2-Substituted (N)-Methanocarba A3Adenosine Receptor Agonists: in Silico, in Vitro and in Vivo Characterization
ACS pharmacology & translational science(2024)
Abstract
2-Arylethynyl (N)-methanocarba adenosine 5 '-methylamides are selective A(3) adenosine receptor (AR) agonists containing a preestablished receptor-preferred pseudoribose conformation. Here, we compare analogues having bulky 2-substitution, either containing or lacking an ethynyl spacer between adenine and a cyclic group. 2-Aryl compounds 9-11, 13, 14, 19, 22, 23, 27, 29, 31, and 34, lacking a spacer, had human (h) A(3)AR K-i values of 2-30 nM, and others displayed lower affinity. Mouse (m) A(3)AR affinity varied, with 2-arylethynyl having a higher affinity than 2-aryl analogues (7, 8 > 3c, 3d > 3b). However, 2-aryl-4 '-truncated derivatives had greatly reduced hA(3)AR affinity, even containing affinity-enhancing N-6-dopamine-derived substituents. Molecular modeling, including molecular dynamics simulation, predicted stable poses in the canonical A(3)AR agonist binding site, but 2-aryl (ECL2 interactions) and 2-arylethynyl (TM2 interactions) substituents have different conformations and environments. In a hA(3)AR miniG alpha(i) recruitment assay, 31 (MRS8062) was (slightly) more potent compared to a beta-arrestin2 recruitment assay, both in engineered HEK293T cells, and its maximal efficacy (E-max) was much higher (165%) than reference agonist NECA's. Thus, in the 2-aryl series, A(3)AR affinity and selectivity were variable and generally reduced compared to the 2-arylethynyl series, with a greater dependence on the specific aryl group present. Selected compounds were studied in vivo in an ischemic model of peripheral artery disease (PAD). Rigidified 2-arylethynyl analogues 3a-3c were protective in this model of skeletal muscle ischemia-reperfusion injury/claudication, as previously shown only for moderately A(3)AR-selective ribosides or (N)-methanocarba derivatives. Thus, we have expanded the A(3)AR agonist SAR for (N)-methanocarba adenosines.
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Key words
adenosine receptor,G protein-coupled receptor,nucleosides,G protein,arrestin,structure-activityrelationship
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