dc.creatorMatos, Maria João
dc.creatorPérez Cruz, Fernanda
dc.creatorVazquez Rodriguez, Saleta
dc.creatorUriarte, Eugenio
dc.creatorSantana, Lourdes
dc.creatorBorges, Fernanda
dc.creatorOlea Azar, Claudio
dc.date.accessioned2014-03-12T20:36:02Z
dc.date.accessioned2019-04-25T23:33:28Z
dc.date.available2014-03-12T20:36:02Z
dc.date.available2019-04-25T23:33:28Z
dc.date.created2014-03-12T20:36:02Z
dc.date.issued2013
dc.identifierBioorganic & Medicinal Chemistry 21 (2013) 3900–3906
dc.identifierdoi 10.1016/j.bmc.2013.04.015
dc.identifierhttp://repositorio.uchile.cl/handle/2250/121854
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/2426208
dc.description.abstractIn the present work we synthesized a series of hydroxy-3-arylcoumarins (compounds 1–9), some of them previously described as MAO-B selective inhibitors, with the aim of evaluating their antioxidant properties. Theoretical evaluation of ADME properties of all the derivatives was also carried out. From the ORAC-FL, ESR and CV data it was concluded that these derivatives are very good antioxidants, with a very interesting hydroxyl, DPPH and superoxide radicals scavenging profiles. In particular compound 9 is the most active and effective antioxidant of the series (ORAC-FL = 13.5, capacity of scavenging hydroxyl radicals = 100%, capacity of scavenging DPPH radicals = 65.9% and capacity of scavenging superoxide radicals = 71.5%). Kinetics profile for protection fluorescein probe against peroxyl radicals by addition of antioxidant molecule 9 was also performed. Therefore, it can operate as a potential candidate for preventing or minimizing the free radicals overproduction in oxidative-stress related diseases.
dc.languageen
dc.publisherElsevier
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.subject3-Arylcoumarins
dc.titleRemarkable antioxidant properties of a series of hydroxy-3-arylcoumarins
dc.typeArtículos de revistas


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