Brenton C Peters, Christopher J Fitzgerald
Index: Future Cardiol. 5(5) , 435-42, (2009)
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SCH 530348, a synthetic tricyclic 3-phenylpyridine, is an orally active fourth generation himbacine-based antagonist of the protease-activated receptor (PAR)-1, the primary receptor for thrombin on platelets in humans. SCH 530348 is the first in a new class of compounds that inhibit thrombin-mediated platelet aggregation without affecting the enzymatic activity of thrombin on fibrinogen. Preclinical and initial clinical studies have demonstrated this compound to be a highly potent inhibitor of thrombin-induced platelet activation, to have excellent oral bioavailability and to have a favorable safety profile. These data suggest that this compound has the potential to reduce the risk of ischemic events without significantly increasing the rate of bleeding. Two large Phase III clinical outcome trials are currently underway to evaluate the safety and efficacy of SCH 530348 for the management of acute coronary syndromes and the secondary prevention of atherothrombotic events.
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
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3-Phenylpyridine
CAS:1008-88-4 |
C11H9N |
|
Raman excitation profiles and excited state molecular config...
2000-04-01 [Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 56(5) , 855-75, (2000)] |
|
Surface-enhanced Raman spectroscopy studies of phenylpyridin...
[Surface Science 507 , 34-9, (2002)] |
|
Oxygenation of hydrocarbons by cytochrome P-450 model compou...
1983-11-01 [Proc. Natl. Acad. Sci. U. S. A. 80(22) , 7039-41, (1983)] |
|
1H, 13C and 15N nuclear magnetic resonance coordination shif...
2009-08-01 [Magn. Reson. Chem. 47(8) , 658-65, (2009)] |
|
Structure based development of phenylimidazole-derived inhib...
2008-08-28 [J. Med. Chem. 51 , 4968-77, (2008)] |
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