Structure-Based Design, Synthesis by Click Chemistry and in Vivo Activity of Highly Selective A(3) Adenosine Receptor Agonists

Lignende værker

• Rigidified A(3) Adenosine Receptor Agonists: 1-Deazaadenine Modification Maintains High in Vivo Efficacy
  af: Tosh, Dilip K., et al.
  Udgivet: (2015)
• In Vivo Phenotypic Screening for Treating Chronic Neuropathic Pain: Modification of C2-Arylethynyl Group of Conformationally Constrained A(3) Adenosine Receptor Agonists
  af: Tosh, Dilip K., et al.
  Udgivet: (2014)
• Purine (N)-Methanocarba Nucleoside Derivatives Lacking an Exocyclic Amine as Selective A(3) Adenosine Receptor Agonists
  af: Tosh, Dilip K., et al.
  Udgivet: (2016)
• Scaffold Repurposing of Nucleosides (Adenosine Receptor Agonists): Enhanced Activity at the Human Dopamine and Norepinephrine Sodium Symporters
  af: Tosh, Dilip K., et al.
  Udgivet: (2017)
• Design and in vivo activity of A(3) adenosine receptor agonist prodrugs
  af: Suresh, R. Rama, et al.
  Udgivet: (2020)