Search for New Purine- and Ribose-Modified Adenosine Analogues as Selective Agonists and Antagonists at Adenosine Receptors

DOI: 10.1021/jm00007a014

Source and publish data:

Journal of Medicinal Chemistry p. 1174 - 1188 (1995)

Update date:2022-08-11

Topics:

Authors:

Siddiqi, Suhaib M.

Jacobson, Kenneth A.

Esker, John L.

Olah, Mark E.

Ji, Xiao-duo

et al. et al.

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Article abstract of DOI:10.1021/jm00007a014

The binding affinities at rat A₁, A_2a, and A₃ adenosine receptors of a wide range of derivatives of adenosine have been determined.Sites of modification include the purine moiety (1-, 3-, and 7-deaza; halo, alkyne, and ami

Full text of DOI:10.1021/jm00007a014

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