Potent agonist action of 2-thioether derivatives of adenine nucleotides at adenylyl cyclase-linked P2Y-purinoceptors.

Ítems similars

• Differential effects of P2-purinoceptor antagonists on phospholipase C- and adenylyl cyclase-coupled P2Y-purinoceptors.
  per: Boyer, J L, et al.
  Publicat: (1994)
• Identification of potent P2Y-purinoceptor agonists that are derivatives of adenosine 5'-monophosphate.
  per: Boyer, J. L., et al.
  Publicat: (1996)
• Identification of Potent, Selective P(2Y)-Purinoceptor Agonists: Structure–Activity Relationships for 2-Thioether Derivatives of Adenosine 5′-Triphosphate
  per: Fischer, Bilha, et al.
  Publicat: (1993)
• Quantification of G(i)-Mediated Inhibition of Adenylyl Cyclase Activity Reveals That UDP Is a Potent Agonist of the Human P2Y(14) Receptor
  per: Carter, Rhonda L., et al.
  Publicat: (2009)
• Enzymatic synthesis of UTP gamma S, a potent hydrolysis resistant agonist of P2U-purinoceptors.
  per: Lazarowski, E. R., et al.
  Publicat: (1996)