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dc.contributor.author | Carrión, M. Dora | |
dc.contributor.author | López Cara, Luisa C. | |
dc.contributor.author | Camacho, M. Encarnación | |
dc.contributor.author | Tapias Molina, Victor | |
dc.contributor.author | Escames, Germaine | |
dc.contributor.author | Acuña Castroviejo, Darío | |
dc.contributor.author | Espinosa, Antonio | |
dc.contributor.author | Gallo, Miguel A. | |
dc.contributor.author | Entrena, Antonio | |
dc.date.accessioned | 2024-01-01T20:54:55Z | |
dc.date.available | 2024-01-01T20:54:55Z | |
dc.date.issued | 2008 | |
dc.identifier.citation | European Journal of Medicinal Chemistry, Noviembre 2008, vol. 43, n. 11, p. 2579-2591 | es |
dc.identifier.issn | 0223-5234 | es |
dc.identifier.uri | https://uvadoc.uva.es/handle/10324/63871 | |
dc.description | Producción Científica | es |
dc.description.abstract | We 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.mimetype | application/pdf | es |
dc.language.iso | eng | es |
dc.rights.accessRights | info:eu-repo/semantics/embargoedAccess | es |
dc.title | Pyrazoles and pyrazolines as neural and inducible nitric oxide synthase (nNOS and iNOS) potential inhibitors (III) | es |
dc.type | info:eu-repo/semantics/article | es |
dc.identifier.doi | 10.1016/j.ejmech.2008.01.014 | es |
dc.identifier.publicationfirstpage | 2579 | es |
dc.identifier.publicationissue | 11 | es |
dc.identifier.publicationlastpage | 2591 | es |
dc.identifier.publicationtitle | European Journal of Medicinal Chemistry | es |
dc.identifier.publicationvolume | 43 | es |
dc.peerreviewed | SI | es |
dc.description.project | This 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.hasVersion | info:eu-repo/semantics/publishedVersion | es |