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Indobufen is a non-steroidal anti-inflammatory drug (NSAID) and COX inhibitor.1 It reduces thromboxane B2 (TXB2) but not prostaglandin E2 (PGE2) levels in LPS-stimulated isolated human monocytes. Indobufen inhibits collagen-induced ATP release and platelet aggregation in isolated human platelet-rich plasma (PRP).2 It reduces arachidonic acid-induced mortality in mice and rabbits (ED50s = 1.3 and 0.58 mg/kg, respectively).3
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1. Indobufen inhibits tissue factor in human monocytes through a thromboxane-
2. In vitro and ex vivo effects of indobufen on human platelet aggregation, the release reaction and thromboxane B2 production. Haemostasis 17(5), 293-300 (1987).
3. Inhibitory activity of indobufen (*) on platelet aggregation in vivo. Pharmacol. Res. Commun. 16(10), 979-985 (1984).