Li, A H <br/><br/>
Synthesis, CoMFA analysis, and receptor docking of 3,5-diacyl-2, 4-dialkylpyridine derivatives as selective A3 adenosine receptor antagonists.  [electronic resource] 

 -  Journal of medicinal chemistry  Feb 1999 
 - 706-21 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0022-2623 
<br/><br/><label>Standard No.: </label>10.1021/jm980550w  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Binding Sites<br/>Binding, Competitive<br/>Bridged Bicyclo Compounds, Heterocyclic--chemical synthesis<br/>CHO Cells<br/>Cell Line<br/>Cerebral Cortex--metabolism<br/>Cricetinae<br/>Humans<br/>In Vitro Techniques<br/>Ligands<br/>Mice<br/>Models, Molecular<br/>Neostriatum--metabolism<br/>Purinergic P1 Receptor Agonists<br/>Radioligand Assay<br/>Rats<br/>Receptor, Adenosine A3<br/>Receptors, Purinergic P1--metabolism<br/>Recombinant Proteins--agonists<br/>Structure-Activity Relationship