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dc.creatorCardinaletti, Claudia-
dc.creatorMattioli, Laura-
dc.creatorGhelfi, Francesca-
dc.creatorDel Bello, Fabio-
dc.creatorGianella, Mario-
dc.creatorBruzzone, Ariana-
dc.creatorParis, Hervé-
dc.creatorPerfumi, Marina-
dc.creatorPiergentili, Alessandro-
dc.creatorQuaglia, Wilma-
dc.creatorPigini, Maria-
dc.date2017-09-19T15:04:29Z-
dc.date2017-09-19T15:04:29Z-
dc.date2009-11-03-
dc.date2017-09-13T20:40:19Z-
dc.date.accessioned2019-04-29T15:48:54Z-
dc.date.available2019-04-29T15:48:54Z-
dc.date.issued2009-11-03-
dc.identifierCardinaletti, Claudia; Mattioli, Laura; Ghelfi, Francesca; Del Bello, Fabio; Gianella, Mario; et al.; Might adrenergic α2C-agonists/α2A-antagonists become novel therapeutic tools for pain treatment with morphine?; American Chemical Society; Journal of Medicinal Chemistry; 52; 22; 3-11-2009; 7319-7322-
dc.identifier0022-2623-
dc.identifierhttp://hdl.handle.net/11336/24561-
dc.identifier1520-4804-
dc.identifierCONICET Digital-
dc.identifierCONICET-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/302765-
dc.descriptionThe imidazoline nucleus linked in position 2 via an oxyethylene bridge to a phenyl ring carrying an ortho substituent of moderate steric bulk provided alpha(2)-adrenergic (AR) ligands endowed with significant alpha(2C)-agonism/alpha(2A)-antagonism. Similar behavior was displayed by cirazoline (12). For their positive morphine analgesia modulation (due to alpha(2C)-AR stimulation) and sedation overcoming (due to alpha(2A)-AR antagonism), 8 and 11 might be useful as adjuvant agents in the management of pain with morphine.-
dc.descriptionFil: Cardinaletti, Claudia. Università degli Studi di Camerino; Italia-
dc.descriptionFil: Mattioli, Laura. Università degli Studi di Camerino; Italia-
dc.descriptionFil: Ghelfi, Francesca. Università degli Studi di Camerino; Francia-
dc.descriptionFil: Del Bello, Fabio. Università degli Studi di Camerino; Francia-
dc.descriptionFil: Gianella, Mario. Università degli Studi di Camerino; Francia-
dc.descriptionFil: Bruzzone, Ariana. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina-
dc.descriptionFil: Paris, Hervé. Inserm; Francia-
dc.descriptionFil: Perfumi, Marina. Università degli Studi di Camerino; Francia-
dc.descriptionFil: Piergentili, Alessandro. Università degli Studi di Camerino; Francia-
dc.descriptionFil: Quaglia, Wilma. Università degli Studi di Camerino; Francia-
dc.descriptionFil: Pigini, Maria. Università degli Studi di Camerino; Francia-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherAmerican Chemical Society-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/abs/10.1021/jm901262f-
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/jm901262f-
dc.relationinfo:eu-repo/semantics/altIdentifier/pmid/19886609-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/-
dc.sourcereponame:CONICET Digital (CONICET)-
dc.sourceinstname:Consejo Nacional de Investigaciones Científicas y Técnicas-
dc.sourceinstacron:CONICET-
dc.subjectBioquímica y Biología Molecular-
dc.subjectMedicina Básica-
dc.subjectCIENCIAS MÉDICAS Y DE LA SALUD-
dc.subjectPatología-
dc.subjectMedicina Básica-
dc.subjectCIENCIAS MÉDICAS Y DE LA SALUD-
dc.titleMight adrenergic α2C-agonists/α2A-antagonists become novel therapeutic tools for pain treatment with morphine?-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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