Department of Pharmacology, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
PLoS One. 2013 Jun 11;8(6):e65528. doi: 10.1371/journal.pone.0065528. Print 2013.
Protease activated receptor-4 (PAR4) is one of the thrombin receptors on human platelets and is a potential target for the management of thrombotic disorders. We sought to develop potent, selective, and novel PAR4 antagonists to test the role of PAR4 in thrombosis and hemostasis. Development of an expedient three-step synthetic route to access a novel series of indole-based PAR4 antagonists also necessitated the development of a platelet based high-throughput screening assay. Screening and subsequent structure activity relationship analysis yielded several selective PAR4 antagonists as well as possible new scaffolds for future antagonist development.
蛋白酶激活受体 4(PAR4)是人血小板上的凝血酶受体之一,是治疗血栓性疾病的潜在靶点。我们试图开发强效、选择性和新型的 PAR4 拮抗剂,以测试 PAR4 在血栓形成和止血中的作用。为了开发一种便捷的三步合成路线来获得一系列新型吲哚基 PAR4 拮抗剂,也需要开发一种基于血小板的高通量筛选测定法。筛选和随后的构效关系分析得到了几种选择性 PAR4 拮抗剂以及未来拮抗剂开发的可能新骨架。