Article ID Journal Published Year Pages File Type
10598797 Bioorganic & Medicinal Chemistry Letters 2005 4 Pages PDF
Abstract
The structure-activity relationship investigation using 1 as a template led to the identification of a novel class of compounds as potent and selective antagonists of the A2A receptor. Compound 26 was identified to be the most potent A2A antagonist (Ki = 0.8 nM) with 100-fold selectivity over the A1 receptor.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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