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Authordc.contributor.authorMatos, María 
Authordc.contributor.authorMura Mardones, Francisco 
Authordc.contributor.authorVázquez Rodríguez, Saleta 
Authordc.contributor.authorBorges, Fernanda 
Authordc.contributor.authorSantana, Lourdes 
Authordc.contributor.authorUriarte, Eugenio 
Authordc.contributor.authorOlea Azar, Claudio 
Admission datedc.date.accessioned2015-08-04T18:22:10Z
Available datedc.date.available2015-08-04T18:22:10Z
Publication datedc.date.issued2015
Cita de ítemdc.identifier.citationMolecules 2015, 20, 3290-3308en_US
Identifierdc.identifier.issn1420-3049
Identifierdc.identifier.otherDOI: 10.3390/molecules20023290
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/132345
General notedc.descriptionArtículo de publicación ISIen_US
Abstractdc.description.abstractIn the present work we synthesized a selected series of hydroxylated 3-phenylcoumarins 5–8, with the aim of evaluating in detail their antioxidant properties. From an in depth study of the antioxidant capacity data (ORAC-FL, ESR, CV and ROS inhibition) it was concluded that these derivatives are very good antioxidants, with very interesting profiles in all the performed assays. The study of the effect of the number and position of the hydroxyl groups on the antioxidant activity was the principal aim of this study. In particular, 7-hydroxy-3-(3'-hydroxy)phenylcoumarin (8) proved to be the most active and effective antioxidant of the selected series in four of the performed assays (ORAC-FL = 11.8, capacity of scavenging hydroxyl radicals = 54%, Trolox index = 2.33 and AI30 index = 0.18). However, the presence of two hydroxyl groups on this molecule did not increase greatly the activity profile. Theoretical evaluation of ADME properties of all the derivatives was also carried out. All the compounds can act as potential candidates for preventing or minimizing the free radical overproduction in oxidative-stress related diseases. These preliminary findings encourage us to perform a future structural optimization of this family of compounds.en_US
Patrocinadordc.description.sponsorshipFONDECYT 1110029 1090078 CONICYT Spanish researchers personal founds University of Santiago de Compostela Fundacao para a Ciencia e Tecnologia (FCT) Pest/C-QUI/UI0081/2013 Fundacao para a Ciencia e Tecnologia (FCT) POPH (Programa Operacional Potencial Humano) QREN (Quadro de Referencia Estrategica Nacional) SFRH/BPD/95345/2013 Universidade de Porto postdoctoral grant NORTE-07-0124-FEDER-000065 21120376
Lenguagedc.language.isoenen_US
Publisherdc.publisherMDPI AGen_US
Type of licensedc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Keywordsdc.subjectHydroxylated 3-phenylcoumarinsen_US
Keywordsdc.subjectAntioxidant assaysen_US
Keywordsdc.subjectElectrochemical studyen_US
Keywordsdc.subjectInhibition of ROSen_US
Keywordsdc.subjectESRen_US
Keywordsdc.subjectADME propertiesen_US
Títulodc.titleStudy of Coumarin-Resveratrol Hybrids as Potent Antioxidant Compoundsen_US
Document typedc.typeArtículo de revista


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Atribución-NoComercial-SinDerivadas 3.0 Chile
Except where otherwise noted, this item's license is described as Atribución-NoComercial-SinDerivadas 3.0 Chile