A New Isoflavone and Other Constituents from Roots of Clitoria guianensis

Detalhes bibliográficos
Autor(a) principal: Cunha, Camila L. [UNESP]
Data de Publicação: 2020
Outros Autores: Siebeneichler, Susana C., Nascimento, Isabele R. [UNESP], Holzbach, Juliana C.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.21577/0103-5053.20200061
http://hdl.handle.net/11449/195510
Resumo: A new isoflavone named pratensein-7-O-beta-D-rutinoside [(-)-7-O-alpha-L-rhamnopyranosyl(1 -> 6)-beta-D-glucopyranosy1-5,3'-dihydroxy-4'-methoxyisoflavone] and the known compounds biochanin A-7-O-beta-D-rutinoside. 6-deoxyclitoriacetal A-O-beta-D-glucopyranoside. 6-deoxyclitoriacetal. (2S)-naringenin-6-C-beta-D-glucopyranoside. (2R)-naringenin-6-C-beta-D-glucopyranoside, tachioside, and koaburaside were isolated from the roots of Clitoria guianensis (Aubl.) Benth var. guianensis (Fabaceae), a subshrub found in the Brazilian Cerrado biome. The structures of the compounds were identified by physical and spectroscopic data measurements (specific rotation ([alpha](D)), circular dichroism (CD), ultraviolet (UV), infrared (IR), 1D and 2D nuclear magnetic resonance (NMR), and mass spectrometry (MS)). The EtOAc fraction of the roots exhibited high toxicity against Anemia salina with median lethal dose (LD50) value of 8.53 mg L-1.
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spelling A New Isoflavone and Other Constituents from Roots of Clitoria guianensisClitoria guianensisFabaceaeisoflavoneflavanoneA new isoflavone named pratensein-7-O-beta-D-rutinoside [(-)-7-O-alpha-L-rhamnopyranosyl(1 -> 6)-beta-D-glucopyranosy1-5,3'-dihydroxy-4'-methoxyisoflavone] and the known compounds biochanin A-7-O-beta-D-rutinoside. 6-deoxyclitoriacetal A-O-beta-D-glucopyranoside. 6-deoxyclitoriacetal. (2S)-naringenin-6-C-beta-D-glucopyranoside. (2R)-naringenin-6-C-beta-D-glucopyranoside, tachioside, and koaburaside were isolated from the roots of Clitoria guianensis (Aubl.) Benth var. guianensis (Fabaceae), a subshrub found in the Brazilian Cerrado biome. The structures of the compounds were identified by physical and spectroscopic data measurements (specific rotation ([alpha](D)), circular dichroism (CD), ultraviolet (UV), infrared (IR), 1D and 2D nuclear magnetic resonance (NMR), and mass spectrometry (MS)). The EtOAc fraction of the roots exhibited high toxicity against Anemia salina with median lethal dose (LD50) value of 8.53 mg L-1.FINEPUniv Estadual Paulista Unesp, Inst Quim, BR-14800060 Araraquara, SP, BrazilUniv Fed Tocantins UFT, CP 66, BR-77402970 Gurupi, TO, BrazilUniv Estadual Paulista Unesp, Inst Quim, BR-14800060 Araraquara, SP, BrazilSoc Brasileira QuimicaUniversidade Estadual Paulista (Unesp)Univ Fed Tocantins UFTCunha, Camila L. [UNESP]Siebeneichler, Susana C.Nascimento, Isabele R. [UNESP]Holzbach, Juliana C.2020-12-10T17:37:01Z2020-12-10T17:37:01Z2020-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1753-1757application/pdfhttp://dx.doi.org/10.21577/0103-5053.20200061Journal Of The Brazilian Chemical Society. Sao Paulo: Soc Brasileira Quimica, v. 31, n. 8, p. 1753-1757, 2020.0103-5053http://hdl.handle.net/11449/19551010.21577/0103-5053.20200061S0103-50532020000801753WOS:000547872700022S0103-50532020000801753.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of The Brazilian Chemical Societyinfo:eu-repo/semantics/openAccess2023-11-24T06:17:23Zoai:repositorio.unesp.br:11449/195510Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T18:38:31.080357Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv A New Isoflavone and Other Constituents from Roots of Clitoria guianensis
title A New Isoflavone and Other Constituents from Roots of Clitoria guianensis
spellingShingle A New Isoflavone and Other Constituents from Roots of Clitoria guianensis
Cunha, Camila L. [UNESP]
Clitoria guianensis
Fabaceae
isoflavone
flavanone
title_short A New Isoflavone and Other Constituents from Roots of Clitoria guianensis
title_full A New Isoflavone and Other Constituents from Roots of Clitoria guianensis
title_fullStr A New Isoflavone and Other Constituents from Roots of Clitoria guianensis
title_full_unstemmed A New Isoflavone and Other Constituents from Roots of Clitoria guianensis
title_sort A New Isoflavone and Other Constituents from Roots of Clitoria guianensis
author Cunha, Camila L. [UNESP]
author_facet Cunha, Camila L. [UNESP]
Siebeneichler, Susana C.
