The best of both worlds? Bitopic orthosteric/allosteric ligands of g protein-coupled receptors

Valant, Celine; Lane, Jonathan R; Sexton, Patrick M; Christopoulos, Arthur

Abstract

It is now acknowledged that G protein-coupled receptors, the largest class of drug targets, adopt multiple active states that can be preferentially stabilized by orthosteric ligands or allosteric modulators, thus giving rise to the phenomenon of pathway-biased signaling. In the past few years, researchers have begun to explore the potential of linking orthosteric and allosteric pharmacophores to yield bitopic hybrid ligands. This approach is an extension of the more traditional bivalent ligand concept and shares some of the same challenges, including the choice and role of the linker between the two pharmacophores and the validation of mechanism of action. Nonetheless, the promise of bitopic ligands is the generation of novel chemical tools that have improved affinity and/or selectivity profiles. Previously identified functionally selective compounds (and medicines) also may act via a bitopic mechanism, suggesting that the phenomenon is more widespread than currently appreciated.

Citation

Valant, C., Lane, J. R., Sexton, P. M., & Christopoulos, A. (2012). The best of both worlds? Bitopic orthosteric/allosteric ligands of g protein-coupled receptors. Annual Review of Pharmacology and Toxicology, 52, 153-178. https://doi.org/10.1146/annurev-pharmtox-010611-134514

• Journal Article Type: Review
• Online Publication Date: Sep 9, 2011
• Publication Date: 2012-02
• Deposit Date: Apr 22, 2020
• Print ISSN: 0362-1642
• Electronic ISSN: 1545-4304
• Publisher: Annual Reviews
• Peer Reviewed: Peer Reviewed
• Volume: 52
• Pages: 153-178
• DOI: https://doi.org/10.1146/annurev-pharmtox-010611-134514
• Public URL: https://nottingham-repository.worktribe.com/output/1339708
• Publisher URL: https://www.annualreviews.org/doi/10.1146/annurev-pharmtox-010611-134514
• Related Public URLs: http://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=21910627&retmode=ref&cmd=prlinks