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Journal of Medicinal Chemistry|August 26, 2021
Subtle Chemical Changes Cross the Boundary between Agonist and Antagonist: New A3 Adenosine Receptor Homology Models and Structural Network Analysis Can Predict This BoundaryYoonji Lee, Xiyan Hou, Jin Hee Lee, et al.Bioorganic & Medicinal Chemistry|April 21, 2009
Structure-activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonistsShantanu Pal, Won Jun Choi, Seung Ah Choe, et al.Journal of Medicinal Chemistry|September 25, 2008
Structure-activity relationships of truncated D- and l-4'-thioadenosine derivatives as species-independent A3 adenosine receptor antagonistsLak Shin Jeong, Shantanu Pal, Seung Ah Choe, et al.Journal of Medicinal Chemistry|August 17, 2022
GPCR Agonist-to-Antagonist Conversion: Enabling the Design of Nucleoside Functional Switches for the A2A Adenosine ReceptorAnna Shiriaeva, Daejin Park, Gyudong Kim, et al.Journal of Medicinal Chemistry|January 25, 2014
Synthesis and anti-renal fibrosis activity of conformationally locked truncated 2-hexynyl-N(6)-substituted-(N)-methanocarba-nucleosides as A3 adenosine receptor antagonists and partial agonistsAkshata Nayak, Girish Chandra, Inah Hwang, et al.Journal of Medicinal Chemistry|December 7, 2011
Structure-activity relationships of truncated C2- or C8-substituted adenosine derivatives as dual acting A₂A and A₃ adenosine receptor ligandsXiyan Hou, Mahesh S Majik, Kyunglim Kim, et al.Journal of Medicinal Chemistry|August 21, 2023
Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A2A/A3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic ActivityGibae Kim, Xiyan Hou, Woong Sub Byun, et al.Journal of Medicinal Chemistry|June 7, 2024
Structural Modification and Biological Evaluation of 2,8-Disubstituted Adenine and Its Nucleosides as A2A Adenosine Receptor Antagonists: Exploring the Roles of Ribose at Adenosine ReceptorsGibae Kim, Dnyandev B Jarhad, Grim Lee, et al.Pageof 3