Synthesis and activity of N-acyl azacyclic urea HIV-1 protease inhibitors with high potency against multiple drug resistant viral strains. [electronic resource]
- Bioorganic & medicinal chemistry letters Dec 2005
- 5499-503 p. digital
Publication Type: Journal Article
0960-894X
10.1016/j.bmcl.2005.08.093 doi
Aza Compounds--chemical synthesis Drug Design Drug Resistance, Multiple HIV Protease Inhibitors--chemical synthesis HIV-1--drug effects Ligands Microbial Sensitivity Tests Models, Molecular Ritonavir--chemical synthesis Structure-Activity Relationship Urea--analogs & derivatives