Baraldi, Pier Giovanni <br/><br/>
Design, synthesis, and biological evaluation of C9- and C2-substituted pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as new A2A and A3 adenosine receptors antagonists.  [electronic resource] 

 -  Journal of medicinal chemistry  Mar 2003 
 - 1229-41 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-2623 
<br/><br/><label>Standard No.: </label>10.1021/jm021023m  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Binding, Competitive<br/>Cricetinae<br/>Drug Design<br/>Humans<br/>Molecular Conformation<br/>Purinergic P1 Receptor Antagonists<br/>Pyrazoles--chemical synthesis<br/>Pyrimidines--chemical synthesis<br/>Radioligand Assay<br/>Receptor, Adenosine A2A<br/>Receptor, Adenosine A3<br/>Solubility<br/>Structure-Activity Relationship