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Feprazone is a non-steroidal anti-inflammatory drug (NSAID) and COX inhibitor that is 10-fold selective for COX-2 over COX-1.1 It reduces LPS-induced prostaglandin E2 (PGE2; Item No. 14010) production in bovine arterial endothelial cells (IC50 = 1 μM). Oral administration of feprazone (25-100 mg/kg) reduces vascular permeability, edema, and nociception in a rat model of adjuvant-induced arthritis.2
WARNING This product is not for human or veterinary use.
1. Effects of feprazone on cyclooxygenase in vitro. Yaoxue Xuebao 35(7), 481-483 (2000).
2. Pharmacological studies of 4-