Flavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition.
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFOP |
Texto Completo: | http://www.repositorio.ufop.br/handle/123456789/8611 https://doi.org/10.1016/j.phytol.2016.10.024 |
Resumo: | Although Maytenus robusta aqueous infusions of leaves are used in Brazilian traditional medicine for stomach disease treatment, only a few chemical studies of this species are found in literature. The phytochemical investigation of methanol extract from M. robusta leaves yielded the known compound kaempferol (3) and two new flavonol glycosides: kaempferol-3-O-b-D-glucopyranosyl-(1 !3)-a-Lrhamnopyranosyl-( 1 ! 2)-b-D-glucopyranoside (1) and quercetin-3-O-b-D-glucopyranosyl-(1 !3)-a-Lrhamnopyranosyl-( 1 ! 2)-b-D-glucopyranoside (2). The chemical structures of 1 and 2 were elucidated by 1D/2D NMR, ESI–MS and ESI–MS2 spectral data. It is the first time flavonoids have been reported from M. robusta. Flavonols 1 and 2 showed 66% and 80% acetylcholinesterase (AChE) inhibition, compared to 93% of the standard eserine, by the Ellman’s method. These substances are one of the few active flavonols linked to a trisaccharide chain in the literature presenting this activity, and contribute to the screening for new types of natural AChE inhibitors. |
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Sousa, Grasiely Faria deAguiar, Mariana Guerra deTakahashi, Jacqueline AparecidaAlves, Tânia Maria de AlmeidaKohlhoff, MarkusVieira Filho, Sidney AugustoSilva, Grácia Divina de FátimaDuarte, Lucienir Pains2017-08-30T18:26:32Z2017-08-30T18:26:32Z2017SOUSA, G. F. et al. Flavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition. Phytochemistry Letters, v. 19, p. 34-38, 2017. Disponível em: <http://www.sciencedirect.com/science/article/pii/S1874390016302282>. Acesso em: 29 ago. 2017.1874-3900http://www.repositorio.ufop.br/handle/123456789/8611https://doi.org/10.1016/j.phytol.2016.10.024Although Maytenus robusta aqueous infusions of leaves are used in Brazilian traditional medicine for stomach disease treatment, only a few chemical studies of this species are found in literature. The phytochemical investigation of methanol extract from M. robusta leaves yielded the known compound kaempferol (3) and two new flavonol glycosides: kaempferol-3-O-b-D-glucopyranosyl-(1 !3)-a-Lrhamnopyranosyl-( 1 ! 2)-b-D-glucopyranoside (1) and quercetin-3-O-b-D-glucopyranosyl-(1 !3)-a-Lrhamnopyranosyl-( 1 ! 2)-b-D-glucopyranoside (2). The chemical structures of 1 and 2 were elucidated by 1D/2D NMR, ESI–MS and ESI–MS2 spectral data. It is the first time flavonoids have been reported from M. robusta. Flavonols 1 and 2 showed 66% and 80% acetylcholinesterase (AChE) inhibition, compared to 93% of the standard eserine, by the Ellman’s method. These substances are one of the few active flavonols linked to a trisaccharide chain in the literature presenting this activity, and contribute to the screening for new types of natural AChE inhibitors.O periódico Phytochemistry Letters concede permissão para depósito deste artigo no Repositório Institucional da UFOP. Número da licença: 4178720474114.info:eu-repo/semantics/openAccessCelastraceaeFlavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition.info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleengreponame:Repositório Institucional da UFOPinstname:Universidade Federal de Ouro Preto (UFOP)instacron:UFOPLICENSElicense.txtlicense.txttext/plain; charset=utf-8924http://www.repositorio.ufop.br/bitstream/123456789/8611/2/license.txt62604f8d955274beb56c80ce1ee5dcaeMD52ORIGINALARTIGO_FlavonolTriglycosidesLeaves.pdfARTIGO_FlavonolTriglycosidesLeaves.pdfapplication/pdf352467http://www.repositorio.ufop.br/bitstream/123456789/8611/1/ARTIGO_FlavonolTriglycosidesLeaves.pdf25e6d648b553e81ee60481acebea9259MD51123456789/86112020-01-23 06:21:08.286oai:localhost: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ório InstitucionalPUBhttp://www.repositorio.ufop.br/oai/requestrepositorio@ufop.edu.bropendoar:32332020-01-23T11:21:08Repositório Institucional da UFOP - Universidade Federal de Ouro Preto (UFOP)false |
