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Selective A1-adenosine receptor antagonists identified using yeast Saccharomyces cerevisiae functional assays
R M Campbell1, C Cartwright, W Chen
1Cadus Pharmaceutical Corporation, Tarrytown, NY 10591, USA.
Bioorganic & Medicinal Chemistry Letters
|September 7, 1999
Abstract:
Evaluation of a biased "library" of pyrrolo[2,3-d]pyrimidines using yeast-based functional assays expressing human A1- and A2a-adenosine receptors, led to the A1 selective antagonist 4b. A direct correlation between yeast functional activity and binding data was established. Practical compounds with polar residues at C-4 of the pyrrolopyrimidine system required H-bond donor functionality for high potency.