiana Roem. & Schult (Rubiaceae). 2014. 212 f. Dissertação (Mestrado em Química) - Universidade Federal de Goiás, Goiânia, 2014.http://repositorio.bc.ufg.br/tede/handle/tede/3612Psychotria hoffmannseggiana (Wild. ex Roem. & Schult.) Müll. Arg. is a subshrub of the Rubiaceae family, which belongs to the genus Psychotria L. and to the subgenus Heteropsychotria. In this genus there is several indole alkaloids, recognized by their many bioactive properties. Furthermore, these alkaloids are used as chemotaxonomic markers in the classification and delimitation of the Psychotria genus. Up to this moment, no phytochemical study has been reported for the P. hoffmannseggiana species. Therefore, in the continuous searching for secondary metabolites, the crude ethanol extract (PHF-EB) from P. hoffmannseggiana leaves has been submitted to an acid-base fractionation, and the resultant fractions were subject to column chromatography. The methyl sinapate (PH-01) and the isoscopoletin (PH-02) were identified from the acid chloroform extract (PHFA-C). In the basic chloroform extract (PHFB-C), three indole alkaloids were isolated and identified: harman (PH-03), N-methyl-1,2,3,4-tetrahydro--carboline (PH-04), N-methyltryptamine (PH-05); as well as one polyindolic alkaloid, (+)chimonantine (PH-06). Besides, a great amount of monoterpenic indole alkaloid, the strictosidinic acid (PH-07), was isolated from the basic nbutanolic extract and ethyl acetate, PHFB-n-BuOH and PHFB-AcOEt, respectively. The -ethylglucose (PH-08) was isolated from the basic nbutanolic extract (PHFB-n-BuOH). The evaluation of the antioxidant activity of the extracts PHF-EB, PHFA-C, PHFB-C, PHFB-AcOEt and n-PHFB-nBuOH showed a 50% inhibition of DPPH radical at concentrations of 176,58 ± 1 35, 105.47 ± 0.88, 77.60 ± 0.36, 191.30 ± 0.68 and 271.96 ± 0.57 g.mL1, respectively.Psychotria hoffmannseggiana (Wild. ex Roem. & Schult.) Müll. Arg. é um subarbusto da família Rubiaceae, pertencente ao gênero Psychotria L. e ao subgênero Heteropsychotria. Nesse gênero há uma diversidade de alcaloides indólicos, conhecidos pelas diferentes propriedades bioativas. Além disso, esses alcaloides são usados como marcadores quimiotaxonômicos na classificação e delimitação do gênero Psychotria. Até o presente momento, nenhum estudo fitoquímico foi descrito para a espécie P. hoffmannseggiana. Portanto, na busca contínua dos metabólitos secundários, o extrato bruto etanólico das folhas da P. hoffmannseggiana (PHEt-EB) foi submetido a um fracionamento ácido-base e as frações resultantes foram submetidas a coluna cromatográfica. No extrato ácido clorofórmico (PHFA-C), identificou-se o sinapato de metila (PH-01) e a isoescopoletina (PH-02). No extrato básico clorofórmico (PHFB-C), foram isolados e identificados três alcaloides indólicos: harmano (PH-03), N-metil1,2,3,4-tetrahidro--carbolina (PH-04), N-metiltriptamina (PH-05) e um alcaloide polindólico, (+)-quimonantina (PH-06). Além desses, uma grande quantidade do alcaloide indólico monoterpênico, ácido estrictosidínico (PH07), foi isolado do extrato básico n-butanólico e acetato de etila, PHFB-nBuOH e PHFB-AcOEt, respectivamente. A -etilglicose (PH-08) foi isolada do extrato básico n-butanólico (PHFB-n-BuOH). A avaliação da atividade antioxidante dos extratos PHF-EB, PHFA-C, PHFB-C, PHFB-AcOEt e PHFBn-BuOH mostrou a inibição de 50% do radical DPPH nas concentrações de 176,58 ± 1,35, 105,47 ± 0,88, 77,60 ± 0,36, 191,30 ± 0,68 e 271,96 ± 0,57 g.mL-1, respectivamenteSubmitted by Marlene Santos (marlene.bc.ufg@gmail.com) on 2014-11-13T17:25:13Z No. of bitstreams: 2 Dissertação - Raquel Ferreira Naves - 2014.pdf: 4267508 bytes, checksum: bf2a0d1194ed1d13ea37554849f1df54 (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5)Approved for entry into archive by Jaqueline Silva (jtas29@gmail.com) on 2014-11-14T19:01:27Z (GMT) No. of bitstreams: 2 Dissertação - Raquel Ferreira Naves - 2014.pdf: 4267508 bytes, checksum: bf2a0d1194ed1d13ea37554849f1df54 (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5)Made available in DSpace on 2014-11-14T19:01:27Z (GMT). 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dc.title.por.fl_str_mv Estudo Fitoquímico das Folhas de Psychotria hoffmannseggiana Roem. & Schult (Rubiaceae)
dc.title.alternative.eng.fl_str_mv Phytochemical study on the leaves of the psychotria hoffmannseggiana roem. & schult (rubiaceae)
title Estudo Fitoquímico das Folhas de Psychotria hoffmannseggiana Roem. & Schult (Rubiaceae)
