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dc.contributor.authorPadrón Carrillo, José Manuel 
dc.contributor.authorLuque Agudo, Verónica
dc.contributor.authorAlbarrán Velo, Jesús
dc.contributor.authorLight, Mark. E.
dc.contributor.authorRomán, Emilio
dc.contributor.authorSerrano, José A.
dc.contributor.authorGil, Victoria
dc.contributor.otherQuímica Orgánica
dc.contributor.otherBioLab, Instituto Universitario de Bio-Orgánica Antonio González
dc.date.accessioned2024-01-15T21:09:23Z
dc.date.available2024-01-15T21:09:23Z
dc.date.issued2019
dc.identifier.issn0045-2068
dc.identifier.issn1090-2120
dc.identifier.urihttp://riull.ull.es/xmlui/handle/915/35361
dc.description.abstract3‐nitro‐2H‐chromenes and derivatives are compounds with diverse biological activity, among them, new 2‐glyco‐3‐nitro‐2H‐chromenes have been prepared by one‐pot oxa‐Michael‐Henry‐ dehydration reactions between carbohydrate‐derived nitroalkenes and several salicylaldehydes, using a minimal amount of solvent and DBU as catalyst. The antiproliferative activity of these new compounds has been evaluated against a panel of six human solid tumor cell lines, and compared to pharmacological reference compounds, finding that their activities are in the low micromolar range and that some of them are more effective than the standards.en
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.relation.ispartofseriesBioorganic Chemistry 2019, Volume 87, Pages 112-116
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.titleSynthesis and antiproliferative activity of new 2-glyco-3-nitro-2H-chromenesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.bioorg.2019.03.016
dc.subject.keyword3‐nitro‐2H‐chromenesen
dc.subject.keywordantiproliferative activityen
dc.subject.keywordstructure‐activity relationshipen
dc.subject.keywordcarbohydratesen


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