2-Substitution of N(6)-Benzyladenosine-5′-uronamides Enhances Selectivity for A(3) Adenosine Receptors

Míreanna Comhchosúla

• Structure–Activity Relationships of N(6)-Benzyladenosine-5′-uronamides as A(3)-Selective Adenosine Agonists()
  le: Gallo-Rodriguez, Carola, et al.
  Foilsithe: (1994)
• Design and Synthesis of N(6)-Substituted-4′-thioadenosine-5′-uronamides As Potent and Selective Human A(3) Adenosine Receptor Agonists
  le: Choi, Won Jun, et al.
  Foilsithe: (2009)
• Identification of an Adenosine Receptor Domain Specifically Involved in Binding of 5′-Substituted Adenosine Agonists
  le: Olah, Mark E., et al.
  Foilsithe: (1994)
• A(3)-adenosine receptors: design of selective ligands and therapeutic prospects
  le: Jacobson, Kenneth A., et al.
  Foilsithe: (1995)
• Structure–Activity Relationships of 9-Alkyladenine and Ribose-Modified Adenosine Derivatives at Rat A(3) Adenosine Receptors
  le: Jacobson, Kenneth A., et al.
  Foilsithe: (1995)