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Lipoperoxidation and cyclooxygenases 1 and 2 inhibitory compounds from Iryanthera juruensis

dc.contributor.authorSilva, Dulce Helena Siqueira [UNESP]
dc.contributor.authorZhang, Yanjun
dc.contributor.authorSantos, Luciana A.
dc.contributor.authorBolzani, Vanderlan da Silva [UNESP]
dc.contributor.authorNair, Muraleedharan G.
dc.contributor.institutionMichigan State University
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniv Calif Los Angeles
dc.date.accessioned2014-05-20T15:20:28Z
dc.date.available2014-05-20T15:20:28Z
dc.date.issued2007-04-04
dc.description.abstractPlants from Iryanthera genus have been traditionally used as food supplements by South American Indians. The MeOH extract of leaves of Iryanthera juruensis, one of the plants endemic to the Amazon region and consumed in Brazil, and the hexane extract from its seeds inhibited lipid peroxidation (LPO) and cyclooxygenase (COX-1 and -2)) enzymes in in vitro assays. Further analyses of these extracts yielded 5-deoxyflavones (1-5) from the leaf extract and sargachromenol (6), sargaquinoic acid (7), a novel juruenolic acid (8), omega-arylalkanoic acids (9a-c), and the lignan guaiacin (10) from the seed extract. Compounds 3-5 inhibited LPO by 86%, 77%, and 88% at 10 ppm, respectively, and compounds 6 and 9a-c showed inhibition at 76% and 78% at 100 ppm, respectively. However, compounds 7 and 8 were inactive and lignan 10 exhibited LPO inhibitory activity by 99% at 100 ppm compared to commercial antioxidants butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), and vitamin E. The flavones 1-5 also inhibited COX-1 and -2 enzymes by 50-65% at 100 ppm. Compound 6 showed high but nonselective inhibition of COX-1 and COX-2 enzymes, when compared to aspirin and Celebrex, a nonsteroidal anti-inflammatory drug (NSAID). Compounds 7 and 10 inhibited COX-1 by 60% and 65% and COX-2 by 37% and 18%, respectively, whereas compounds 8 and 9a-c showed little or no activity against these enzymes.en
dc.description.affiliationMichigan State Univ, Dept Hort, E Lansing, MI 48824 USA
dc.description.affiliationMichigan State Univ, Natl Food Safety & Toxicol Ctr, E Lansing, MI 48824 USA
dc.description.affiliationSão Paulo State Univ, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationUniv Calif Los Angeles, Ctr Human Nutr, Los Angeles, CA 90024 USA
dc.description.affiliationUnespSão Paulo State Univ, BR-14800900 Araraquara, SP, Brazil
dc.format.extent2569-2574
dc.identifierhttp://dx.doi.org/10.1021/jf063451x
dc.identifier.citationJournal of Agricultural and Food Chemistry. Washington: Amer Chemical Soc, v. 55, n. 7, p. 2569-2574, 2007.
dc.identifier.doi10.1021/jf063451x
dc.identifier.issn0021-8561
dc.identifier.lattes4702004904231248
dc.identifier.lattes4484083685251673
dc.identifier.orcid0000-0002-1516-7765
dc.identifier.urihttp://hdl.handle.net/11449/31763
dc.identifier.wosWOS:000245241700010
dc.language.isoeng
dc.publisherAmer Chemical Soc
dc.relation.ispartofJournal of Agricultural and Food Chemistry
dc.relation.ispartofjcr3.412
dc.relation.ispartofsjr1,269
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectIryanthera juruensispt
dc.subjectMyristicaceaept
dc.subjectlipid peroxidationpt
dc.subjectcyclooxygenasept
dc.subjectflavonept
dc.subjecttocotrienolpt
dc.subjectomega-arylalkanoic acidspt
dc.subjectlignanpt
dc.titleLipoperoxidation and cyclooxygenases 1 and 2 inhibitory compounds from Iryanthera juruensisen
dc.typeArtigo
dcterms.licensehttp://pubs.acs.org/paragonplus/copyright/jpa_form_a.pdf
dcterms.rightsHolderAmer Chemical Soc
dspace.entity.typePublication
unesp.author.lattes4702004904231248[1]
unesp.author.lattes4484083685251673
unesp.author.orcid0000-0002-1516-7765[1]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Orgânica - IQARpt

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