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dc.creatorBurguete, A. (Asunción)
dc.creatorPontiki, E. (Eleni)
dc.creatorHadjipavlou-Litina, D. (Dimitra)
dc.creatorAncizu, S. (Saioa)
dc.creatorRaquel
dc.creatorSolano, B. (Beatriz)
dc.creatorMoreno-de-Viguri, E. (Elsa)
dc.creatorTorres, E. (Enrique)
dc.creatorPérez-Silanes, S. (Silvia)
dc.creatorAldana, I. (Ignacio)
dc.creatorMonge, A. (Antonio)
dc.date.accessioned2011-06-21T07:23:02Z-
dc.date.available2011-06-21T07:23:02Z-
dc.date.issued2011-
dc.identifier.citationBurguete A, Pontiki E, Hadjipavlou-Litina D, Ancizu S, Villar R, Solano B, et al. Synthesis and biological evaluation of new quinoxaline derivatives as antioxidant and anti-inflammatory agents. Chem Biol Drug Des 2011 Apr;77(4):255-267.es_ES
dc.identifier.issn1747-0277-
dc.identifier.urihttps://hdl.handle.net/10171/18591-
dc.description.abstractWe report the synthesis, anti-inflammatory and antioxidant activities of novel quinoxaline and quinoxaline 1,4-di-N-oxide derivatives. Microwave assisted methods have been used in order to optimize reaction times and to improve the yields. The tested compounds presented important scavenging activities and promising in vitro inhibition of soybean lipoxygenase. Two of the best lipoxygenase inhibitors (compounds 7b and 8f) were evaluated as in vivo anti-inflammatory agents using the carrageenin-induced edema model. One of them (compound 7b) showed important in vivo anti-inflammatory effect (41%) similar to that of indomethacin (47%) used as the reference drug.es_ES
dc.language.isoenges_ES
dc.publisherWiley-Blackwelles_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectQuinoxaline derivativeses_ES
dc.subjectAnti-inflammatory agentses_ES
dc.subject1,4-di-N-oxide derivativeses_ES
dc.subjectSoybean lipoxygenasees_ES
dc.titleSynthesis and biological evaluation of new quinoxaline derivatives as antioxidant and anti-inflammatory agentses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doihttp://dx.doi.org/10.1111/j.1747-0285.2011.01076.xes_ES

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