Hanessian, Stephen <br/><br/>
Structure-based organic synthesis of unnatural aeruginosin hybrids as potent inhibitors of thrombin.  [electronic resource] 

 -  Bioorganic & medicinal chemistry letters  Jun 2007 
 - 3480-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0960-894X 
<br/><br/><label>Standard No.: </label>10.1016/j.bmcl.2007.03.075  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amides--chemistry<br/>Antithrombins--chemical synthesis<br/>Crystallography, X-Ray<br/>Hydrophobic and Hydrophilic Interactions<br/>Indoles--chemistry<br/>Inhibitory Concentration 50<br/>Leucine--analogs & derivatives<br/>Models, Chemical<br/>Oligopeptides--chemical synthesis<br/>Structure-Activity Relationship<br/>Thrombin--antagonists & inhibitors