An Investigation Of The Sar In A Series Of N6-Cyclopentylethyl-Adenosine And N6-(2-Thienyl)Ethyl-Adenosine Agonists - Modification Of The 5'-Position Of Adenosine-Analogs Results In Dramatic Changes In Vasorelaxant Activity
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY(1991)
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