Chrysoeriol derivatives and other constituents from Glandularia selloi

Detalhes bibliográficos
Autor(a) principal: Vestena, Angelica
Data de Publicação: 2019
Outros Autores: Comerlato, Luana, Bridi, Henrique, Guerini, Leticia, Ccana-Ccapatinta, Gari Vidal, Vignoli-Silva, Marcia, Apel, Miriam Anders, Fernandes, Saulo, Castro-Gamboa, Ian [UNESP], Silveira Zuanazzi, Jose Angelo, von Poser, Gilsane Lino
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.phytol.2018.11.003
http://hdl.handle.net/11449/185344
Resumo: Glandularia selloi (Verbenaceae) presents phenylethanoids, iridoids and flavone glycosides as the main constituents. Two novel chrysoeriol derivatives, selloiside A (1) and selloiside B (2) were isolated from the methanolic extract of the aerial parts. Both flavones are acylated disaccharides. Two known compounds, verbascoside (3) and 6 beta-hydroxy-ipolamiide (4), were isolated from the methanolic extract of the roots. The structures were elucidated using 1D, 2D NMR and MS. Acylflavones have taxonomic significance since they occur mainly is species from the order Lamiales, specifically from the family Lamiaceae, closely related to Verbenaceae. The compounds 1 - 4 and the methanolic extract were investigated for antichemotactic activity.
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spelling Chrysoeriol derivatives and other constituents from Glandularia selloiGlandularia selloiacylated flavonesphenylethanoid glycosidesiridoidsGlandularia selloi (Verbenaceae) presents phenylethanoids, iridoids and flavone glycosides as the main constituents. Two novel chrysoeriol derivatives, selloiside A (1) and selloiside B (2) were isolated from the methanolic extract of the aerial parts. Both flavones are acylated disaccharides. Two known compounds, verbascoside (3) and 6 beta-hydroxy-ipolamiide (4), were isolated from the methanolic extract of the roots. The structures were elucidated using 1D, 2D NMR and MS. Acylflavones have taxonomic significance since they occur mainly is species from the order Lamiales, specifically from the family Lamiaceae, closely related to Verbenaceae. The compounds 1 - 4 and the methanolic extract were investigated for antichemotactic activity.FAPERGSCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)INCTBioNatUniv Fed Rio Grande do Sul, Programa Posgrad Ciencias Farmaceut, Av Ipiranga 2752, BR-90610000 Porto Alegre, RS, BrazilUniv Fed Ciencias Saude Porto Alegre, Dept Ciencias Basicas Saude, Rua Sarmento Leite 245, BR-90050170 Porto Alegre, RS, BrazilUniv Estadual Paulista, NuBBE Nucl Bioensaios Biossintese & Ecol Prod Nat, Dept Quim Organ, Rua Prof Francisco Degni 55, BR-14800060 Araraquara, BrazilUniv Estadual Paulista, NuBBE Nucl Bioensaios Biossintese & Ecol Prod Nat, Dept Quim Organ, Rua Prof Francisco Degni 55, BR-14800060 Araraquara, BrazilINCTBioNat: CNPq 465637/2014-0Elsevier B.V.Univ Fed Rio Grande do SulUniv Fed Ciencias Saude Porto AlegreUniversidade Estadual Paulista (Unesp)Vestena, AngelicaComerlato, LuanaBridi, HenriqueGuerini, LeticiaCcana-Ccapatinta, Gari VidalVignoli-Silva, MarciaApel, Miriam AndersFernandes, SauloCastro-Gamboa, Ian [UNESP]Silveira Zuanazzi, Jose Angelovon Poser, Gilsane Lino2019-10-04T12:34:43Z2019-10-04T12:34:43Z2019-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article30-34http://dx.doi.org/10.1016/j.phytol.2018.11.003Phytochemistry Letters. Amsterdam: Elsevier Science Bv, v. 29, p. 30-34, 2019.1874-3900http://hdl.handle.net/11449/18534410.1016/j.phytol.2018.11.003WOS:000456346200006Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPhytochemistry Lettersinfo:eu-repo/semantics/openAccess2021-10-23T19:23:18Zoai:repositorio.unesp.br:11449/185344Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T17:41:55.560416Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Chrysoeriol derivatives and other constituents from Glandularia selloi
