Ngatcha, Béatrice Tchédam <br/><br/>
3Beta-alkyl-androsterones as inhibitors of type 3 17beta-hydroxysteroid dehydrogenase: inhibitory potency in intact cells, selectivity towards isoforms 1, 2, 5 and 7, binding affinity for steroid receptors, and proliferative/antiproliferative activities on AR+ and ER+ cell lines.  [electronic resource] 

 -  Molecular and cellular endocrinology  Mar 2006 
 - 225-32 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0303-7207 
<br/><br/><label>Standard No.: </label>10.1016/j.mce.2005.10.023  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>17-Hydroxysteroid Dehydrogenases--antagonists & inhibitors<br/>Androsterone--analogs & derivatives<br/>Cell Proliferation--drug effects<br/>Enzyme Inhibitors--chemical synthesis<br/>Humans<br/>Isoenzymes--antagonists & inhibitors<br/>Receptors, Steroid--drug effects