Please use this identifier to cite or link to this item:
https://accedacris.ulpgc.es/handle/10553/48291
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Cachapa, Agostinho | en_US |
dc.contributor.author | Mederos, Alfredo | en_US |
dc.contributor.author | Gili, Pedro | en_US |
dc.contributor.author | Hernández-Molina, Rita | en_US |
dc.contributor.author | Domínguez, Sixto | en_US |
dc.contributor.author | Chinea, Erasmo | en_US |
dc.contributor.author | López Rodríguez, Matías | en_US |
dc.contributor.author | Feliz, Marta | en_US |
dc.contributor.author | Llusar, Rosa | en_US |
dc.contributor.author | Brito, Felipe | en_US |
dc.contributor.author | Ruiz de Galarreta, Carlos M. | en_US |
dc.contributor.author | Tarbraue, Carlos | en_US |
dc.contributor.author | Gallardo, Germán | en_US |
dc.contributor.other | Dominguez, Sixto | - |
dc.contributor.other | Gili, Pedro | - |
dc.contributor.other | Tabraue, Carlos | - |
dc.contributor.other | Llusar, Rosa | - |
dc.contributor.other | Feliz, Marta | - |
dc.contributor.other | Cachapa, Agostinho | - |
dc.date.accessioned | 2018-11-23T20:28:44Z | - |
dc.date.available | 2018-11-23T20:28:44Z | - |
dc.date.issued | 2006 | en_US |
dc.identifier.issn | 0277-5387 | en_US |
dc.identifier.uri | https://accedacris.ulpgc.es/handle/10553/48291 | - |
dc.description.abstract | Three new bis(dithiocarbamato)copper(II) complexes have been prepared and characterized by elemental analysis, UV-Vis, and IR spectroscopy: bis(4-piperidonedithiocarbamato)copper(II), [Cu(PdtC)(2)](2) (1), bis(piperidinedithiocarbamato)copper(II), [Cu(PpdtC)(2)](2) (2), and bis[(2-piperidinecarboxy)dithiocarbamato]copper(II), Cu(Ppidtc)(2) (3). The crystal structures of the complexes I and 2 have been determined using X-ray diffraction methods and they are dimeric. The coordination sphere of copper(II) ions is described as a distorted square-pyramid: the axial Cu-S bond distances 2.7 and 2.8 angstrom for 1 and 2, respectively, are longer than the equatorial Cu-S ones (2.3 angstrom). Complexes I and 2 are not soluble in water. In contrast, 3 is water soluble. The interaction of 31 the previously prepared bis[N-(dithiocarboxy)sarcosine]copper(II), Cu(Sdtc)(2) (4), and bis[(dicarboxymethyl)dithiocarbamato]copper(II), Cu(IdadtC)(2) (5), with nitric oxide in aqueous solution at pH 7.4 and 20 degrees C was spectrophotometrically studied and the experimental data were analysed by means of the SPEFO-LETAGROP and HYPERQUAD programs, respectively. The stability constants of the complexes CuL2(NO) and CuL2(NO)(2) [L = dithiocarbamate] were determined. The interaction of 1 and 2 with nitric oxide was theoretically studied by molecular mechanics methods. Complexes 3, 4 and 5 and the previously studied bis[(dihydroxyethyl)dithiocarbamato]copper(II), Cu(Deadtc)(2) (6), decrease the NO produced in vitro either by sodium nitroprusside (NPS) or by cultured murine macrophages J774 stimulated with lipopolysaccharide (LPS) and interferon-gamma (IFN gamma). Inducible nitric oxide synthase (iNOS) activity was determined by measuring the stable NO end product, nitrite, using a colorimetric assay. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Polyhedron | en_US |
dc.source | Polyhedron[ISSN 0277-5387],v. 25, p. 3366-3378 | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject | 2302 Bioquímica | en_US |
dc.subject.other | Transition-Metal Complexes | en_US |
dc.subject.other | High-Speed Computers | en_US |
dc.subject.other | Molecular-Structure | en_US |
dc.subject.other | Crystal-Structure | en_US |
dc.subject.other | Copper Diethyldithiocarbamate | en_US |
dc.subject.other | Dithiocarbamate Derivatives | en_US |
dc.subject.other | Equilibrium-Constants | en_US |
dc.subject.other | Graphical Methods | en_US |
dc.subject.other | Synthase | en_US |
dc.subject.other | N-(Dithiocarboxy)Sarcosine | en_US |
dc.title | Studies of the interaction between bis(dithiocarbamato)copper(II) complexes with nitric oxide in aqueous solution and biological applications | en_US |
