Organic & Biomolecular Chemistry · 2011 · 42 citations · 23 references
MedicineMedicinal ChemistryPharmacologyClinical PharmacologyDrug DesignHemostasisAntiplatelet TherapyAntithrombotic TherapyPlatelet AggregationPlatelet FunctionPlatelet PhysiologyStrokeAdenosine Diphosphate-induced Platelet AggregationAntiplatelet DrugsAqueous Solubility ImprovementAqueous Solubility OptimizationPlatelet Aggregation InhibitionPlatelet InhibitionPost-stroke Antithrombotic TherapyThrombosis Pathophysiology
Novel nitric oxide (NO) releasing derivatives (7a-7l) of 3-n-butylphthalide (NBP) were designed and synthesized. Compound 7e inhibited the adenosine diphosphate (ADP), thrombin (TH) and arachidonic acid (AA)-induced in vitro platelet aggregation, superior to NBP and aspirin, released moderate levels of NO, and improved aqueous solubility relative to NBP. Furthermore, 7e exhibited greater antithrombotic activity than NBP and aspirin in rats, and protected against collagen and adrenaline-induced thrombosis in mice. Therefore, NO-releasing NBP derivatives possessed potent antiplatelet aggregation and antithrombotic activity. Our findings may aid in the design of new therapeutic agents for the treatment of thrombosis-related ischemic stroke.
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The aggregation of blood platelets
G. V. R. Born, Michael Cross · The Journal of Physiology · 1963 · 2.1K citations
Medicine, Cell Biology, Hematology +12
Angela Casini, Andrea Scozzafava, Francesco Mincione et al. · Journal of Medicinal Chemistry · 2000 · 139 citations · Full text