Design and Synthesis of Truncated 4′-Thioadenosine Derivatives as Potent and Selective A(3) Adenosine Receptor Antagonists

Gelijkaardige items

• Synthesis of 2-Chloro-N(6)-Substituted-4′-thioadenosine-5′-N,N-dialkyluronamides as Potent and Selective A(3) Adenosine Receptor Antagonists
  door: Choi, Won Jun, et al.
  Gepubliceerd in: (2008)
• Structure-Activity Relationships of Truncated Adenosine Derivatives as Highly Potent and Selective Human A(3) Adenosine Receptor Antagonists
  door: Pal, Shantanu, et al.
  Gepubliceerd in: (2009)
• Structure-Activity Relationships of Truncated D- and L-4′-Thioadenosine Derivatives as Species-Independent A(3) Adenosine Receptor Antagonists(1)
  door: Jeong, Lak Shin, et al.
  Gepubliceerd in: (2008)
• Discovery of A New Human A(2A) Adenosine Receptor Agonist, Truncated 2-Hexynyl-4′-thioadenosine
  door: Hou, Xiyan, et al.
  Gepubliceerd in: (2010)
• Design and Synthesis of N(6)-Substituted-4′-thioadenosine-5′-uronamides As Potent and Selective Human A(3) Adenosine Receptor Agonists
  door: Choi, Won Jun, et al.
  Gepubliceerd in: (2009)