4-Alkyloxyimino Derivatives of Uridine-5′-triphosphate: Distal Modification of Potent Agonists as a Strategy for Molecular Probes of P2Y(2), P2Y(4), and P2Y(6) Receptors

समान संसाधन

• Pyrimidine Ribonucleotides with Enhanced Selectivity as P2Y(6) Receptor Agonists: Novel 4-Alkyloxyimino, (S)-Methanocarba, and 5′-Triphosphate γ-Ester Modifications
  द्वारा: Maruoka, Hiroshi, और अन्य
  प्रकाशित: (2010)
• 4-Alkyloxyimino-cytosine nucleotides: tethering approaches to molecular probes for the P2Y(6) receptor()
  द्वारा: Jayasekara, P. Suresh, और अन्य
  प्रकाशित: (2013)
• Pyrimidine Nucleotides with 4-Alkyloxyimino and Terminal Tetraphosphate δ-Ester Modifications as Selective Agonists of the P2Y(4) Receptor
  द्वारा: Maruoka, Hiroshi, और अन्य
  प्रकाशित: (2011)
• Structure activity and molecular modeling analyses of ribose- and base-modified uridine 5′-triphosphate analogues at the human P2Y(2) and P2Y(4) receptors
  द्वारा: Jacobson, Kenneth A., और अन्य
  प्रकाशित: (2005)
• Synthesis and P2Y(2) Receptor Agonist Activities of Uridine 5’-Phosphonate Analogues
  द्वारा: Van Poecke, Sara, और अन्य
  प्रकाशित: (2012)