167298-18-2Relevant articles and documents
The discovery and synthesis of highly potent, A(2a) receptor agonists
Keeling, Suzanne E.,Albinson, F. David,Ayres, Barry E.,Butchers, Peter R.,Chambers, C. Lynn,Cherry, Peter C.,Ellis, Frank,Ewan, George B.,Gregson, Michael,Knight, John,Mills, Keith,Ravenscroft, Paul,Reynolds, Linda H.,Sanjar, Shahin,Sheehan, Michael J.
, p. 403 - 406 (2000)
A series of N6,2-disubstituted adenosine analogues have been synthesized and their functional activity measured against A(2a) and A1 receptors. Examples of compounds with both a lipophilic N6-substituent and amino-functionalized 2-position were highly active at the A(2a) receptor on the human neutrophil. (C) 2000 Published by Elsevier Science Ltd. All rights reserved.