De Lucca, G V <br/><br/>
De novo design and discovery of cyclic HIV protease inhibitors capable of displacing the active-site structural water molecule.  [electronic resource] 

 -  Pharmaceutical biotechnology  1998 
 - 257-84 p.  digital 
<br/><br/> Publication Type: Journal Article; Review 
<br/><br/><label>ISSN: </label>1078-0467 
<br/><br/><label>Standard No.: </label>10.1007/0-306-47384-4_12  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Azepines--chemical synthesis<br/>Binding Sites<br/>Drug Design<br/>HIV Protease--chemistry<br/>HIV Protease Inhibitors--chemical synthesis<br/>Humans<br/>Molecular Conformation<br/>Urea--analogs & derivatives