Discovery of A New Human A(2A) Adenosine Receptor Agonist, Truncated 2-Hexynyl-4′-thioadenosine

Ítems similars

• Design and Synthesis of Truncated 4′-Thioadenosine Derivatives as Potent and Selective A(3) Adenosine Receptor Antagonists
  per: Hou, Xiyan, et al.
  Publicat: (2008)
• Synthesis and Anti-Renal Fibrosis Activity of Conformationally Locked Truncated 2-Hexynyl-N(6)-Substituted-(N)-Methanocarba-nucleosides as A(3) Adenosine Receptor Antagonists and Partial Agonists
  per: Nayak, Akshata, et al.
  Publicat: (2014)
• Design, Synthesis, and Binding Affinity of Homologated 4′-Thioadenosine Derivatives at the human A(3) Adenosine receptor
  per: Lee, Hyuk Woo, et al.
  Publicat: (2010)
• Synthesis of 2-Chloro-N(6)-Substituted-4′-thioadenosine-5′-N,N-dialkyluronamides as Potent and Selective A(3) Adenosine Receptor Antagonists
  per: Choi, Won Jun, et al.
  Publicat: (2008)
• Structure-Activity Relationships of Truncated C2- or C8-Substituted Adenosine Derivatives as Dual Acting A(2A) and A(3) Adenosine Receptor Ligands
  per: Hou, Xiyan, et al.
  Publicat: (2011)