Synthesis of 2-Chloro-N(6)-Substituted-4′-thioadenosine-5′-N,N-dialkyluronamides as Potent and Selective A(3) Adenosine Receptor Antagonists

Lignende værker

• Design and Synthesis of Truncated 4′-Thioadenosine Derivatives as Potent and Selective A(3) Adenosine Receptor Antagonists
  af: Hou, Xiyan, et al.
  Udgivet: (2008)
• Design and Synthesis of N(6)-Substituted-4′-thioadenosine-5′-uronamides As Potent and Selective Human A(3) Adenosine Receptor Agonists
  af: Choi, Won Jun, et al.
  Udgivet: (2009)
• Structure-Activity Relationships of Truncated D- and L-4′-Thioadenosine Derivatives as Species-Independent A(3) Adenosine Receptor Antagonists(1)
  af: Jeong, Lak Shin, et al.
  Udgivet: (2008)
• Structure-Activity Relationships of Truncated Adenosine Derivatives as Highly Potent and Selective Human A(3) Adenosine Receptor Antagonists
  af: Pal, Shantanu, et al.
  Udgivet: (2009)
• Design, Synthesis, and Binding Affinity of Homologated 4′-Thioadenosine Derivatives at the human A(3) Adenosine receptor
  af: Lee, Hyuk Woo, et al.
  Udgivet: (2010)