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Eur J Med Chem ; 37(4): 339-47, 2002 Apr.
Article in English | MEDLINE | ID: mdl-11960669

ABSTRACT

New 3-O-substituted benzyl pyridazinone compounds have been synthesised and evaluated for their cyclooxygenase inhibitory activity and COX-2 selectivity. Among the compounds synthesised, three compounds (11b-11d) have shown in vitro COX-2 selectivity. These compounds have been evaluated for their in vivo potential using carrageenan-induced rat paw edema assay. One compound (11b) showed 32% anti-inflammatory activity at 30 mgkg(-1) dose.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/chemical synthesis , Cyclooxygenase Inhibitors/chemical synthesis , Pyridazines/chemical synthesis , Animals , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Cell Line , Cyclooxygenase 1 , Cyclooxygenase 2 , Cyclooxygenase 2 Inhibitors , Cyclooxygenase Inhibitors/chemistry , Cyclooxygenase Inhibitors/pharmacology , Female , Isoenzymes/antagonists & inhibitors , Isoenzymes/chemistry , Male , Membrane Proteins , Prostaglandin-Endoperoxide Synthases/chemistry , Pyridazines/chemistry , Pyridazines/pharmacology , Rats , Rats, Wistar
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