Thrombin receptor (PAR-1) antagonists. Heterocycle-based peptidomimetics of the SFLLR agonist motif.
作者信息
Hoekstra W J, Hulshizer B L, McComsey D F, Andrade-Gordon P, Kauffman J A, Addo M F, Oksenberg D, Scarborough R M, Maryanoff B E
机构信息
R. W. Johnson Pharmaceutical Research Institute, Spring House, PA 19477, USA.
出版信息
Bioorg Med Chem Lett. 1998 Jul 7;8(13):1649-54. doi: 10.1016/s0960-894x(98)00292-3.
The thrombin receptor (PAR-1) is activated by alpha-thrombin to stimulate various cell types, including platelets, through the tethered-ligand sequence SFLLRN. A series of azole-based carboxamides, designed after SFLLR, were synthesized and evaluated in vitro. The compounds inhibited platelet aggregation induced by SFLLRN-NH2 or alpha-thrombin, and blocked the binding of [3H]-S-(p-F-Phe)-Har-L-Har-KY-NH2 to a CHRF membrane preparation of PAR-1. Oxazole 30 bound to PAR-1 with an IC50 of 1.6 microM, and gave IC50 values of 25 microM and 6.6 microM against alpha-thrombin- and SFLLRN-NH2-induced platelet aggregation, respectively.
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