Add time:08/28/2019         Source:sciencedirect.com

A number of 2-aminothiazoles (2a–e) and their amide derivatives (4–10) were prepared. The 2-aminothiazoles themselves were tested as allosteric enhancers of agonist binding to human adenosine A1 receptors. In a variety of experimental set-ups the compounds did not show any such effect, in contrast to earlier findings by another research group. Subsequently the 2-aminothiazoles were used as intermediates in the synthesis of a number of amide derivatives of either aromatic (4–6) or aliphatic nature (7–10). Some of the compounds emerged as moderately active antagonists on human adenosine A1 and/or A2A receptors with lower or negligible potency at adenosine A3 receptors.

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