Synergistic Inhibition of Both P2Y 1 and P2Y 12 Adenosine Diphosphate Receptors As Novel Approach to Rapidly Attenuate Platelet-Mediated Thrombosis
Author(s) -
Thomas Gremmel,
Ivan B. Yanachkov,
Milka Yanachkova,
George E. Wright,
Joseph M. Wider,
Vishnu Undyala,
Alan D. Michelson,
Andrew L. Frelinger,
Karin Przyklenk
Publication year - 2016
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.115.306885
Subject(s) - p2y12 , adenosine diphosphate , cangrelor , platelet , pharmacology , antithrombotic , adenosine , in vivo , p2y receptor , agonist , aspirin , purinergic receptor , platelet activation , bleeding time , chemistry , medicine , clopidogrel , receptor , biology , platelet aggregation , microbiology and biotechnology
Unlike currently approved adenosine diphosphate receptor antagonists, the new diadenosine tetraphosphate derivative GLS-409 targets not only P2Y12 but also the second human platelet adenosine diphosphate receptor P2Y1 and may, therefore, be a promising antiplatelet drug candidate. The current study is the first to investigate the in vivo antithrombotic effects of GLS-409.
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