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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:J Med Chem
Hauptverfasser: 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
Sprache:Inglês
Veröffentlicht: 1994
Schlagworte:
Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4474279/
https://ncbi.nlm.nih.gov/pubmed/8126704
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge