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Bioorg Med Chem Lett ; 23(20): 5519-22, 2013 Oct 15.
Article in English | MEDLINE | ID: mdl-24012185

ABSTRACT

The aim of this study was to synthesize three nitro substituted chalcones and to evaluate their anti-inflammatory activity in the model of carrageenan induced edema in rats. The nitro chalcone were prepared by aldol condensation using of mechanical agitation and environmentally friendly solvents with 72-73% yields in approximately 2h. The three structures were evaluated on biological activity at dose of 200mg/kg and they showed anti-inflammatory protective effect by both oral and intraperitoneal administration, this effect was time dependent.


Subject(s)
Anti-Inflammatory Agents/chemical synthesis , Chalcone/chemistry , Administration, Oral , Animals , Anti-Inflammatory Agents/chemistry , Anti-Inflammatory Agents/therapeutic use , Area Under Curve , Chalcone/chemical synthesis , Chalcone/therapeutic use , Disease Models, Animal , Edema/chemically induced , Edema/drug therapy , ROC Curve , Rats
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