Design and Synthesis of N(6)-Substituted-4′-thioadenosine-5′-uronamides As Potent and Selective Human A(3) Adenosine Receptor Agonists

Liknande verk

• Synthesis of 2-Chloro-N(6)-Substituted-4′-thioadenosine-5′-N,N-dialkyluronamides as Potent and Selective A(3) Adenosine Receptor Antagonists
  av: Choi, Won Jun, et al.
  Publicerad: (2008)
• Conversion of A(3) Adenosine Receptor Agonists into Selective Antagonists by Modification of the 5′-Ribofuran-uronamide Moiety
  av: Gao, Zhan-Guo, et al.
  Publicerad: (2005)
• Design and Synthesis of Truncated 4′-Thioadenosine Derivatives as Potent and Selective A(3) Adenosine Receptor Antagonists
  av: Hou, Xiyan, et al.
  Publicerad: (2008)
• Discovery of A New Human A(2A) Adenosine Receptor Agonist, Truncated 2-Hexynyl-4′-thioadenosine
  av: Hou, Xiyan, et al.
  Publicerad: (2010)
• Structure-Activity Relationships of Truncated D- and L-4′-Thioadenosine Derivatives as Species-Independent A(3) Adenosine Receptor Antagonists(1)
  av: Jeong, Lak Shin, et al.
  Publicerad: (2008)