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Bioorg Med Chem Lett
; 10(4): 403-6, 2000 Feb 21.
Article
in English
| MEDLINE
| ID: mdl-10714510
ABSTRACT
A series of N6,2-disubstituted adenosine analogues have been synthesized and their functional activity measured against A2a and A1 receptors. Examples of compounds with both a lipophilic N6-substituent and amino-functionalized 2-position were highly active at the A2a receptor on the human neutrophil.