Volatile Constituents of Floral Scents from Encyclia cordigera (Kunth) Dressler and E. randii (Barb. Rodr.) Porto & Brade (Orchidaceae)
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Journal of the Brazilian Chemical Society (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532022000100096 |
Resumo: | Encyclia cordigera is native from Central America tropical region, and Encyclia randii occurs at Brazilian Amazon environment domains. Floral concentrates from both Encyclia species were extracted, analyzed by gas chromatography-mass spectrometry, and identified compounds belong to terpenoids, phenylpropanoids, and fatty acid derivatives classes. Primary constituents of the E. cordigera floral scent were β-ionol (45.4%), terpinen-4-ol (12.4%), benzyl benzoate (5.6%), and indole (5.0%). (2E,6Z)-Farnesol (24.9%), heptanal (11.8%), (E)-nerolidol (9.4%), nonanal (6.4%), p-vinyl-guaiacol (6.0%), and phenylethyl benzoate (5.3%) have predominated in the floral scent of E. randii. From the olfactory standpoint, E. cordigera scent was previously characterized as a blend of ionone-floral and aromatic-floral notes. Very likely, E. randii scent presents the woody fragrance due to sesquiterpenes (2E,6Z)-farnesol and (E)-nerolidol and the fruity note from the aldehydes heptanal and nonanal. Floral perfume plays a fundamental role in attracting pollinating insects, whose symbiosis contributes to the appearance of chemical variations in orchid species. |
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Volatile Constituents of Floral Scents from Encyclia cordigera (Kunth) Dressler and E. randii (Barb. Rodr.) Porto & Brade (Orchidaceae)Orchidaceaefloral scentsβ-ionol(2E,6Z)-farnesolvolatile concentratesEncyclia cordigera is native from Central America tropical region, and Encyclia randii occurs at Brazilian Amazon environment domains. Floral concentrates from both Encyclia species were extracted, analyzed by gas chromatography-mass spectrometry, and identified compounds belong to terpenoids, phenylpropanoids, and fatty acid derivatives classes. Primary constituents of the E. cordigera floral scent were β-ionol (45.4%), terpinen-4-ol (12.4%), benzyl benzoate (5.6%), and indole (5.0%). (2E,6Z)-Farnesol (24.9%), heptanal (11.8%), (E)-nerolidol (9.4%), nonanal (6.4%), p-vinyl-guaiacol (6.0%), and phenylethyl benzoate (5.3%) have predominated in the floral scent of E. randii. From the olfactory standpoint, E. cordigera scent was previously characterized as a blend of ionone-floral and aromatic-floral notes. Very likely, E. randii scent presents the woody fragrance due to sesquiterpenes (2E,6Z)-farnesol and (E)-nerolidol and the fruity note from the aldehydes heptanal and nonanal. Floral perfume plays a fundamental role in attracting pollinating insects, whose symbiosis contributes to the appearance of chemical variations in orchid species.Sociedade Brasileira de Química2022-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532022000100096Journal of the Brazilian Chemical Society v.33 n.1 2022reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20210127info:eu-repo/semantics/openAccessVasconcelos,Franciléia M. deAndrade,Eloisa Helena A.Teixeira,Luiz Otávio A.Maia,José Guilherme S.eng2022-01-06T00:00:00Zoai:scielo:S0103-50532022000100096Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2022-01-06T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Volatile Constituents of Floral Scents from Encyclia cordigera (Kunth) Dressler and E. randii (Barb. Rodr.) Porto & Brade (Orchidaceae) |
title |
Volatile Constituents of Floral Scents from Encyclia cordigera (Kunth) Dressler and E. randii (Barb. Rodr.) Porto & Brade (Orchidaceae) |
spellingShingle |
Volatile Constituents of Floral Scents from Encyclia cordigera (Kunth) Dressler and E. randii (Barb. Rodr.) Porto & Brade (Orchidaceae) Vasconcelos,Franciléia M. de Orchidaceae floral scents β-ionol (2E,6Z)-farnesol volatile concentrates |
title_short |
Volatile Constituents of Floral Scents from Encyclia cordigera (Kunth) Dressler and E. randii (Barb. Rodr.) Porto & Brade (Orchidaceae) |
title_full |
Volatile Constituents of Floral Scents from Encyclia cordigera (Kunth) Dressler and E. randii (Barb. Rodr.) Porto & Brade (Orchidaceae) |
title_fullStr |
Volatile Constituents of Floral Scents from Encyclia cordigera (Kunth) Dressler and E. randii (Barb. Rodr.) Porto & Brade (Orchidaceae) |
title_full_unstemmed |
Volatile Constituents of Floral Scents from Encyclia cordigera (Kunth) Dressler and E. randii (Barb. Rodr.) Porto & Brade (Orchidaceae) |
title_sort |
Volatile Constituents of Floral Scents from Encyclia cordigera (Kunth) Dressler and E. randii (Barb. Rodr.) Porto & Brade (Orchidaceae) |
author |
Vasconcelos,Franciléia M. de |
author_facet |
Vasconcelos,Franciléia M. de Andrade,Eloisa Helena A. Teixeira,Luiz Otávio A. Maia,José Guilherme S. |
author_role |
author |
author2 |
Andrade,Eloisa Helena A. Teixeira,Luiz Otávio A. Maia,José Guilherme S. |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Vasconcelos,Franciléia M. de Andrade,Eloisa Helena A. Teixeira,Luiz Otávio A. Maia,José Guilherme S. |
dc.subject.por.fl_str_mv |
Orchidaceae floral scents β-ionol (2E,6Z)-farnesol volatile concentrates |
topic |
Orchidaceae floral scents β-ionol (2E,6Z)-farnesol volatile concentrates |
description |
Encyclia cordigera is native from Central America tropical region, and Encyclia randii occurs at Brazilian Amazon environment domains. Floral concentrates from both Encyclia species were extracted, analyzed by gas chromatography-mass spectrometry, and identified compounds belong to terpenoids, phenylpropanoids, and fatty acid derivatives classes. Primary constituents of the E. cordigera floral scent were β-ionol (45.4%), terpinen-4-ol (12.4%), benzyl benzoate (5.6%), and indole (5.0%). (2E,6Z)-Farnesol (24.9%), heptanal (11.8%), (E)-nerolidol (9.4%), nonanal (6.4%), p-vinyl-guaiacol (6.0%), and phenylethyl benzoate (5.3%) have predominated in the floral scent of E. randii. From the olfactory standpoint, E. cordigera scent was previously characterized as a blend of ionone-floral and aromatic-floral notes. Very likely, E. randii scent presents the woody fragrance due to sesquiterpenes (2E,6Z)-farnesol and (E)-nerolidol and the fruity note from the aldehydes heptanal and nonanal. Floral perfume plays a fundamental role in attracting pollinating insects, whose symbiosis contributes to the appearance of chemical variations in orchid species. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532022000100096 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532022000100096 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.21577/0103-5053.20210127 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
dc.source.none.fl_str_mv |
Journal of the Brazilian Chemical Society v.33 n.1 2022 reponame:Journal of the Brazilian Chemical Society (Online) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
instname_str |
Sociedade Brasileira de Química (SBQ) |
instacron_str |
SBQ |
institution |
SBQ |
reponame_str |
Journal of the Brazilian Chemical Society (Online) |
collection |
Journal of the Brazilian Chemical Society (Online) |
repository.name.fl_str_mv |
Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ) |
repository.mail.fl_str_mv |
||office@jbcs.sbq.org.br |
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1750318184777383936 |