| 摘要 |
<p>A series of 15 N6-substituted 9-methyladenines have been assessed as antagonists of A¿2?-adenosine receptor-mediated stimulation of adenylate cyclase in membranes of human platelets and rat PC12 cells and of A1-adenosine receptor-mediated inhibition of adenylate cyclases in membranes of rat fat cells and as inhibitors of binding of N?6¿-R-[3H]-phenylisopropyladenosine to A¿1? adenosine receptors in rat brain membranes.</p> |
