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dc.contributor.authorGarcía González, Celina Elena 
dc.contributor.authorEstévez-Sarmiento, Francisco
dc.contributor.authorSaid, Mercedes
dc.contributor.authorBrouard, Ignacio
dc.contributor.authorLeón, Francisco
dc.contributor.authorQuintana, José
dc.contributor.authorEstévez, Francisco
dc.date.accessioned2024-02-13T21:05:45Z
dc.date.available2024-02-13T21:05:45Z
dc.date.issued2017
dc.identifier.issn0968-0896
dc.identifier.urihttp://riull.ull.es/xmlui/handle/915/36261
dc.description.abstractFlavonoids are naturally occurring polyphenolic compounds and are among the most promising anticancer agents. A series of flavonols and their 3-methyl ether derivatives were synthesized and assessed for cytotoxicity. It was found that 3´-hydroxy-3,4´dimethoxyflavone (flavonoid 7a) displayed strong cytotoxicity against human SKMEL-1 melanoma cells and blocked tubulin polymerization, but had no significant cytotoxic effects against quiescent or proliferating human peripheral blood mononuclear cells. Our analyses showed that flavonoid 7a induces G2-M cell cycle arrest and apoptosis in melanoma cells which is associated with cytochrome c release and activation of both extrinsic and intrinsic apoptotic pathways of cell death.en
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.relation.ispartofseriesBioorganic and Medicinal Chemistry. 25(21), 2017, p. 6060-6070
dc.rightsLicencia Creative Commons (Reconocimiento-No comercial-Sin obras derivadas 4.0 Internacional)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es_ES
dc.title3,-Hydroxy-3,4,-dimethoxyflavone blocks tubulin polymerization and is a potent apoptotic inducer in human SK-MEL-1 melanoma cells
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/J.BMC.2017.09.043
dc.subject.keywordApoptosisen
dc.subject.keywordCaspasesen
dc.subject.keywordCytotoxicityen
dc.subject.keywordFlavonoidsen
dc.subject.keywordMelanomaen


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