131865-93-5Relevant academic research and scientific papers
SYNTHESIS OF 2-ARALKYLOXYADENOSINES, 2-ALKOXYADENOSINES, AND THEIR ANALOGS
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Page/Page column 16-17, (2008/06/13)
A practical process that solves many of the problems of prior art methods for the synthesis of 2-[2-(4-chlorophenyl)ethoxy]adenosine and its analogs is herein presented. This method provides advantages in cost, efficiency, and purity of the final product.
2-Aralkoxyadenosines: Potent and Selective Agonists at the Coronary Artery A2 Adenosine Receptor
Ueeda, Masayuki,Thompson, Robert D.,Arroyo, Luis H.,Olsson, Ray A.
, p. 1340 - 1344 (2007/10/02)
A Langendorff guines pig heart preparation served for the assay of agonist potency of a series of 26 2-aralkoxyadenosines at the A1 and A2 receptors of, respectively, the atrioventricular node (conduction block) and coronary arteries
