scholarly journals N6-Substituted 5′-N-Methylcarbamoyl-4′-selenoadenosines as Potent and Selective A3 Adenosine Receptor Agonists with Unusual Sugar Puckering and Nucleobase Orientation

2017 ◽  
Vol 60 (8) ◽  
pp. 3422-3437 ◽  
Author(s):  
Jinha Yu ◽  
Long Xuan Zhao ◽  
Jongmi Park ◽  
Hyuk Woo Lee ◽  
Pramod K. Sahu ◽  
...  
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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