Publication | Open Access
Lipophilic Modifications to Dinucleoside Polyphosphates and Nucleotides that Confer Antagonist Properties at the Platelet P2Y<sub>12</sub> Receptor
38
Citations
32
References
2008
Year
Adp-mediated Platelet AggregationPharmacotherapyConfer Antagonist PropertiesThrombosisMolecular PharmacologyMedicinal ChemistryPlatelet AntagonistDinucleoside PolyphosphatesPlatelet P2y12 ReceptorsBiochemistryG Protein-coupled ReceptorAdenosine Monophosphate DerivativeReceptor (Biochemistry)Vascular BiologyLipophilic ModificationsPharmacologyPlatelet ActivationThrombopoiesisPlatelet Aggregation InhibitorsSignal TransductionBlood PlateletNatural SciencesMedicineDrug Discovery
Platelet P2Y12 receptors play a central role in the regulation of platelet function and inhibition of this receptor by treatment with drugs such as clopidogrel results in a reduction of atherothrombotic events. We discovered that modification of natural and synthetic dinucleoside polyphosphates and nucleotides with lipophilic substituents on the ribose and base conferred P2Y12 receptor antagonist properties to these molecules producing potent inhibitors of ADP-mediated platelet aggregation. We describe methods for the preparation of these functionalized dinucleoside polyphosphates and nucleotides and report their associated activities. By analysis of these results and by deconstruction of the necessary structural elements through selected syntheses, we prepared a series of highly functionalized nucleotides, resulting in the selection of an adenosine monophosphate derivative (62) for further clinical development.
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