Selective Allosteric Antagonists for the G Protein-Coupled Receptor GPRC6A Based on the 2-Phenylindole Privileged Structure Scaffold

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Henrik Johansson, Michael Worch Boesgaard, Lenea Nørskov-Lauritsen, Inna Larsen, Sebastiaan Kuhne, David E Gloriam, Hans Bräuner-Osborne, Daniel Sejer Pedersen

G protein-coupled receptors (GPCRs) represent a biological target class of fundamental importance in drug therapy. The GPRC6A receptor is a newly deorphanized class C GPCR that we recently reported for the first allosteric antagonists based on the 2-arylindole privileged structure scaffold (e.g., 1-3). Herein, we present the first structure-activity relationship study for the 2-arylindole antagonist 3, comprising the design, synthesis, and pharmacological evaluation of a focused library of 3-substituted 2-arylindoles. In a FRET-based inositol monophosphate (IP1) assay we identified compounds 7, 13e, and 34b as antagonists at the GPRC6A receptor in the low micromolar range and show that 7 and 34b display >9-fold selectivity for the GPRC6A receptor over related GPCRs, making 7 and 34b the most potent and selective antagonists for the GPRC6A receptor reported to date.

Original languageEnglish
JournalJournal of Medicinal Chemistry
Volume58
Issue number22
Pages (from-to)8938-51
Number of pages14
ISSN0022-2623
DOIs
Publication statusPublished - 25 Nov 2015

ID: 150328186