Abstract
A novel series of P2Y(12) antagonists for development of drugs within the antiplatelet area is presented. The synthesis of the piperazinyl-pyridine urea derivatives and their structure-activity relationships (SAR) are described. Several compounds showed P2Y(12) antagonistic activities in the sub-micromolar range.
Copyright © 2011 Elsevier Ltd. All rights reserved.
MeSH terms
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Inhibitory Concentration 50
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Molecular Structure
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Piperazines / chemistry*
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Platelet Aggregation Inhibitors / chemical synthesis
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Platelet Aggregation Inhibitors / pharmacology
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Protein Binding / drug effects
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Purinergic Antagonists / chemical synthesis*
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Purinergic Antagonists / chemistry
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Purinergic Antagonists / pharmacology*
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Pyridines / chemistry*
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Receptors, Purinergic P2Y12 / metabolism
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Structure-Activity Relationship
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Urea / chemical synthesis*
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Urea / chemistry
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Urea / pharmacology*
Substances
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Piperazines
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Platelet Aggregation Inhibitors
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Purinergic Antagonists
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Pyridines
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Receptors, Purinergic P2Y12
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Urea