A new antifungal phenolic glycoside derivative and iridoids and lignans from Alibertia sessilis (Vell.) K. Schum. (Rubiaceae)
| Autor(a) principal: | |
|---|---|
| Data de Publicação: | 2007 |
| Outros Autores: | , , |
| Tipo de documento: | Artigo |
| Idioma: | eng |
| Título da fonte: | Repositório Institucional da UNESP |
| Texto Completo: | http://dx.doi.org/10.1590/S0103-50532007000700017 http://hdl.handle.net/11449/70216 |
Resumo: | A new antifungal phenolic glycoside, 3,4,5-trimethoxyphenyl-1-O-β-D- (5-O-syringoyl)-apiofuranosyl-(1→6)-β-D-glucopyranoside (1), together with four known iridoids, geniposidic acid (2), geniposide (3), 6α-hydroxygeniposide (4) and 6β-hydroxygeniposide (5); two lignans, (+)-lyoniresinol-3α-O-β-D-glucopyranoside (6), (-)-lyoniresinol- 3α-O-β-D-glucopyranoside (7); and two phenolic acids, chlorogenic (8) and salicylic acids (9) and D-manitol (10), were isolated from the ethanolic extract of the stems of Alibertia sessilis. Structures of 1 and of the known compounds were determined by spectroscopic analysis. All compounds isolated were evaluated for their antifungal activities against two phytopathogenic fungi strains Cladosporium cladosporioides and C. sphaerospermum by direct bioautography. ©2007 Sociedade Brasileira de Química. |
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A new antifungal phenolic glycoside derivative and iridoids and lignans from Alibertia sessilis (Vell.) K. Schum. (Rubiaceae)Alibertia sessilisAntifungalIridoidsPhenolicsRubiaceaeA new antifungal phenolic glycoside, 3,4,5-trimethoxyphenyl-1-O-β-D- (5-O-syringoyl)-apiofuranosyl-(1→6)-β-D-glucopyranoside (1), together with four known iridoids, geniposidic acid (2), geniposide (3), 6α-hydroxygeniposide (4) and 6β-hydroxygeniposide (5); two lignans, (+)-lyoniresinol-3α-O-β-D-glucopyranoside (6), (-)-lyoniresinol- 3α-O-β-D-glucopyranoside (7); and two phenolic acids, chlorogenic (8) and salicylic acids (9) and D-manitol (10), were isolated from the ethanolic extract of the stems of Alibertia sessilis. Structures of 1 and of the known compounds were determined by spectroscopic analysis. All compounds isolated were evaluated for their antifungal activities against two phytopathogenic fungi strains Cladosporium cladosporioides and C. sphaerospermum by direct bioautography. ©2007 Sociedade Brasileira de Química.Departamento de Química Orgânica Instituto de Química Universidade Estadual Paulista, CP 355, 14801-970 Araraquara-SPSeção de Fisiologia e Bioquímica de Plantas Instituto de Botânica, CP 4005, 01061-970 São Paulo-SPDepartamento de Química Orgânica Instituto de Química Universidade Estadual Paulista, CP 355, 14801-970 Araraquara-SPUniversidade Estadual Paulista (Unesp)Instituto de BotânicaSilva, Viviane C. da [UNESP]Bolzani, Vanderlan da Silva [UNESP]Young, Maria C. M.Lopes, Márcia Nasser [UNESP]2014-05-27T11:22:45Z2014-05-27T11:22:45Z2007-12-17info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1405-1409application/pdfhttp://dx.doi.org/10.1590/S0103-50532007000700017Journal of the Brazilian Chemical Society, v. 18, n. 7, p. 1405-1409, 2007.0103-50531678-4790http://hdl.handle.net/11449/7021610.1590/S0103-50532007000700017S0103-50532007000700017WOS:0002521890000172-s2.0-369490379862-s2.0-36949037986.pdf44840836852516733310170899693944Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of the Brazilian Chemical Society1.4440,3570,357info:eu-repo/semantics/openAccess2023-11-10T06:16:12Zoai:repositorio.unesp.br:11449/70216Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T17:21:05.404522Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
| dc.title.none.fl_str_mv |
A new antifungal phenolic glycoside derivative and iridoids and lignans from Alibertia sessilis (Vell.) K. Schum. (Rubiaceae) |
| title |
A new antifungal phenolic glycoside derivative and iridoids and lignans from Alibertia sessilis (Vell.) K. Schum. (Rubiaceae) |
| spellingShingle |
A new antifungal phenolic glycoside derivative and iridoids and lignans from Alibertia sessilis (Vell.) K. Schum. (Rubiaceae) Silva, Viviane C. da [UNESP] Alibertia sessilis Antifungal Iridoids Phenolics Rubiaceae |
