Synthesis and characterization of high-affinity 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene-labeled fluorescent ligands for human ?-adrenoceptors

Baker, Jillian G.; Adams, Luke A.; Salchow, Karolina; Mistry, Shailesh N.; Middleton, Richard J.; Hill, Stephen J.; Kellam, Barrie

Abstract

The growing practice of exploiting noninvasive fluorescence-based techniques to study G protein-coupled receptor pharmacology at the single cell and single molecule level demands the availability of high-quality fluorescent ligands. To this end, this study evaluated a new series of red-emitting ligands for the human ?-adrenoceptor family. Upon the basis of the orthosteric ligands propranolol, alprenolol, and pindolol, the synthesized linker-modified congeners were coupled to the commercially available fluorophore BODIPY 630/650-X. This yielded high-affinity ?-adrenoceptor fluorescent ligands for both the propranolol and alprenolol derivatives; however, the pindolol-based products displayed lower affinity. A fluorescent diethylene glycol linked propranolol derivative (18a) had the highest affinity (log KD of ?9.53 and ?8.46 as an antagonist of functional ?2- and ?1-mediated responses, respectively). Imaging studies with this compound further confirmed that it can be employed to selectively label the human ?2-adrenoceptor in single living cells, with receptor-associated binding prevented by preincubation with the nonfluorescent ?2-selective antagonist 3-(isopropylamino)-1-[(7-methyl-4-indanyl)oxy]butan-2-ol (ICI 118551)

Citation

Baker, J. G., Adams, L. A., Salchow, K., Mistry, S. N., Middleton, R. J., Hill, S. J., & Kellam, B. (2011). Synthesis and characterization of high-affinity 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene-labeled fluorescent ligands for human ?-adrenoceptors. Journal of Medicinal Chemistry, 54(19), 6874-6887. doi:10.1021/jm2008562

• Journal Article Type: Article
• Acceptance Date: Aug 29, 2011
• Online Publication Date: Aug 29, 2011
• Publication Date: Oct 13, 2011
• Deposit Date: Nov 23, 2018
• Publicly Available Date: Jan 31, 2019
• Journal: Journal of Medicinal Chemistry
• Print ISSN: 0022-2623
• Electronic ISSN: 1520-4804
• Publisher: American Chemical Society
• Peer Reviewed: Peer Reviewed
• Volume: 54
• Issue: 19
• Pages: 6874-6887
• DOI: https://doi.org/10.1021/jm2008562
• Public URL: https://nottingham-repository.worktribe.com/output/1304279
• Publisher URL: https://pubs.acs.org/doi/abs/10.1021/jm2008562