Enhanced Potency of Nucleotide–Dendrimer Conjugates as Agonists of the P2Y(14) Receptor: Multivalent Effect in G Protein-Coupled Receptor Recognition

Ítems similars

• Polyamidoamine (PAMAM) Dendrimer Conjugates of “Clickable” Agonists of the A(3) Adenosine Receptor and Coactivation of the P2Y(14) Receptor by a Tethered Nucleotide
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• Synthesis and Potency of Novel Uracil Nucleotides and Derivatives as P2Y(2) and P2Y(6) Receptor Agonists
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• Molecular Recognition in the P2Y(14) Nucleotide Receptor: Probing the Structurally Permissive Terminal Sugar Moiety of Uridine-5′-diphosphoglucose
  per: Ko, Hyojin, et al.
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• Structure Activity Relationship of Uridine 5′-Diphosphoglucose (UDP-Glucose) Analogues as Agonists of the Human P2Y(14) Receptor
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