dc.creatorGavernet, Luciana
dc.creatorPalestro, Pablo Hernán
dc.creatorBruno Blanch, Luis Enrique
dc.date2012
dc.date2019-09-12T14:08:03Z
dc.identifierhttp://sedici.unlp.edu.ar/handle/10915/81055
dc.identifierissn:2090-7761
dc.descriptionQuinoxaline derivatives were studied as inhibitors of c-Met kinase, a receptor associated with high tumor grade and poor prognosis in a number of human cancers. In this paper we used docking methodologies to predict the binding conformation of a set of quinoxalines and to explain the differences of biological activities previously reported.
dc.descriptionFacultad de Ciencias Exactas
dc.formatapplication/pdf
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by/3.0/
dc.rightsCreative Commons Attribution 3.0 Unported (CC BY 3.0)
dc.subjectQuímica
dc.subjectQuinoxaline
dc.subjectc-Met kinase
dc.subjectinhibitors
dc.titleDocking Applied to the Study of Inhibitors of c-Met Kinase
dc.typeArticulo
dc.typeArticulo


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