PMID
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Article Title
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Molecular modeling of the human P2Y14 receptor: A template for structure-based design of selective agonist ligands.

National Institute of Diabetes and Digestive and Kidney Diseases
Discovery of 2-(phenoxypyridine)-3-phenylureas as small molecule P2Y1 antagonists.

Bristol-Myers Squibb Research and Development
Human P2Y(14) receptor agonists: truncation of the hexose moiety of uridine-5'-diphosphoglucose and its replacement with alkyl and aryl groups.

National Institute of Diabetes and Digestive and Kidney Diseases
Molecular dynamics simulation of the P2Y14 receptor. Ligand docking and identification of a putative binding site of the distal hexose moiety.

National Institute of Diabetes and Digestive and Kidney Diseases
The identification of 4,7-disubstituted naphthoic acid derivatives as UDP-competitive antagonists of P2Y14.

Merck Frosst Centre For Therapeutic Research
Synthesis and SAR of pyrimidine-based, non-nucleotide P2Y14 receptor antagonists.

Merck Frosst Center For Therapeutic Research
Pyrimidine ribonucleotides with enhanced selectivity as P2Y(6) receptor agonists: novel 4-alkyloxyimino, (S)-methanocarba, and 5'-triphosphate gamma-ester modifications.

National Institute of Diabetes and Digestive and Kidney Diseases
Molecular recognition in the P2Y(14) receptor: Probing the structurally permissive terminal sugar moiety of uridine-5'-diphosphoglucose.

National Institute of Diabetes and Digestive and Kidney Diseases
Discovery of N-Substituted Acetamide Derivatives as Promising P2Y14R Antagonists Using Molecular Hybridization Based on Crystallographic Overlay.

Children's Hospital Affiliated to Zhengzhou University
Structure-activity relationship of uridine 5'-diphosphoglucose analogues as agonists of the human P2Y14 receptor.

National Institute of Diabetes and Digestive and Kidney Diseases
Alicyclic Ring Size Variation of 4-Phenyl-2-naphthoic Acid Derivatives as P2Y

National Institute of Diabetes and Digestive and Kidney Diseases
Drug-like Antagonists of P2Y Receptors-From Lead Identification to Drug Development.

University of Nottingham
Discovery of a Series of 5-Amide-1

China Pharmaceutical University
Discovery and computational studies of 2-phenyl-benzoxazole acetamide derivatives as promising P2Y

Soochow University
Bridged Piperidine Analogues of a High Affinity Naphthalene-Based P2Y

National Institute of Diabetes and Digestive and Kidney Diseases
Structure-activity relationships of pyrimidine nucleotides containing a 5'-α,β-methylene diphosphonate at the P2Y

National Institute of Diabetes and Digestive and Kidney Diseases
Design, synthesis and evaluation of 3-amide-5-aryl benzoic acid derivatives as novel P2Y

China Pharmaceutical University
Structure-Activity Relationship of Heterocyclic P2Y

National Institute of Diabetes and Digestive and Kidney Diseases
Exploration of Alternative Scaffolds for P2Y

National Institute of Diabetes and Digestive and Kidney Diseases
P2Y

Saint Louis University School of Medicine
Structure-Based Design of 3-(4-Aryl-1H-1,2,3-triazol-1-yl)-Biphenyl Derivatives as P2Y14 Receptor Antagonists.

National Institute of Diabetes and Digestive and Kidney Diseases
Structure-Activity Relationship of Purine and Pyrimidine Nucleotides as Ecto-5'-Nucleotidase (CD73) Inhibitors.

National Institute of Diabetes and Digestive and Kidney Diseases
Design, synthesis and anti-inflammatory evaluation of 3-amide benzoic acid derivatives as novel P2Y

China Pharmaceutical University
Recent progress on the discovery of P2Y

China Pharmaceutical University
Structure-Guided Modification of Heterocyclic Antagonists of the P2Y

National Institute of Diabetes and Digestive and Kidney Diseases
Benzodioxane inhibitors of leukotriene production for combination therapy

Boehringer Ingelheim International