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• W2000487734 abstract "5‘-(Alkylthio)-, 5‘-(methylseleno)-, and 5‘-(alkylamino)-substituted analogues of N6-cyclopentyladenosine (CPA) were synthesized in 30−50% overall yields. The affinities of these compounds for the adenosine A1 and A2A receptors were determined in rat brain membranes. The 5‘-substituted CPA analogues proved selective for the adenosine A1 receptors, displaying affinities in the nanomolar range. The compounds were also evaluated for their ability to stimulate [35S]GTPγS binding, also in rat brain membranes. The Ki values in receptor binding studies corresponded well to the EC50 values thus obtained. Intrinsic activities of the compounds were tested in vitro by determining the GTP shift in receptor binding studies as well as the maximal binding of [35S]GTPγS. It appeared that the 5‘-thio and 5‘-seleno derivatives in particular behaved as partial agonists." @default.
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• W2000487734 date "1998-01-01" @default.
• W2000487734 modified "2023-09-27" @default.
• W2000487734 title "5‘-Substituted Adenosine Analogs as New High-Affinity Partial Agonists for the Adenosine A₁ Receptor" @default.
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• W2000487734 doi "https://doi.org/10.1021/jm970508l" @default.
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