Mou, Jiajia <br/><br/>
Design, synthesis and primary activity assay of bi- or tri-peptide analogues with the scaffold l-arginine as amino-peptidase N/CD13 inhibitors.  [electronic resource] 

 -  Bioorganic & medicinal chemistry  Jan 2010 
 - 887-95 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1464-3391 
<br/><br/><label>Standard No.: </label>10.1016/j.bmc.2009.11.036  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Arginine--chemistry<br/>CD13 Antigens--antagonists & inhibitors<br/>Crystallography, X-Ray<br/>Drug Design<br/>Enzyme Inhibitors--chemical synthesis<br/>Matrix Metalloproteinase Inhibitors<br/>Models, Molecular<br/>Molecular Conformation<br/>Oligopeptides--chemical synthesis<br/>Stereoisomerism<br/>Structure-Activity Relationship