PHOTOLABILE A-ADENOSINE RECEPTOR AGONISTS AS "CAGED" ELECTROPHYSIOLOGICAL PROBES.

Med Chem Res

Laboratory of Bioorganic Chemistry, National Institute of Diabetes, and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892.

Published: January 1991

5'-Ether derivatives of the potent adenosine agonist N-cyclopentyladenosine (CPA) were designed as "caged" ligands for the activation of A-adenosine receptors following photolysis. The synthesis involved a 2',3'-diol protection scheme using the acid labile ethoxymethynyl group. Generation of CPA was demonstrated chromatographically and in a bioassay measuring the inhibition of synaptic potentials in the rat hippocampus.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489149PMC

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