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Drug Development Research|July 5, 2022
Acyl-Hydrazide Derivatives of a Xanthine Carboxylic Congener (XCC) as Selective Antagonists at Human A2B Adenosine ReceptorsYong-Chul Kim, Yishai Karton, Xiao-Duo Ji, et al.
Chemical Science|June 24, 2021
Ligand design by targeting a binding site waterPierre Matricon, R Rama Suresh, Zhan-Guo Gao, et al.
ACS Medicinal Chemistry Letters|August 23, 2011
Truncated (N)-Methanocarba Nucleosides as A(1) Adenosine Receptor Agonists and Partial Agonists: Overcoming Lack of a Recognition ElementDilip K Tosh, Khai Phan, Francesca Deflorian, et al.
Nucleic Acids Symposium Series (2004)|December 8, 2006
Development of potent and selective human A3 adenosine receptor agonistsLak Shin Jeong, Hyuk Woo Lee, Kenneth A Jacobson, et al.
Plos One|November 28, 2012
Limits of ligand selectivity from docking to models: in silico screening for A(1) adenosine receptor antagonistsPeter Kolb, Khai Phan, Zhan-Guo Gao, et al.
Drug Development Research|January 17, 2024
Species Differences in Ligand Affinity at Central A3-Adenosine ReceptorsXiao-Duo Ji, Dag von Lubitz, Mark E Olah, et al.
Cells|July 13, 2026
Perturbing O-GlcNAcase Modulates the Expression and Distribution of Galectin-3Mana Mohan Mukherjee, Asmita Pramanik, Marcella Kolodrubetz, et al.
Purinergic Signalling|July 5, 2008
Application of the functionalized congener approach to dendrimer-based signaling agents acting through A(2A) adenosine receptorsYoonkyung Kim, Athena M Klutz, Béatrice Hechler, et al.
Biochemical Pharmacology|April 15, 2004
Diisothiocyanate derivatives as potent, insurmountable antagonists of P2Y6 nucleotide receptorsLiaman K Mamedova, Bhalchandra V Joshi, Zhan-Guo Gao, et al.
Scientific Reports|July 25, 2018
Author Correction: Salvianolic acids from antithrombotic Traditional Chinese Medicine Danshen are antagonists of human P2Y1 and P2Y12 receptorsXuyang Liu, Zhan-Guo Gao, Yiran Wu, et al.
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