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dc.contributor.authorQuintela, Jose´ M.-
dc.contributor.authorPeinador, Carlos-
dc.contributor.authorGonzález, Liliana-
dc.contributor.authorDevesa Giner, Isabel-
dc.contributor.authorFerrándiz, M. Luisa-
dc.contributor.authorAlcaraz, Maria Jose-
dc.contributor.authorRiguera, Ricardo-
dc.contributor.otherDepartamentos de la UMH::Bioquímica y Biología Moleculares_ES
dc.date.accessioned2025-01-24T17:20:14Z-
dc.date.available2025-01-24T17:20:14Z-
dc.date.created2002-11-
dc.identifier.citationBioorganic & Medicinal Chemistry 11 (2003) 863–868es_ES
dc.identifier.issn1464-3391-
dc.identifier.issn0968-0896-
dc.identifier.urihttps://hdl.handle.net/11000/35275-
dc.description.abstractThe synthesis of 6-dimethylamino 1H-pyrazolo[3,4-d]pyrimidines substituted at positions 1 and 4, and their effects on murine macrophage and human neutrophil functions are described. Several compounds and especially 4b–6b are potent inhibitors of PGE2 generation in murine macrophages. This action is related to a direct effect on COX-2 activity without affecting the enzyme expression. Some of these compounds also inhibited COX-1 and COX-2 in human monocytes and 4b showed selectivity for COX-2 inhibition.es_ES
dc.formatapplication/pdfes_ES
dc.format.extent6es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/closedAccesses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.otherCDU::5 - Ciencias puras y naturales::57 - Biología::576 - Biología celular y subcelular. Citologíaes_ES
dc.title6-Dimethylamino 1H-Pyrazolo[3,4-d]pyrimidine Derivatives as New Inhibitors ofInflammatory Mediators in Intact Cellses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://doi.org/10.1016/S0968-0896(02)00562-Xes_ES
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Artículos Bioquímica y Biología Molecular


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