Synthesis and Biological Evaluation of 5'-Deoxy-adenosine Derivatives as A₃ Adenosine Receptor Ligands.

ABSTRACT: The A₃ Adenosine Receptor (A₃AR) is an important therapeutic target due to its role in inflammation and immune response regulation. Herein, we synthesized and evaluated 5'-deoxy-adenosine derivatives with oxygen at the 4'-position, comparing them to previously studied 4'-thionucleosides. Compound 1h exhibited the highest binding affinity (K _i = 5.9 ± 1.1 nM), consistent with the trend observed in the 4'-thionucleosides. Notably, the 5'-deoxy-adenosine derivatives demonstrated enhanced agonistic activity. Docking studies with compound 1h revealed a shift in binding mode when oxygen replaced sulfur at the 4'-position. The compounds retained strong interactions with critical residues, such as Thr94, even without a hydrogen bond donor at th

SUBMITTER: Kim M 

PROVIDER: S-EPMC11726369 | biostudies-literature | 2025 Jan

REPOSITORIES: biostudies-literature