Tetrahydro-4-quinolinamines identified as novel P2Y1 receptor antagonists
Bioorganic & Medicinal Chemistry Letters(2008)
摘要
High-throughput screening of the GSK compound collection against the P2Y1 receptor identified a novel series of tetrahydro-4-quinolinamine antagonists. Optimal substitution around the piperidine group was pivotal for ensuring activity. An exemplar analog from this series was shown to inhibit platelet aggregation.
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关键词
P2Y1 receptor,Antagonist,Platelet aggregation,Thrombosis,Tetrahydro-4-quinolinamine
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