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BW A868C is a hydantoin compound that is structurally related to the DP receptor agonist BW 245C.1,2 BW A868C antagonizes the prostaglandin D2 and BW 245C-induced activation of human platelet adenylate cyclase. It reverses the anti-aggregatory effects of DP receptor agonists in a dose-dependent manner. Likewise, BW A868C antagonizes the accumulation of cAMP in rabbit non-pigmented ciliary epithelial cells.3 It has virtually no effect on human TP, IP, EP1, EP2, and FP receptors. The Ki for BW A868C is approximately 1.7 nM.4
WARNING This product is not for human or veterinary use.
1. Hydantoin prostaglandin analogues, potent and selective inhibitors of platelet aggregation. J. Chem. Soc. Chem. Comm. 561-562 (1979).
2. The antagonism by BW A868C of PGD2 and BW245C activation of human platelet adenylate cyclase. Br. J. Pharmacol. 96(2), 301-306 (1989).
3. Identification of prostanoid receptors in rabbit non-
4. The classification of prostaglandin DP-