Fragment‐Based Drug Design Facilitated by Protein‐Templated Click Chemistry: Fragment Linking and Optimization of Inhibitors of the Aspartic Protease Endothiapepsin

Documenti analoghi

• Fragment Linking and Optimization of Inhibitors of the Aspartic Protease Endothiapepsin: Fragment‐Based Drug Design Facilitated by Dynamic Combinatorial Chemistry
  di: Mondal, Milon, et al.
  Pubblicazione: (2016)
• Design and Synthesis of Bioisosteres of Acylhydrazones as Stable Inhibitors of the Aspartic Protease Endothiapepsin
  di: Jumde, Varsha R., et al.
  Pubblicazione: (2018)
• Structure-Based Optimization of Inhibitors of the Aspartic Protease Endothiapepsin
  di: Hartman, Alwin M., et al.
  Pubblicazione: (2015)
• Applications of Click Chemistry in the Development of HIV Protease Inhibitors
  di: Mudgal, Mukesh M., et al.
  Pubblicazione: (2018)
• Poly(A)-ClickSeq: click-chemistry for next-generation 3΄-end sequencing without RNA enrichment or fragmentation
  di: Routh, Andrew, et al.
  Pubblicazione: (2017)