Johns, Brian A <br/><br/>
1,3,4-Oxadiazole substituted naphthyridines as HIV-1 integrase inhibitors. Part 2: SAR of the C5 position.  [electronic resource] 

 -  Bioorganic & medicinal chemistry letters  Mar 2009 
 - 1807-10 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1464-3405 
<br/><br/><label>Standard No.: </label>10.1016/j.bmcl.2009.01.089  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Motifs<br/>Anti-HIV Agents--chemical synthesis<br/>Chelating Agents--pharmacology<br/>Chemistry, Pharmaceutical--methods<br/>Drug Design<br/>HIV Infections--drug therapy<br/>HIV Integrase Inhibitors--chemical synthesis<br/>Humans<br/>Metals--chemistry<br/>Models, Chemical<br/>Molecular Structure<br/>Naphthyridines--chemical synthesis<br/>Oxadiazoles--chemistry<br/>Structure-Activity Relationship<br/>Triazoles--chemistry