Mechanism-Based Inhibitors of Serine Proteases with High Selectivity Through Optimization of S’ Subsite Binding

समान संसाधन

• Design, Synthesis and In Vitro Evaluation of Potential West Nile Virus Protease Inhibitors Based on the 1-Oxo-1, 2, 3, 4-tetrahydroisoquinoline and 1-Oxo-1, 2-dihydroisoquinoline Scaffolds
  द्वारा: Dou, Dengfeng, और अन्य
  प्रकाशित: (2010)
• Dual Function Inhibitors of Relevance to Chronic Obstructive Pulmonary Disease
  द्वारा: Dou, Dengfeng, और अन्य
  प्रकाशित: (2010)
• Utilization of the 1, 2, 3, 5-Thiatriazolidin-3-one 1, 1-Dioxide Scaffold in the Design of Potential Inhibitors of Human Neutrophil Proteinase 3
  द्वारा: Dou, Dengfeng, और अन्य
  प्रकाशित: (2009)
• Inhibitors of human neutrophil elastase based on a highly functionalized N-amino-4-imidazolidinone scaffold
  द्वारा: He, Guijia, और अन्य
  प्रकाशित: (2010)
• The conformational change in rhomboid protease GlpG induced by inhibitor binding to its S’-subsites
  द्वारा: Xue, Yi, और अन्य
  प्रकाशित: (2012)