The Antigerminative Activity of Twenty-Seven Monoterpenes
Autor(a) principal: | |
---|---|
Data de Publicação: | 2010 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.3390/molecules15096630 http://hdl.handle.net/11449/17364 |
Resumo: | Monoterpenes, the main constituents of essential oils, are known for their many biological activities. The present work studied the potential biological activity of twenty-seven monoterpenes, including monoterpene hydrocarbons and oxygenated ones, against seed germination and subsequent primary radicle growth of Raphanus sativus L. (radish) and Lepidium sativum L. (garden cress), under laboratory conditions. The compounds, belonging to different chemical classes, showed different potency in affecting both parameters evaluated. The assayed compounds demonstrated a good inhibitory activity in a dose-dependent way. In general, radish seed is more sensitive than garden cress and its germination appeares more inhibited by alcohols; at the highest concentration tested, the more active substances were geraniol, borneol, (+/-)-beta-citronellol and alpha-terpineol. Geraniol and carvone inhibited, in a significant way, the germination of garden cress, at the highest concentration tested. Radicle elongation of two test species was inhibited mainly by alcohols and ketones. Carvone inhibited the radicle elongation of both seeds, at almost all concentrations assayed, while 1,8-cineole inhibited their radicle elongation at the lowest concentrations (10(-5) M, 10(-6) M). |
id |
UNSP_d2c0c4fffd7817f32e92335418f6f819 |
---|---|
oai_identifier_str |
oai:repositorio.unesp.br:11449/17364 |
network_acronym_str |
UNSP |
network_name_str |
Repositório Institucional da UNESP |
repository_id_str |
2946 |
spelling |
The Antigerminative Activity of Twenty-Seven Monoterpenesmonoterpenesgerminationradicle elongationphytotoxicityMonoterpenes, the main constituents of essential oils, are known for their many biological activities. The present work studied the potential biological activity of twenty-seven monoterpenes, including monoterpene hydrocarbons and oxygenated ones, against seed germination and subsequent primary radicle growth of Raphanus sativus L. (radish) and Lepidium sativum L. (garden cress), under laboratory conditions. The compounds, belonging to different chemical classes, showed different potency in affecting both parameters evaluated. The assayed compounds demonstrated a good inhibitory activity in a dose-dependent way. In general, radish seed is more sensitive than garden cress and its germination appeares more inhibited by alcohols; at the highest concentration tested, the more active substances were geraniol, borneol, (+/-)-beta-citronellol and alpha-terpineol. Geraniol and carvone inhibited, in a significant way, the germination of garden cress, at the highest concentration tested. Radicle elongation of two test species was inhibited mainly by alcohols and ketones. Carvone inhibited the radicle elongation of both seeds, at almost all concentrations assayed, while 1,8-cineole inhibited their radicle elongation at the lowest concentrations (10(-5) M, 10(-6) M).Univ Salerno, Dipartimento Sci Farmaceut, I-84084 Salerno, ItalyUNESP, Dept Bot, Inst Biociencias Botucatu, BR-18618000 Botucatu, SP, BrazilUNESP, Dept Bot, Inst Biociencias Botucatu, BR-18618000 Botucatu, SP, BrazilMdpi AgUniv SalernoUniversidade Estadual Paulista (Unesp)De Martino, LauraMancini, EmiliaRolim de Almeida, Luiz Fernando [UNESP]De Feo, Vincenzo2014-05-20T13:48:46Z2014-05-20T13:48:46Z2010-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article6630-6637application/pdfhttp://dx.doi.org/10.3390/molecules15096630Molecules. Basel: Mdpi Ag, v. 15, n. 9, p. 6630-6637, 2010.1420-3049http://hdl.handle.net/11449/1736410.3390/molecules15096630WOS:000282221100055WOS000282221100055.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMolecules3.0980,855info:eu-repo/semantics/openAccess2023-10-31T06:10:31Zoai:repositorio.unesp.br:11449/17364Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T16:31:58.879635Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
The Antigerminative Activity of Twenty-Seven Monoterpenes |
title |
The Antigerminative Activity of Twenty-Seven Monoterpenes |
spellingShingle |
The Antigerminative Activity of Twenty-Seven Monoterpenes De Martino, Laura monoterpenes germination radicle elongation phytotoxicity |
title_short |
The Antigerminative Activity of Twenty-Seven Monoterpenes |
title_full |
The Antigerminative Activity of Twenty-Seven Monoterpenes |
title_fullStr |
The Antigerminative Activity of Twenty-Seven Monoterpenes |
title_full_unstemmed |
The Antigerminative Activity of Twenty-Seven Monoterpenes |
title_sort |
The Antigerminative Activity of Twenty-Seven Monoterpenes |
author |
De Martino, Laura |
author_facet |
De Martino, Laura Mancini, Emilia Rolim de Almeida, Luiz Fernando [UNESP] De Feo, Vincenzo |
author_role |
author |
author2 |
Mancini, Emilia Rolim de Almeida, Luiz Fernando [UNESP] De Feo, Vincenzo |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Univ Salerno Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
De Martino, Laura Mancini, Emilia Rolim de Almeida, Luiz Fernando [UNESP] De Feo, Vincenzo |
dc.subject.por.fl_str_mv |
monoterpenes germination radicle elongation phytotoxicity |
topic |
monoterpenes germination radicle elongation phytotoxicity |
description |
Monoterpenes, the main constituents of essential oils, are known for their many biological activities. The present work studied the potential biological activity of twenty-seven monoterpenes, including monoterpene hydrocarbons and oxygenated ones, against seed germination and subsequent primary radicle growth of Raphanus sativus L. (radish) and Lepidium sativum L. (garden cress), under laboratory conditions. The compounds, belonging to different chemical classes, showed different potency in affecting both parameters evaluated. The assayed compounds demonstrated a good inhibitory activity in a dose-dependent way. In general, radish seed is more sensitive than garden cress and its germination appeares more inhibited by alcohols; at the highest concentration tested, the more active substances were geraniol, borneol, (+/-)-beta-citronellol and alpha-terpineol. Geraniol and carvone inhibited, in a significant way, the germination of garden cress, at the highest concentration tested. Radicle elongation of two test species was inhibited mainly by alcohols and ketones. Carvone inhibited the radicle elongation of both seeds, at almost all concentrations assayed, while 1,8-cineole inhibited their radicle elongation at the lowest concentrations (10(-5) M, 10(-6) M). |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-09-01 2014-05-20T13:48:46Z 2014-05-20T13:48:46Z |
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/10.3390/molecules15096630 Molecules. Basel: Mdpi Ag, v. 15, n. 9, p. 6630-6637, 2010. 1420-3049 http://hdl.handle.net/11449/17364 10.3390/molecules15096630 WOS:000282221100055 WOS000282221100055.pdf |
url |
http://dx.doi.org/10.3390/molecules15096630 http://hdl.handle.net/11449/17364 |
identifier_str_mv |
Molecules. Basel: Mdpi Ag, v. 15, n. 9, p. 6630-6637, 2010. 1420-3049 10.3390/molecules15096630 WOS:000282221100055 WOS000282221100055.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Molecules 3.098 0,855 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
6630-6637 application/pdf |
dc.publisher.none.fl_str_mv |
Mdpi Ag |
publisher.none.fl_str_mv |
Mdpi Ag |
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_ |
1808128668235464704 |