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Xanthenedione derivatives, new promising antioxidant and acetylcholinesterase inhibitor agents

dc.contributor.authorSeca, Ana M. L.
dc.contributor.authorLeal, Stephanie B.
dc.contributor.authorPinto, Diana C. G. A.
dc.contributor.authorBarreto, Maria do Carmo
dc.contributor.authorSilva, Artur M. S.
dc.date.accessioned2014-10-14T11:44:21Z
dc.date.available2014-10-14T11:44:21Z
dc.date.issued2014-06
dc.date.updated2014-09-22T10:07:47Z
dc.description.abstractNatural and synthetic xanthone derivatives are well-known for their ability to act as antioxidants and/or enzyme inhibitors. This paper aims to present a successful synthetic methodology towards xanthenedione derivatives and the study of their aromatization to xanthones. Additionally their ability to reduce Fe(III), to scavenge DPPH radicals and to inhibit AChE was evaluated. The results demonstrated that xanthenedione derivative 5e, bearing a catechol unit, showed higher reduction capacity than BHT and similar to quercetin, strong DPPH scavenging activity (EC50 = 3.79 ± 0.06 μM) and it was also showed to be a potent AChEI (IC50 = 31.0 ± 0.09 μM) when compared to galantamine (IC50 = 211.8 ± 9.5 μM).en
dc.identifier.citationSeca, Ana; Leal, Stephanie; Pinto, Diana; Barreto, Maria; Silva, Artur (2014). "Xanthenedione derivatives, new promising antioxidant and acetylcholinesterase inhibitor agents", Molecules, 19(6), 8317-8333. Doi: 10.3390/molecules19068317.en
dc.identifier.doi10.3390/molecules19068317
dc.identifier.issn1420-3049
dc.identifier.urihttp://hdl.handle.net/10400.3/3182
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherMDPIpor
dc.relation.publisherversionhttp://www.mdpi.com/1420-3049/19/6/8317por
dc.subjectXanthene-1,9(2H)-dionespor
dc.subjectScavenging Activityen
dc.subjectReduction Poweren
dc.subjectAcetylcholinesterase Inhibitorsen
dc.subjectXanthonespor
dc.subject3-cinnamoyl-5-hydroxy-2-styrylchromonespor
dc.titleXanthenedione derivatives, new promising antioxidant and acetylcholinesterase inhibitor agentsen
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceBasel, Switzerlanden
oaire.citation.endPage8333por
oaire.citation.issue(6)por
oaire.citation.startPage8317por
oaire.citation.titleMoleculesen
oaire.citation.volume19por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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