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9 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Development of potent and selective inhibitors of ecto-5'-nucleotidase based on an anthraquinone scaffold.EBI
University of Bonn
5-OMe-UDP is a potent and selective P2Y(6)-receptor agonist.EBI
Bar-Ilan University
Identification of hydrolytically stable and selective P2Y(1) receptor agonists.EBI
Bar-Ilan University
Selective nucleoside triphosphate diphosphohydrolase-2 (NTPDase2) inhibitors: nucleotide mimetics derived from uridine-5'-carboxamide.EBI
University of Bonn
Combinatorial synthesis of anilinoanthraquinone derivatives and evaluation as non-nucleotide-derived P2Y2 receptor antagonists.EBI
University of Bonn
Synthesis and structure-activity relationships of uracil nucleotide derivatives and analogues as agonists at human P2Y2, P2Y4, and P2Y6 receptors.EBI
University of Bonn
Boranophosphate isoster controls P2Y-receptor subtype selectivity and metabolic stability of dinucleoside polyphosphate analogues.EBI
Bar-Ilan University
Structure activity relationship of 3-nitro-2-(trifluoromethyl)-2H-chromene derivatives as P2YEBI
National Institute of Diabetes and Digestive and Kidney Diseases
Design, synthesis and biological evaluation of suramin-derived dual antagonists of the proinflammatory G protein-coupled receptors P2YEBI
University of Bonn