Design, synthesis and evaluation of N6-substituted 2-aminoadenosine-5′-N-methylcarboxamides as A3 adenosine receptor agonists

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.

RSC Advances ◽  
2016 ◽  
Vol 6 (14) ◽  
pp. 11233-11239 ◽  
Author(s):  
Amarendra Panda ◽  
Suresh Satpati ◽  
Anshuman Dixit ◽  
Shantanu Pal

A series of homologated-apio adenosine derivatives including homologated-apio IB-MECA and Cl-IB-MECA have been designed and synthesized successfully. The molecular modelling and docking studies of the compounds have been explored as A3AR agonists.


MedChemComm ◽  
2015 ◽  
Vol 6 (4) ◽  
pp. 555-563 ◽  
Author(s):  
Dilip K. Tosh ◽  
Silvia Paoletta ◽  
Zhoumou Chen ◽  
Steven Crane ◽  
John Lloyd ◽  
...  

C2-phenylethynyl (dark green) and C2-phenyl-triazolyl (light green) nucleosides in the A3AR.


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

2018 ◽  
Vol 61 (1) ◽  
pp. 305-318 ◽  
Author(s):  
Riccardo Petrelli ◽  
Mirko Scortichini ◽  
Carmela Belardo ◽  
Serena Boccella ◽  
Livio Luongo ◽  
...  

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