The present invention provides N-alkyl 2-(disubstituted)alkynyladenosine-5′-uronamides and derivatives thereof and pharmaceutical compositions containing the same that are selective agonists of A2A adenosine receptors (ARs). These compounds and compositions are useful as pharmaceutical agents.
本发明提供了N-烷基2-(二取代)炔基
腺苷-5'-尿
酰胺及其衍
生物和含有它们的药物组合物,这些化合物和组合物是A2A
腺苷受体(ARs)的选择性激动剂。这些化合物和组合物可用作药物剂。