dc.type | info:eu-repo/semantics/Article | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1016/j.poly.2006.06.008 | en_US |
dc.identifier.scopus | 33750913350 | - |
dc.identifier.isi | 000242681200018 | - |
dcterms.isPartOf | Polyhedron | - |
dcterms.source | Polyhedron[ISSN 0277-5387],v. 25 (17), p. 3366-3378 | - |
dc.contributor.authorscopusid | 8101121400 | - |
dc.contributor.authorscopusid | 7003304361 | - |
dc.contributor.authorscopusid | 7003511789 | - |
dc.contributor.authorscopusid | 55879919900 | - |
dc.contributor.authorscopusid | 7005494640 | - |
dc.contributor.authorscopusid | 6603461516 | - |
dc.contributor.authorscopusid | 7404254884 | - |
dc.contributor.authorscopusid | 35557809100 | - |
dc.contributor.authorscopusid | 56245992900 | - |
dc.contributor.authorscopusid | 7006816972 | - |
dc.contributor.authorscopusid | 7003806034 | - |
dc.contributor.authorscopusid | 6506833060 | - |
dc.contributor.authorscopusid | 6603046608 | - |
dc.description.lastpage | 3378 | en_US |
dc.description.firstpage | 3366 | en_US |
dc.relation.volume | 25 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.identifier.wos | WOS:000242681200018 | - |
dc.contributor.daisngid | 9487656 | - |
dc.contributor.daisngid | 30325918 | - |
dc.contributor.daisngid | 284725 | - |
dc.contributor.daisngid | 335862 | - |
dc.contributor.daisngid | 786601 | - |
dc.contributor.daisngid | 429324 | - |
dc.contributor.daisngid | 2434109 | - |
dc.contributor.daisngid | 282628 | - |
dc.contributor.daisngid | 2855225 | - |
dc.contributor.daisngid | 607998 | - |
dc.contributor.daisngid | 163559 | - |
dc.contributor.daisngid | 22361164 | - |
dc.contributor.daisngid | 906884 | - |
dc.contributor.daisngid | 1664323 | - |
dc.contributor.daisngid | 26052472 | - |
dc.contributor.daisngid | 30938142 | - |
dc.contributor.daisngid | 7801524 | - |
dc.identifier.investigatorRID | D-7601-2012 | - |
dc.identifier.investigatorRID | A-6682-2008 | - |
dc.identifier.investigatorRID | D-7126-2015 | - |
dc.identifier.investigatorRID | J-8241-2014 | - |
dc.identifier.investigatorRID | No ID | - |
dc.identifier.investigatorRID | No ID | - |
dc.description.numberofpages | 13 | en_US |
dc.utils.revision | Sí | en_US |
dc.contributor.wosstandard | WOS:Cachapa, A | - |
dc.contributor.wosstandard | WOS:Mederos, A | - |
dc.contributor.wosstandard | WOS:Gili, P | - |
dc.contributor.wosstandard | WOS:Hernandez-Molina, R | - |
dc.contributor.wosstandard | WOS:Dominguez, S | - |
dc.contributor.wosstandard | WOS:Chinea, E | - |
dc.contributor.wosstandard | WOS:Rodriguez, ML | - |
dc.contributor.wosstandard | WOS:Feliz, M | - |
dc.contributor.wosstandard | WOS:Llusar, R | - |
dc.contributor.wosstandard | WOS:Brito, F | - |
dc.contributor.wosstandard | WOS:de Galarreta, CMR | - |
dc.contributor.wosstandard | WOS:Tarbraue, C | - |
dc.contributor.wosstandard | WOS:Gallardo, G | - |
dc.date.coverdate | Diciembre 2006 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.jcr | 1,843 | - |
dc.description.jcrq | Q2 | - |
dc.description.scie | SCIE | - |
item.grantfulltext | none | - |
item.fulltext | Sin texto completo | - |
crisitem.author.dept | GIR IUIBS: Farmacología Molecular y Traslacional | - |
crisitem.author.dept | IU de Investigaciones Biomédicas y Sanitarias | - |
crisitem.author.dept | Departamento de Morfología | - |
crisitem.author.dept | GIR IATEXT: Didáctica, Aprendizaje y Motivación en Contextos Específicos | - |
crisitem.author.dept | IU de Análisis y Aplicaciones Textuales | - |
crisitem.author.dept | Departamento de Didácticas Específicas | - |
crisitem.author.orcid | 0000-0001-9920-8116 | - |
crisitem.author.orcid | 0000-0002-1516-1750 | - |
crisitem.author.parentorg | IU de Investigaciones Biomédicas y Sanitarias | - |
crisitem.author.parentorg | IU de Análisis y Aplicaciones Textuales | - |
crisitem.author.fullName | Tabraue Tarbay, Carlos | - |
crisitem.author.fullName | Gallardo Campos, Germán | - |
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