| title_short |
A new antifungal phenolic glycoside derivative and iridoids and lignans from Alibertia sessilis (Vell.) K. Schum. (Rubiaceae) |
| title_full |
A new antifungal phenolic glycoside derivative and iridoids and lignans from Alibertia sessilis (Vell.) K. Schum. (Rubiaceae) |
| title_fullStr |
A new antifungal phenolic glycoside derivative and iridoids and lignans from Alibertia sessilis (Vell.) K. Schum. (Rubiaceae) |
| title_full_unstemmed |
A new antifungal phenolic glycoside derivative and iridoids and lignans from Alibertia sessilis (Vell.) K. Schum. (Rubiaceae) |
| title_sort |
A new antifungal phenolic glycoside derivative and iridoids and lignans from Alibertia sessilis (Vell.) K. Schum. (Rubiaceae) |
| author |
Silva, Viviane C. da [UNESP] |
| author_facet |
Silva, Viviane C. da [UNESP] Bolzani, Vanderlan da Silva [UNESP] Young, Maria C. M. Lopes, Márcia Nasser [UNESP] |
| author_role |
author |
| author2 |
Bolzani, Vanderlan da Silva [UNESP] Young, Maria C. M. Lopes, Márcia Nasser [UNESP] |
| author2_role |
author author author |
| dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Instituto de Botânica |
| dc.contributor.author.fl_str_mv |
Silva, Viviane C. da [UNESP] Bolzani, Vanderlan da Silva [UNESP] Young, Maria C. M. Lopes, Márcia Nasser [UNESP] |
| dc.subject.por.fl_str_mv |
Alibertia sessilis Antifungal Iridoids Phenolics Rubiaceae |
| topic |
Alibertia sessilis Antifungal Iridoids Phenolics Rubiaceae |
| description |
A new antifungal phenolic glycoside, 3,4,5-trimethoxyphenyl-1-O-β-D- (5-O-syringoyl)-apiofuranosyl-(1→6)-β-D-glucopyranoside (1), together with four known iridoids, geniposidic acid (2), geniposide (3), 6α-hydroxygeniposide (4) and 6β-hydroxygeniposide (5); two lignans, (+)-lyoniresinol-3α-O-β-D-glucopyranoside (6), (-)-lyoniresinol- 3α-O-β-D-glucopyranoside (7); and two phenolic acids, chlorogenic (8) and salicylic acids (9) and D-manitol (10), were isolated from the ethanolic extract of the stems of Alibertia sessilis. Structures of 1 and of the known compounds were determined by spectroscopic analysis. All compounds isolated were evaluated for their antifungal activities against two phytopathogenic fungi strains Cladosporium cladosporioides and C. sphaerospermum by direct bioautography. ©2007 Sociedade Brasileira de Química. |
| publishDate |
2007 |
| dc.date.none.fl_str_mv |
2007-12-17 2014-05-27T11:22:45Z 2014-05-27T11:22:45Z |
| 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/10.1590/S0103-50532007000700017 Journal of the Brazilian Chemical Society, v. 18, n. 7, p. 1405-1409, 2007. 0103-5053 1678-4790 http://hdl.handle.net/11449/70216 10.1590/S0103-50532007000700017 S0103-50532007000700017 WOS:000252189000017 2-s2.0-36949037986 2-s2.0-36949037986.pdf 4484083685251673 3310170899693944 |
| url |
http://dx.doi.org/10.1590/S0103-50532007000700017 http://hdl.handle.net/11449/70216 |
| identifier_str_mv |
Journal of the Brazilian Chemical Society, v. 18, n. 7, p. 1405-1409, 2007. 0103-5053 1678-4790 10.1590/S0103-50532007000700017 S0103-50532007000700017 WOS:000252189000017 2-s2.0-36949037986 2-s2.0-36949037986.pdf 4484083685251673 3310170899693944 |
| dc.language.iso.fl_str_mv |
eng |
| language |
eng |
| dc.relation.none.fl_str_mv |
Journal of the Brazilian Chemical Society 1.444 0,357 0,357 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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1405-1409 application/pdf |
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Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
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Universidade Estadual Paulista (UNESP) |
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UNESP |
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UNESP |
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Repositório Institucional da UNESP |
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Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
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