Oximinoarylsulfonamides as potent HIV protease inhibitors. [electronic resource]
- Bioorganic & medicinal chemistry letters May 2005
- 2275-8 p. digital
Publication Type: Journal Article
0960-894X
10.1016/j.bmcl.2005.03.008 doi
Binding Sites Carbamates Drug Design Furans HIV Protease--chemistry HIV Protease Inhibitors--chemical synthesis Kinetics Lopinavir Models, Molecular Molecular Conformation Pyrimidinones--chemistry Ritonavir--chemistry Sulfonamides--chemical synthesis