Structure-Based Design, Synthesis and Structure-Activity Relationship Studies of HIV-1 Protease Inhibitors Incorporating Phenyloxazolidinones

Lignende værker

• Design and Synthesis of HIV-1 Protease Inhibitors Incorporating Oxazolidinones as P2/P2′ Ligands in Pseudosymmetric Dipeptide Isosteres
  af: Kiran Kumar Reddy, G. S., et al.
  Udgivet: (2007)
• Design, Synthesis, Biological and Structural Evaluations of Novel HIV-1 Protease Inhibitors to Combat Drug Resistance
  af: Parai, Maloy Kumar, et al.
  Udgivet: (2012)
• Substrate Envelope Designed Potent HIV-1 Protease Inhibitors to Avoid Drug Resistance
  af: Nalam, Madhavi N.L., et al.
  Udgivet: (2013)
• HIV-1 Protease Inhibitors from Inverse Design in the Substrate Envelope Exhibit Subnanomolar Binding to Drug-Resistant Variants
  af: Altman, Michael D., et al.
  Udgivet: (2008)
• Additivity in the Analysis and Design of HIV Protease Inhibitors
  af: Jorissen, Robert N., et al.
  Udgivet: (2009)