scholarly journals Reply to ‘Highly selective A3 adenosine receptor agonists relieve chronic neuropathic pain’

2017 ◽  
Vol 27 (8) ◽  
pp. 969-969
Author(s):  
Rodolfo Couto Maia
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

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