ChemInform Abstract: Synthesis and Biological Activity of a New Series of N6-Arylcarbamoyl, 2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-Carboxamido Derivatives of Adenosine-5′-N-ethyluronamide as A1 and A3 Adenosine Receptor Agonists.

ChemInform ◽  
2010 ◽  
Vol 29 (50) ◽  
pp. no-no
Author(s):  
P. G. BARALDI ◽  
ET AL. ET AL.
MedChemComm ◽  
2014 ◽  
Vol 5 (2) ◽  
pp. 192-196 ◽  
Author(s):  
Shane M. Devine ◽  
Lauren T. May ◽  
Peter J. Scammells

A series of N6-substituted 2-aminoadenosine-5′-N-methylcarboxamides were synthesized from the versatile intermediate, O6-(benzotriazol-1-yl)-2-amino-2′,3′-O-isopropylideneinosine-5′-N-methylcarboxamide (1) and evaluated as A3 adenosine receptor agonists.


ChemInform ◽  
2006 ◽  
Vol 37 (31) ◽  
Author(s):  
Ran Zhu ◽  
Cynthia R. Frazier ◽  
Joel Linden ◽  
Timothy L. Macdonald

Neoplasia ◽  
2001 ◽  
Vol 3 (2) ◽  
pp. 125-131 ◽  
Author(s):  
Sara Bar-Yehuda ◽  
Faina Barer ◽  
Lea Volisson ◽  
Pnina Fishman

2010 ◽  
Vol 18 (9) ◽  
pp. 3078-3087 ◽  
Author(s):  
Shane M. Devine ◽  
Alison Gregg ◽  
Heidi Figler ◽  
Kate McIntosh ◽  
Vijay Urmaliya ◽  
...  

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