The thienopyridines class of drugs used as P2Y receptor antagonists plays a vital role in antiplatelet therapy. To further optimized this compound class, we designed and synthesized a series of amino acid prodrugs of 2-hydroxytetrahydrothienopyridine. All compounds were then evaluated for their inhibitory effect on ADP-induced platelet aggregation in rats and then ED and bleeding time of the most potent compounds were compared with commercial drugs. The results showed compound could be a potent and safe candidate for further research.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102589PMC
http://dx.doi.org/10.3390/molecules23051041DOI Listing

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