Kim, Mira <br/><br/>
Synthesis of proline analogues as potent and selective cathepsin S inhibitors.  [electronic resource] 

 -  Bioorganic & medicinal chemistry letters  Jun 2013 
 - 3140-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1464-3405 
<br/><br/><label>Standard No.: </label>10.1016/j.bmcl.2013.04.023  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Arthritis--chemically induced<br/>Benzoxazoles--chemical synthesis<br/>Cathepsin B--antagonists & inhibitors<br/>Cathepsin K--antagonists & inhibitors<br/>Cathepsins--antagonists & inhibitors<br/>Collagen--toxicity<br/>Disease Models, Animal<br/>Dogs<br/>Enzyme Inhibitors--chemical synthesis<br/>Half-Life<br/>Humans<br/>Mice<br/>Mice, Inbred ICR<br/>Microsomes--metabolism<br/>Proline--analogs & derivatives<br/>Protein Binding<br/>Rats<br/>Rats, Sprague-Dawley<br/>Stereoisomerism<br/>Structure-Activity Relationship