4.7 Review

Historical Lessons in Translational Medicine Cyclooxygenase Inhibition and P2Y12 Antagonism

Journal

CIRCULATION RESEARCH
Volume 112, Issue 1, Pages 174-194

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCRESAHA.111.300271

Keywords

aspirin; platelet; prostaglandin

Funding

  1. National Heart Lung and Blood Institute of the National Institutes of Health [HL062250, U54HL117798]

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The development of drugs that inhibit platelets has been driven by a combination of clinical insights, fundamental science, and sheer luck. The process has evolved as the days of stumbling on therapeutic gems, such as aspirin, have long passed and have been replaced by an arduous process in which a drug is designed to target a specific protein implicated in a well-characterized pathophysiological process, or so we would like to believe. The development of antiplatelet therapy illustrates the importance of understanding the mechanisms of disease and the pharmacology of the compounds we develop, coupled with careful clinical experimentation and observation and, yes, still, a fair bit of luck. (Circ Res. 2013; 112: 174-194.)

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