scholarly journals Design and synthesis of N6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A3 adenosine receptor agonists

2009 ◽  
Vol 17 (23) ◽  
pp. 8003-8011 ◽  
Author(s):  
Won Jun Choi ◽  
Hyuk Woo Lee ◽  
Hea Ok Kim ◽  
Moshe Chinn ◽  
Zhan-Guo Gao ◽  
...  
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 ◽  
...  

2006 ◽  
Vol 16 (9) ◽  
pp. 2416-2418 ◽  
Author(s):  
Ran Zhu ◽  
Cynthia R. Frazier ◽  
Joel Linden ◽  
Timothy L. Macdonald

Sign in / Sign up

Export Citation Format

Share Document