Nascimento, Isabele R. [UNESP]
Holzbach, Juliana C.
author_role author
author2 Siebeneichler, Susana C.
Nascimento, Isabele R. [UNESP]
Holzbach, Juliana C.
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Univ Fed Tocantins UFT
dc.contributor.author.fl_str_mv Cunha, Camila L. [UNESP]
Siebeneichler, Susana C.
Nascimento, Isabele R. [UNESP]
Holzbach, Juliana C.
dc.subject.por.fl_str_mv Clitoria guianensis
Fabaceae
isoflavone
flavanone
topic Clitoria guianensis
Fabaceae
isoflavone
flavanone
description A new isoflavone named pratensein-7-O-beta-D-rutinoside [(-)-7-O-alpha-L-rhamnopyranosyl(1 -> 6)-beta-D-glucopyranosy1-5,3'-dihydroxy-4'-methoxyisoflavone] and the known compounds biochanin A-7-O-beta-D-rutinoside. 6-deoxyclitoriacetal A-O-beta-D-glucopyranoside. 6-deoxyclitoriacetal. (2S)-naringenin-6-C-beta-D-glucopyranoside. (2R)-naringenin-6-C-beta-D-glucopyranoside, tachioside, and koaburaside were isolated from the roots of Clitoria guianensis (Aubl.) Benth var. guianensis (Fabaceae), a subshrub found in the Brazilian Cerrado biome. The structures of the compounds were identified by physical and spectroscopic data measurements (specific rotation ([alpha](D)), circular dichroism (CD), ultraviolet (UV), infrared (IR), 1D and 2D nuclear magnetic resonance (NMR), and mass spectrometry (MS)). The EtOAc fraction of the roots exhibited high toxicity against Anemia salina with median lethal dose (LD50) value of 8.53 mg L-1.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-10T17:37:01Z
2020-12-10T17:37:01Z
2020-08-01
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/10.21577/0103-5053.20200061
Journal Of The Brazilian Chemical Society. Sao Paulo: Soc Brasileira Quimica, v. 31, n. 8, p. 1753-1757, 2020.
0103-5053
http://hdl.handle.net/11449/195510
10.21577/0103-5053.20200061
S0103-50532020000801753
WOS:000547872700022
S0103-50532020000801753.pdf
url http://dx.doi.org/10.21577/0103-5053.20200061
http://hdl.handle.net/11449/195510
identifier_str_mv Journal Of The Brazilian Chemical Society. Sao Paulo: Soc Brasileira Quimica, v. 31, n. 8, p. 1753-1757, 2020.
0103-5053
10.21577/0103-5053.20200061
S0103-50532020000801753
WOS:000547872700022
S0103-50532020000801753.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal Of The Brazilian Chemical Society
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1753-1757
application/pdf
dc.publisher.none.fl_str_mv Soc Brasileira Quimica
publisher.none.fl_str_mv Soc Brasileira Quimica
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)
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