Mak, C C <br/><br/>
Design, synthesis, and biological evaluation of HIV/FIV protease inhibitors incorporating a conformationally constrained macrocycle with a small P3' residue.  [electronic resource] 

 -  Bioorganic & medicinal chemistry letters  Jan 2001 
 - 219-22 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0960-894X 
<br/><br/><label>Standard No.: </label>10.1016/s0960-894x(00)00641-7  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Motifs<br/>Aminocaproates--chemistry<br/>Antiviral Agents--chemical synthesis<br/>Aspartic Acid Endopeptidases--antagonists & inhibitors<br/>Combinatorial Chemistry Techniques<br/>Drug Design<br/>Drug Resistance<br/>HIV Protease Inhibitors--chemical synthesis<br/>Immunodeficiency Virus, Feline--enzymology<br/>Inhibitory Concentration 50<br/>Molecular Conformation<br/>Molecular Mimicry<br/>Peptides, Cyclic--chemical synthesis<br/>Protease Inhibitors--chemical synthesis<br/>Structure-Activity Relationship