Design and Synthesis of HIV-1 Protease Inhibitors Incorporating Oxazolidinones as P2/P2′ Ligands in Pseudosymmetric Dipeptide Isosteres

Lignende værker

• Structure-Based Design, Synthesis and Structure-Activity Relationship Studies of HIV-1 Protease Inhibitors Incorporating Phenyloxazolidinones
  af: Ali, Akbar, et al.
  Udgivet: (2010)
• 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)
• Structural Analysis of Potent Hybrid HIV-1 Protease Inhibitors Containing Bis-Tetrahydrofuran in a Pseudo-Symmetric Dipeptide Isostere
  af: Rusere, Linah N., et al.
  Udgivet: (2020)
• Recent progress in the racemic and enantioselective synthesis of monofluoroalkene-based dipeptide isosteres
  af: Drouin, Myriam, et al.
  Udgivet: (2017)