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dc.contributor.authorÁlvarez Lozano, Raquel 
dc.contributor.authorAramburu Villar, Laura
dc.contributor.authorPuebla Ibáñez, María Pilar 
dc.contributor.authorCaballero Salvador, Esther 
dc.contributor.authorGonzález Díaz, Myriam 
dc.contributor.authorVicente, Alba
dc.contributor.authorMedarde Agustín, Manuel 
dc.contributor.authorPeláez Lamamie de C. Arroyo, Rafael 
dc.date.accessioned2018-09-06T11:25:15Z
dc.date.available2018-09-06T11:25:15Z
dc.date.issued2016
dc.identifier.urihttp://hdl.handle.net/10366/138233
dc.description.abstract[EN]Antimitotics binding at the colchicine site of tubulin are important antitumour and vascular disrupting agents. Pyridines and azines are privileged scaffolds in medicinal chemistry and in recent years many colchicine site ligands (CSL) have incorporated them into their structures with the aim of improving their pharmacokinetic and pharmacodynamics properties. CSL have been classified according to their chemical structures and the chemical structures of the pyridine and azine containing antimitotic compounds are described. The design principles behind the structural modifications and the achieved effect on the biological activity upon inclusion of these heterocycles are also discussed. Lessons from the achievements and failures have been extracted and future perspectives delineated.es_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivs 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectPharmaceutical chemistryes_ES
dc.subjectPyridinees_ES
dc.subjectDrug designes_ES
dc.subjectAzineses_ES
dc.subjectAntimitoticses_ES
dc.subjectTubulines_ES
dc.subjectColchicinees_ES
dc.subjectAntitumoures_ES
dc.titlePyridine Based Antitumour Compounds Acting at the Colchicine Sitees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.2174/092986732311160420104823
dc.relation.projectIDSA147U13es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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Attribution-NonCommercial-NoDerivs 4.0 International
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