title Chrysoeriol derivatives and other constituents from Glandularia selloi
spellingShingle Chrysoeriol derivatives and other constituents from Glandularia selloi
Vestena, Angelica
Glandularia selloi
acylated flavones
phenylethanoid glycosides
iridoids
title_short Chrysoeriol derivatives and other constituents from Glandularia selloi
title_full Chrysoeriol derivatives and other constituents from Glandularia selloi
title_fullStr Chrysoeriol derivatives and other constituents from Glandularia selloi
title_full_unstemmed Chrysoeriol derivatives and other constituents from Glandularia selloi
title_sort Chrysoeriol derivatives and other constituents from Glandularia selloi
author Vestena, Angelica
author_facet Vestena, Angelica
Comerlato, Luana
Bridi, Henrique
Guerini, Leticia
Ccana-Ccapatinta, Gari Vidal
Vignoli-Silva, Marcia
Apel, Miriam Anders
Fernandes, Saulo
Castro-Gamboa, Ian [UNESP]
Silveira Zuanazzi, Jose Angelo
von Poser, Gilsane Lino
author_role author
author2 Comerlato, Luana
Bridi, Henrique
Guerini, Leticia
Ccana-Ccapatinta, Gari Vidal
Vignoli-Silva, Marcia
Apel, Miriam Anders
Fernandes, Saulo
Castro-Gamboa, Ian [UNESP]
Silveira Zuanazzi, Jose Angelo
von Poser, Gilsane Lino
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Univ Fed Rio Grande do Sul
Univ Fed Ciencias Saude Porto Alegre
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Vestena, Angelica
Comerlato, Luana
Bridi, Henrique
Guerini, Leticia
Ccana-Ccapatinta, Gari Vidal
Vignoli-Silva, Marcia
Apel, Miriam Anders
Fernandes, Saulo
Castro-Gamboa, Ian [UNESP]
Silveira Zuanazzi, Jose Angelo
von Poser, Gilsane Lino
dc.subject.por.fl_str_mv Glandularia selloi
acylated flavones
phenylethanoid glycosides
iridoids
topic Glandularia selloi
acylated flavones
phenylethanoid glycosides
iridoids
description Glandularia selloi (Verbenaceae) presents phenylethanoids, iridoids and flavone glycosides as the main constituents. Two novel chrysoeriol derivatives, selloiside A (1) and selloiside B (2) were isolated from the methanolic extract of the aerial parts. Both flavones are acylated disaccharides. Two known compounds, verbascoside (3) and 6 beta-hydroxy-ipolamiide (4), were isolated from the methanolic extract of the roots. The structures were elucidated using 1D, 2D NMR and MS. Acylflavones have taxonomic significance since they occur mainly is species from the order Lamiales, specifically from the family Lamiaceae, closely related to Verbenaceae. The compounds 1 - 4 and the methanolic extract were investigated for antichemotactic activity.
publishDate 2019
dc.date.none.fl_str_mv 2019-10-04T12:34:43Z
2019-10-04T12:34:43Z
2019-02-01
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.uri.fl_str_mv http://dx.doi.org/10.1016/j.phytol.2018.11.003
Phytochemistry Letters. Amsterdam: Elsevier Science Bv, v. 29, p. 30-34, 2019.
1874-3900
http://hdl.handle.net/11449/185344
10.1016/j.phytol.2018.11.003
WOS:000456346200006
url http://dx.doi.org/10.1016/j.phytol.2018.11.003
http://hdl.handle.net/11449/185344
identifier_str_mv Phytochemistry Letters. Amsterdam: Elsevier Science Bv, v. 29, p. 30-34, 2019.
1874-3900
10.1016/j.phytol.2018.11.003
WOS:000456346200006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Phytochemistry Letters
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 30-34
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1808128846538473472

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