Jungheim, L N <br/><br/>
Potent human immunodeficiency virus type 1 protease inhibitors that utilize noncoded D-amino acids as P2/P3 ligands.  [electronic resource] 

 -  Journal of medicinal chemistry  Jan 1996 
 - 96-108 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0022-2623 
<br/><br/><label>Standard No.: </label>10.1021/jm950576c  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acids--metabolism<br/>Animals<br/>Antiviral Agents--chemical synthesis<br/>Biological Availability<br/>Cysteine--analogs & derivatives<br/>Drug Design<br/>HIV Protease--metabolism<br/>HIV Protease Inhibitors--chemical synthesis<br/>HIV-1--drug effects<br/>Humans<br/>Ligands<br/>Magnetic Resonance Spectroscopy<br/>Male<br/>Mass Spectrometry<br/>Molecular Structure<br/>Protein Binding<br/>Rats<br/>Rats, Sprague-Dawley<br/>Structure-Activity Relationship<br/>Sulfones--chemical synthesis