dc.title.pt_BR.fl_str_mv |
Flavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition. |
title |
Flavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition. |
spellingShingle |
Flavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition. Sousa, Grasiely Faria de Celastraceae |
title_short |
Flavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition. |
title_full |
Flavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition. |
title_fullStr |
Flavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition. |
title_full_unstemmed |
Flavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition. |
title_sort |
Flavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition. |
author |
Sousa, Grasiely Faria de |
author_facet |
Sousa, Grasiely Faria de Aguiar, Mariana Guerra de Takahashi, Jacqueline Aparecida Alves, Tânia Maria de Almeida Kohlhoff, Markus Vieira Filho, Sidney Augusto Silva, Grácia Divina de Fátima Duarte, Lucienir Pains |
author_role |
author |
author2 |
Aguiar, Mariana Guerra de Takahashi, Jacqueline Aparecida Alves, Tânia Maria de Almeida Kohlhoff, Markus Vieira Filho, Sidney Augusto Silva, Grácia Divina de Fátima Duarte, Lucienir Pains |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Sousa, Grasiely Faria de Aguiar, Mariana Guerra de Takahashi, Jacqueline Aparecida Alves, Tânia Maria de Almeida Kohlhoff, Markus Vieira Filho, Sidney Augusto Silva, Grácia Divina de Fátima Duarte, Lucienir Pains |
dc.subject.por.fl_str_mv |
Celastraceae |
topic |
Celastraceae |
description |
Although Maytenus robusta aqueous infusions of leaves are used in Brazilian traditional medicine for stomach disease treatment, only a few chemical studies of this species are found in literature. The phytochemical investigation of methanol extract from M. robusta leaves yielded the known compound kaempferol (3) and two new flavonol glycosides: kaempferol-3-O-b-D-glucopyranosyl-(1 !3)-a-Lrhamnopyranosyl-( 1 ! 2)-b-D-glucopyranoside (1) and quercetin-3-O-b-D-glucopyranosyl-(1 !3)-a-Lrhamnopyranosyl-( 1 ! 2)-b-D-glucopyranoside (2). The chemical structures of 1 and 2 were elucidated by 1D/2D NMR, ESI–MS and ESI–MS2 spectral data. It is the first time flavonoids have been reported from M. robusta. Flavonols 1 and 2 showed 66% and 80% acetylcholinesterase (AChE) inhibition, compared to 93% of the standard eserine, by the Ellman’s method. These substances are one of the few active flavonols linked to a trisaccharide chain in the literature presenting this activity, and contribute to the screening for new types of natural AChE inhibitors. |
publishDate |
2017 |
dc.date.accessioned.fl_str_mv |
2017-08-30T18:26:32Z |
dc.date.available.fl_str_mv |
2017-08-30T18:26:32Z |
dc.date.issued.fl_str_mv |
2017 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
SOUSA, G. F. et al. Flavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition. Phytochemistry Letters, v. 19, p. 34-38, 2017. Disponível em: <http://www.sciencedirect.com/science/article/pii/S1874390016302282>. Acesso em: 29 ago. 2017. |
dc.identifier.uri.fl_str_mv |
http://www.repositorio.ufop.br/handle/123456789/8611 |
dc.identifier.issn.none.fl_str_mv |
1874-3900 |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1016/j.phytol.2016.10.024 |
identifier_str_mv |
SOUSA, G. F. et al. Flavonol triglycosides of leaves from Maytenus robusta with acetylcholinesterase inhibition. Phytochemistry Letters, v. 19, p. 34-38, 2017. Disponível em: <http://www.sciencedirect.com/science/article/pii/S1874390016302282>. Acesso em: 29 ago. 2017. 1874-3900 |
url |
http://www.repositorio.ufop.br/handle/123456789/8611 https://doi.org/10.1016/j.phytol.2016.10.024 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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info:eu-repo/semantics/openAccess |
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openAccess |
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reponame:Repositório Institucional da UFOP instname:Universidade Federal de Ouro Preto (UFOP) instacron:UFOP |
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