Bioorganic and Medicinal Chemistry p. 81 - 90 (1996)
Update date:2022-08-30
Topics:
Barraclough, Paul
Bolofo, Mary L.
Giles, Heather
Gillam, Janet
Harris, C. John
Kelly, Michael G.
Leff, Paul
McNeill, Alan
Robertson, Alan D.
Stepney, Ray J.
Whittle, Brendan J. R.
The rationale for investigating conformationally restricted analogues of BW245C as DP-receptor ligands and the syntheses of three such racemic bicyclic imidazolidinone analogues are described. Compounds 7 (BW587C), 8 (BW480C85), and 9 (BW572C85) were found to be potent inhibitors of human platelet aggregation and selective DP-receptor agonists in washed platelet and jugular vein isolated tissue assays.
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