Rigidified A(3) Adenosine Receptor Agonists: 1-Deazaadenine Modification Maintains High in Vivo Efficacy

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• Structure-Based Design, Synthesis by Click Chemistry and in Vivo Activity of Highly Selective A(3) Adenosine Receptor Agonists
  door: Tosh, Dilip K., et al.
  Gepubliceerd in: (2015)
• In Vivo Phenotypic Screening for Treating Chronic Neuropathic Pain: Modification of C2-Arylethynyl Group of Conformationally Constrained A(3) Adenosine Receptor Agonists
  door: Tosh, Dilip K., et al.
  Gepubliceerd in: (2014)
• Purine (N)-Methanocarba Nucleoside Derivatives Lacking an Exocyclic Amine as Selective A(3) Adenosine Receptor Agonists
  door: Tosh, Dilip K., et al.
  Gepubliceerd in: (2016)
• Scaffold Repurposing of Nucleosides (Adenosine Receptor Agonists): Enhanced Activity at the Human Dopamine and Norepinephrine Sodium Symporters
  door: Tosh, Dilip K., et al.
  Gepubliceerd in: (2017)
• Structural Probing of Off-Target G Protein-Coupled Receptor Activities within a Series of Adenosine/Adenine Congeners
  door: Paoletta, Silvia, et al.
  Gepubliceerd in: (2014)