Novellino, Ettore <br/><br/>
2-(Benzimidazol-2-yl)quinoxalines: a novel class of selective antagonists at human A(1) and A(3) adenosine receptors designed by 3D database searching.  [electronic resource] 

 -  Journal of medicinal chemistry  Dec 2005 
 - 8253-60 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/jm050792d  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine--analogs & derivatives<br/>Adenosine A1 Receptor Antagonists<br/>Adenosine A3 Receptor Antagonists<br/>Adenosine-5'-(N-ethylcarboxamide)--metabolism<br/>Animals<br/>Benzimidazoles--chemical synthesis<br/>Binding, Competitive<br/>CHO Cells<br/>Cricetinae<br/>Databases, Factual<br/>Drug Design<br/>Humans<br/>Quinoxalines--chemical synthesis<br/>Receptor, Adenosine A1--chemistry<br/>Receptor, Adenosine A2A--metabolism<br/>Receptor, Adenosine A3--chemistry<br/>Xanthines--metabolism