spellingShingle Estudo Fitoquímico das Folhas de Psychotria hoffmannseggiana Roem. & Schult (Rubiaceae)
Naves, Raquel Ferreira
Estudo fitoquímico
Psychotria hoffmannseggiana
Alcalóide
Phytochemical studies
Alkaloid
QUIMICA::FISICO-QUIMICA
title_short Estudo Fitoquímico das Folhas de Psychotria hoffmannseggiana Roem. & Schult (Rubiaceae)
title_full Estudo Fitoquímico das Folhas de Psychotria hoffmannseggiana Roem. & Schult (Rubiaceae)
title_fullStr Estudo Fitoquímico das Folhas de Psychotria hoffmannseggiana Roem. & Schult (Rubiaceae)
title_full_unstemmed Estudo Fitoquímico das Folhas de Psychotria hoffmannseggiana Roem. & Schult (Rubiaceae)
title_sort Estudo Fitoquímico das Folhas de Psychotria hoffmannseggiana Roem. & Schult (Rubiaceae)
author Naves, Raquel Ferreira
author_facet Naves, Raquel Ferreira
author_role author
dc.contributor.advisor1.fl_str_mv Kato, Lucilia
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/1362891438631386
dc.contributor.referee1.fl_str_mv Kato, lucília
dc.contributor.referee2.fl_str_mv Sarragiotto, Maria Helena
dc.contributor.referee3.fl_str_mv Ferri, Pedro Henrique
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/2330577601304742
dc.contributor.author.fl_str_mv Naves, Raquel Ferreira
contributor_str_mv Kato, Lucilia
Kato, lucília
Sarragiotto, Maria Helena
Ferri, Pedro Henrique
dc.subject.por.fl_str_mv Estudo fitoquímico
Psychotria hoffmannseggiana
Alcalóide
topic Estudo fitoquímico
Psychotria hoffmannseggiana
Alcalóide
Phytochemical studies
Alkaloid
QUIMICA::FISICO-QUIMICA
dc.subject.eng.fl_str_mv Phytochemical studies
Alkaloid
dc.subject.cnpq.fl_str_mv QUIMICA::FISICO-QUIMICA
description Psychotria hoffmannseggiana (Wild. ex Roem. & Schult.) Müll. Arg. is a subshrub of the Rubiaceae family, which belongs to the genus Psychotria L. and to the subgenus Heteropsychotria. In this genus there is several indole alkaloids, recognized by their many bioactive properties. Furthermore, these alkaloids are used as chemotaxonomic markers in the classification and delimitation of the Psychotria genus. Up to this moment, no phytochemical study has been reported for the P. hoffmannseggiana species. Therefore, in the continuous searching for secondary metabolites, the crude ethanol extract (PHF-EB) from P. hoffmannseggiana leaves has been submitted to an acid-base fractionation, and the resultant fractions were subject to column chromatography. The methyl sinapate (PH-01) and the isoscopoletin (PH-02) were identified from the acid chloroform extract (PHFA-C). In the basic chloroform extract (PHFB-C), three indole alkaloids were isolated and identified: harman (PH-03), N-methyl-1,2,3,4-tetrahydro--carboline (PH-04), N-methyltryptamine (PH-05); as well as one polyindolic alkaloid, (+)chimonantine (PH-06). Besides, a great amount of monoterpenic indole alkaloid, the strictosidinic acid (PH-07), was isolated from the basic nbutanolic extract and ethyl acetate, PHFB-n-BuOH and PHFB-AcOEt, respectively. The -ethylglucose (PH-08) was isolated from the basic nbutanolic extract (PHFB-n-BuOH). The evaluation of the antioxidant activity of the extracts PHF-EB, PHFA-C, PHFB-C, PHFB-AcOEt and n-PHFB-nBuOH showed a 50% inhibition of DPPH radical at concentrations of 176,58 ± 1 35, 105.47 ± 0.88, 77.60 ± 0.36, 191.30 ± 0.68 and 271.96 ± 0.57 g.mL1, respectively.
publishDate 2014
dc.date.accessioned.fl_str_mv 2014-11-14T19:01:27Z
dc.date.issued.fl_str_mv 2014-04-11
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.citation.fl_str_mv NAVES, Raquel Ferreira. Estudo Fitoquímico das Folhas de Psychotria hoffmannseggiana Roem. & Schult (Rubiaceae). 2014. 212 f. Dissertação (Mestrado em Química) - Universidade Federal de Goiás, Goiânia, 2014.
dc.identifier.uri.fl_str_mv http://repositorio.bc.ufg.br/tede/handle/tede/3612
identifier_str_mv NAVES, Raquel Ferreira. Estudo Fitoquímico das Folhas de Psychotria hoffmannseggiana Roem. & Schult (Rubiaceae). 2014. 212 f. Dissertação (Mestrado em Química) - Universidade Federal de Goiás, Goiânia, 2014.
url http://repositorio.bc.ufg.br/tede/handle/tede/3612
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language por
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dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Instituto de Química - IQ (RG)
publisher.none.fl_str_mv Universidade Federal de Goiás
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repository.name.fl_str_mv Repositório Institucional da UFG - Universidade Federal de Goiás (UFG)
repository.mail.fl_str_mv tasesdissertacoes.bc@ufg.br
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