The development of a novel class of pharmacodynamic hybrids that inhibits COX-2 isoform is reported. These molecules display enhanced nitric oxide releasing properties due to the presence of an ionisable moiety. The in vivo analgesic/anti-inflammatory activity was maintained in relation to the parent compounds.

Improving the solubility of a new class of antiinflammatory pharmacodynamic hybrids, that release nitric oxide and inhibit cycloxygenase-2 isoenzyme / Biava M; Battilocchio C; Poce G; Alfonso S; Porretta GC; Schenone S; Calderone V; Martelli A; Testai L; Ghelardini C; Di Cesare Mannelli L; Sautebin L; Rossi A; Giordani A; Patrignani P; Anzini M; Consalvi S. - In: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY. - ISSN 0223-5234. - STAMPA. - 58:(2012), pp. 287-298. [10.1016/j.ejmech.2012.10.014]

Improving the solubility of a new class of antiinflammatory pharmacodynamic hybrids, that release nitric oxide and inhibit cycloxygenase-2 isoenzyme

Ghelardini C;Di Cesare Mannelli L;
2012

Abstract

The development of a novel class of pharmacodynamic hybrids that inhibits COX-2 isoform is reported. These molecules display enhanced nitric oxide releasing properties due to the presence of an ionisable moiety. The in vivo analgesic/anti-inflammatory activity was maintained in relation to the parent compounds.
2012
58
287
298
Biava M; Battilocchio C; Poce G; Alfonso S; Porretta GC; Schenone S; Calderone V; Martelli A; Testai L; Ghelardini C; Di Cesare Mannelli L; Sautebin L; Rossi A; Giordani A; Patrignani P; Anzini M; Consalvi S
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/960635
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