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dc.contributor.authorCarrión, M. Dora
dc.contributor.authorLópez Cara, Luisa C.
dc.contributor.authorCamacho, M. Encarnación
dc.contributor.authorTapias Molina, Victor 
dc.contributor.authorEscames, Germaine
dc.contributor.authorAcuña Castroviejo, Darío
dc.contributor.authorEspinosa, Antonio
dc.contributor.authorGallo, Miguel A.
dc.contributor.authorEntrena, Antonio
dc.date.accessioned2024-01-01T20:54:55Z
dc.date.available2024-01-01T20:54:55Z
dc.date.issued2008
dc.identifier.citationEuropean Journal of Medicinal Chemistry, Noviembre 2008, vol. 43, n. 11, p. 2579-2591es
dc.identifier.issn0223-5234es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/63871
dc.descriptionProducción Científicaes
dc.description.abstractWe have previously described a series of 4,5-dihydro-1H-pyrazole as moderately potent nNOS inhibitors. As a follow up of these studies, we report here the preparation and the preliminary evaluation of a series of 1-alkyl-3-benzoyl-4,5-dihydro-1H-pyrazole and 1-alkyl-3-benzoyl-1H-pyrazole as potential inhibitors of both neuronal and inducible nitric oxide synthases (nNOS and iNOS). None of the reported compounds exhibited significant iNOS or nNOS inhibition, although the 1-benzyl-3-(2-amino-5-chlorobenzoyl)-1H-pyrazole-5-carboxylic acid ethyl ester derivative (10l), which shows an inhibition of 50% versus iNOS at a 1mM final concentration and no activity against nNOS, is potentially amenable of further optimization. The reasons for the inactivity of the reported series are discussed on the basis of docking studies.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.rights.accessRightsinfo:eu-repo/semantics/embargoedAccesses
dc.titlePyrazoles and pyrazolines as neural and inducible nitric oxide synthase (nNOS and iNOS) potential inhibitors (III)es
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1016/j.ejmech.2008.01.014es
dc.identifier.publicationfirstpage2579es
dc.identifier.publicationissue11es
dc.identifier.publicationlastpage2591es
dc.identifier.publicationtitleEuropean Journal of Medicinal Chemistryes
dc.identifier.publicationvolume43es
dc.peerreviewedSIes
dc.description.projectThis work was partially supported by grants from the Ministerio de Ciencia y Tecnología (SAF2005-07991-C02-01 and SAF2005-07991-C02-02) and from the Junta de Andalucía (P06-CTS-01941).
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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