Huang, Charles Q <br/><br/>
Design, synthesis, and SAR of 2-dialkylamino-4-arylpyrimidines as potent and selective corticotropin-releasing factor(1) (CRF(1)) receptor antagonists.  [electronic resource] 

 -  Bioorganic & medicinal chemistry letters  May 2004 
 - 2083-6 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0960-894X 
<br/><br/><label>Standard No.: </label>10.1016/j.bmcl.2004.02.053  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>CHO Cells<br/>Cricetinae<br/>Drug Design<br/>Pyrimidines--chemical synthesis<br/>Rats<br/>Receptors, Corticotropin-Releasing Hormone--antagonists & inhibitors<br/>Structure-Activity Relationship<br/>CRF Receptor, Type 1