Kang, Fu-An <br/><br/>
Parallel synthesis and SAR study of novel oxa-steroids as potent and selective progesterone receptor antagonists.  [electronic resource] 

 -  Bioorganic & medicinal chemistry letters  May 2007 
 - 2531-4 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.2007.02.013  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Cell Line, Tumor<br/>Chemistry, Pharmaceutical--methods<br/>Complement C3--metabolism<br/>Drug Design<br/>Female<br/>Humans<br/>Mifepristone--pharmacology<br/>Models, Chemical<br/>Protein Binding<br/>Rats<br/>Receptors, Glucocorticoid--antagonists & inhibitors<br/>Receptors, Progesterone--antagonists & inhibitors<br/>Steroids--chemistry<br/>Structure-Activity Relationship