Structure–Activity Relationships of N(6)-Benzyladenosine-5′-uronamides as A(3)-Selective Adenosine Agonists()

Adenosine analogues modified at the 5′-position as uronamides and/or as N(6)-benzyl derivatives were synthesized. These derivatives were examined for affinity in radioligand binding assays at the newly discovered rat brain A(3) adenosine receptor and at rat brain A(1) and A(2a) receptors. 5′-Uronami...

Full description

Saved in:
Bibliographic Details
Published in:J Med Chem
Main Authors: Gallo-Rodriguez, Carola, Ji, Xiao-duo, Melman, Neli, Siegman, Barry D., Sanders, Lawrence H., Orlina, Jeraldine, Fischer, Bilha, Pu, Quanlong, Olah, Mark E., van Galen, Philip J. M., Stiles, Gary L., Jacobson, Kenneth A.
Format: Artigo
Language:Inglês
Published: 1994
Subjects:
Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4474279/
https://ncbi.nlm.nih.gov/pubmed/8126704
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items