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Synthesis and antioxidant activity of long chain alkyl hydroxycinnamates

dc.contributor.authorMenezes, Jose C.J.M.D.S
dc.contributor.authorKamat, Shrivallabh P
dc.contributor.authorCavaleiro, Jose A.S.
dc.contributor.authorGaspar, Alexandra
dc.contributor.authorGarrido, Jorge
dc.contributor.authorBorges, Fernanda
dc.date.accessioned2019-03-20T12:05:24Z
dc.date.available2019-03-20T12:05:24Z
dc.date.issued2010
dc.description.abstractLong chain alkyl hydroxycinnamates (8e21) were synthesized from the corresponding half esters of malonic acid (5e7) and benzaldehyde derivatives by Knoevenagel condensation. The total antioxidant capacity of these hydroxycinnamyl esters was evaluated using DPPH and ABTS assays. The observed antioxidant activity was highest for esters of caffeic acid followed by sinapic esters and ferulic esters. The parameters for drug-likeness of these hydroxycinnamyl esters were also evaluated according to the Lipinski’s ‘rule-of-five’. All the ester derivatives were found to violate one of the Lipinski’s parameters (cLogP >5), even though they have been found to be soluble in protic solvents. The predictive topological polar surface area (TPSA) data allow concluding that they could have a good capacity for penetrating cell membranes. Therefore, one can propose these novel lipophilic compounds as potential antioxidants for tackling oxidative processes.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1016/j.ejmech.2010.12.016pt_PT
dc.identifier.issn0223-5234
dc.identifier.urihttp://hdl.handle.net/10400.22/13073
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S022352341000872Xpt_PT
dc.subjectAlkyl hydroxycinnamatespt_PT
dc.subjectAntioxidant activitypt_PT
dc.subjectCaffeic acidpt_PT
dc.subjectFerulic acidpt_PT
dc.subjectSinapic acidpt_PT
dc.subjectDrug-likeness propertiespt_PT
dc.titleSynthesis and antioxidant activity of long chain alkyl hydroxycinnamatespt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.titleEuropean Journal of Medicinal Chemistrypt_PT
person.familyNameGarrido
person.givenNameJorge
person.identifier.orcid0000-0001-8981-231X
person.identifier.scopus-author-id7202779733
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationf548e711-c68e-4c49-9471-9923c047116d
relation.isAuthorOfPublication.latestForDiscoveryf548e711-c68e-4c49-9471-9923c047116d

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