
Bioorganic and Medicinal Chemistry Letters p. 3499 - 3504 (1998)
Update date:2022-08-03
Topics:
Xue, Chu-Biao
Roderick, John
Mousa, Shaker
Olson, Richard E.
DeGrado, William F.
Despite the excellent in vitro potency of a series of benzamide glycoprotein IIb/IIIa antagonists, which have been reported previously, poor in vivo potency in the inhibition of platelet aggregation was observed when the most potent inhibitor XU057 was dosed intravenously to dogs. In this communication, we report that replacement of the benzamide in XU057 with an isoxazolecarboxamide resulted in significant improvement in in vivo potency. More importantly, the analogue XU065 showed an excellent oral antiplatelet effect in dogs.
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