5-OMe-UDP is a Potent and Selective P2Y6-Receptor Agonist
Author:
Affiliation:
1. Department of Chemistry, Gonda-Goldschmied Medical Research Center, Bar-Ilan University, Ramat-Gan 52900, Israel
2. Institute for Neurobiochemistry, Faculty of Medicine, Otto von Guericke University, Leipziger Str. 44 D-39120 Magdeburg, Germany
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm901450d
Reference47 articles.
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2. Pharmacology of INS37217 [P1-(Uridine 5′)-P4- (2′-deoxycytidine 5′)tetraphosphate, Tetrasodium Salt], a Next-Generation P2Y2 Receptor Agonist for the Treatment of Cystic Fibrosis
3. Nucleotides and dinucleotides in ocular physiology: New possibilities of nucleotides as therapeutic agents in the eye
4. ATP gradients inhibit the migratory capacity of specific human dendritic cell types: implications for P2Y11 receptor signaling
5. Growth inhibition of lung cancer cells by adenosine 5?-triphosphate
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