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- W2800816519 abstract "Adenosine receptors are a family of GPCRs containing four subtypes (A 1 , A 2A , A 2B and A 3 receptors), all of which bind the ubiquitous nucleoside adenosine. These receptors play an important role in physiology and pathophysiology and therefore represent attractive drug targets for a range of conditions. The theoretical framework surrounding drug action at adenosine receptors now extends beyond the notion of prototypical agonism and antagonism to encompass more complex pharmacological concepts. New paradigms include allostery, in which ligands bind a topographically distinct receptor site from that of the endogenous agonist, homomeric or heteromeric interactions across receptor oligomers and biased agonism, that is, ligand‐dependent differential intracellular signalling. This review provides a concise overview of allostery, oligomerization and biased agonism at adenosine receptors and outlines how these paradigms may enhance future drug discovery endeavours focussed on the development of novel therapeutic agents acting at adenosine receptors. Linked Articles This article is part of a themed section on Molecular Pharmacology of GPCRs. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v175.21/issuetoc" @default.
- W2800816519 created "2018-05-17" @default.
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- W2800816519 date "2018-06-21" @default.
- W2800816519 modified "2023-10-04" @default.
- W2800816519 title "New paradigms in adenosine receptor pharmacology: allostery, oligomerization and biased agonism" @default.
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- W2800816519 doi "https://doi.org/10.1111/bph.14337" @default.
- W2800816519 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6177620" @default.
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