Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial parts
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Revista Brasileira de Farmacognosia (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2018000300320 |
Resumo: | ABSTRACT Cyperus rotundus L. (Suada, Sueda, family: Cyperaceae) is vastly spread in several world's subtropical and tropical regions. It had variable traditional uses and bioactivities. A new flavonol derivative: cyperaflavoside (myricetin 3,3',5'-trimethyl ether 7-O-β-D-glucopyranoside) and five flavonoids: vitexin, orientin, cinaroside, quercetin 3-O-β-D-glucopyranoside, and myrcetin 3-O-β-D-glucopyranoside were separated from the methanolic extract of C. rotundus aerial parts. Their structures were verified based on UV, IR, NMR (1D and 2D), HRESIMS, and comparison with literature. All metabolites were assessed for their 5-lipoxygenase inhibitory potential. All compounds possessed 5-lipoxygenase inhibitory potentials with IC50s 5.1, 4.5, 5.9, 4.0, 3.7, and 2.3 µM, respectively, in comparison to indomethacin (IC50 0.98 µM). These results supported the traditional uses of C. rotundus in treating inflammation and its related symptoms. |
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Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial partsCyperaceaeFlavonolsMyricetin derivative5-Lipoxygenase inhibitorInflammationStructural activity relationshipABSTRACT Cyperus rotundus L. (Suada, Sueda, family: Cyperaceae) is vastly spread in several world's subtropical and tropical regions. It had variable traditional uses and bioactivities. A new flavonol derivative: cyperaflavoside (myricetin 3,3',5'-trimethyl ether 7-O-β-D-glucopyranoside) and five flavonoids: vitexin, orientin, cinaroside, quercetin 3-O-β-D-glucopyranoside, and myrcetin 3-O-β-D-glucopyranoside were separated from the methanolic extract of C. rotundus aerial parts. Their structures were verified based on UV, IR, NMR (1D and 2D), HRESIMS, and comparison with literature. All metabolites were assessed for their 5-lipoxygenase inhibitory potential. All compounds possessed 5-lipoxygenase inhibitory potentials with IC50s 5.1, 4.5, 5.9, 4.0, 3.7, and 2.3 µM, respectively, in comparison to indomethacin (IC50 0.98 µM). These results supported the traditional uses of C. rotundus in treating inflammation and its related symptoms.Sociedade Brasileira de Farmacognosia2018-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2018000300320Revista Brasileira de Farmacognosia v.28 n.3 2018reponame:Revista Brasileira de Farmacognosia (Online)instname:Sociedade Brasileira de Farmacognosia (SBFgnosia)instacron:SBFGNOSIA10.1016/j.bjp.2018.04.002info:eu-repo/semantics/openAccessIbrahim,Sabrin R.M.Mohamed,Gamal A.Alshali,Khalid Z.Haidari,Rwaida A. AlEl-Kholy,Amal A.Zayed,Mohamed F.eng2018-07-03T00:00:00Zoai:scielo:S0102-695X2018000300320Revistahttp://www.sbfgnosia.org.br/revista/https://old.scielo.br/oai/scielo-oai.phprbgnosia@ltf.ufpb.br1981-528X0102-695Xopendoar:2018-07-03T00:00Revista Brasileira de Farmacognosia (Online) - Sociedade Brasileira de Farmacognosia (SBFgnosia)false |
dc.title.none.fl_str_mv |
Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial parts |
title |
Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial parts |
spellingShingle |
Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial parts Ibrahim,Sabrin R.M. Cyperaceae Flavonols Myricetin derivative 5-Lipoxygenase inhibitor Inflammation Structural activity relationship |
title_short |
Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial parts |
title_full |
Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial parts |
title_fullStr |
Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial parts |
title_full_unstemmed |
Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial parts |
title_sort |
Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial parts |
author |
Ibrahim,Sabrin R.M. |
author_facet |
Ibrahim,Sabrin R.M. Mohamed,Gamal A. Alshali,Khalid Z. Haidari,Rwaida A. Al El-Kholy,Amal A. Zayed,Mohamed F. |
author_role |
author |
author2 |
Mohamed,Gamal A. Alshali,Khalid Z. Haidari,Rwaida A. Al El-Kholy,Amal A. Zayed,Mohamed F. |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Ibrahim,Sabrin R.M. Mohamed,Gamal A. Alshali,Khalid Z. Haidari,Rwaida A. Al El-Kholy,Amal A. Zayed,Mohamed F. |
dc.subject.por.fl_str_mv |
Cyperaceae Flavonols Myricetin derivative 5-Lipoxygenase inhibitor Inflammation Structural activity relationship |
topic |
Cyperaceae Flavonols Myricetin derivative 5-Lipoxygenase inhibitor Inflammation Structural activity relationship |
description |
ABSTRACT Cyperus rotundus L. (Suada, Sueda, family: Cyperaceae) is vastly spread in several world's subtropical and tropical regions. It had variable traditional uses and bioactivities. A new flavonol derivative: cyperaflavoside (myricetin 3,3',5'-trimethyl ether 7-O-β-D-glucopyranoside) and five flavonoids: vitexin, orientin, cinaroside, quercetin 3-O-β-D-glucopyranoside, and myrcetin 3-O-β-D-glucopyranoside were separated from the methanolic extract of C. rotundus aerial parts. Their structures were verified based on UV, IR, NMR (1D and 2D), HRESIMS, and comparison with literature. All metabolites were assessed for their 5-lipoxygenase inhibitory potential. All compounds possessed 5-lipoxygenase inhibitory potentials with IC50s 5.1, 4.5, 5.9, 4.0, 3.7, and 2.3 µM, respectively, in comparison to indomethacin (IC50 0.98 µM). These results supported the traditional uses of C. rotundus in treating inflammation and its related symptoms. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-06-01 |
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=S0102-695X2018000300320 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2018000300320 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1016/j.bjp.2018.04.002 |
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 Farmacognosia |
publisher.none.fl_str_mv |
Sociedade Brasileira de Farmacognosia |
dc.source.none.fl_str_mv |
Revista Brasileira de Farmacognosia v.28 n.3 2018 reponame:Revista Brasileira de Farmacognosia (Online) instname:Sociedade Brasileira de Farmacognosia (SBFgnosia) instacron:SBFGNOSIA |
instname_str |
Sociedade Brasileira de Farmacognosia (SBFgnosia) |
instacron_str |
SBFGNOSIA |
institution |
SBFGNOSIA |
reponame_str |
Revista Brasileira de Farmacognosia (Online) |
collection |
Revista Brasileira de Farmacognosia (Online) |
repository.name.fl_str_mv |
Revista Brasileira de Farmacognosia (Online) - Sociedade Brasileira de Farmacognosia (SBFgnosia) |
repository.mail.fl_str_mv |
rbgnosia@ltf.ufpb.br |
_version_ |
1752122470682329088 |