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Isoquinoline small molecule ligands are agonists and probe-dependent allosteric modulators of the glucagon subfamily of GPCRs.
- Source :
-
Biochemical pharmacology [Biochem Pharmacol] 2024 Nov; Vol. 229, pp. 116483. Date of Electronic Publication: 2024 Aug 13. - Publication Year :
- 2024
-
Abstract
- Class B1 G protein-coupled receptors (GPCRs) are peptide hormone receptors and well validated therapeutic targets, however development of non-peptide drugs targeting this class of receptors is challenging. Recently, a series of isoquinoline-based derivates were reported in the patent literature as allosteric ligands for the glucagon receptor subfamily, and two compounds, LSN3451217 and LSN3556672, were used to facilitate structural studies with the glucagon-like peptide-1 receptor (GLP-1R) and glucose dependent insulinotropic peptide receptor (GIPR) bound to orthosteric agonists. Here we pharmacologically characterized stereoisomers of LSN3451217 and LSN3556672, across the class B1 GPCR family. This revealed LSN3556672 isomers are agonists for the glucagon receptor (GCGR), GLP-1R, GIPR and the calcitonin receptor (CTR), albeit the degree of agonism varied at each receptor. In contrast, LSN3451217 isomers were more selective agonists at the GLP-1R, with lower potency at the GCGR and CTR and no activity at the GIPR. All compounds also modulated peptide-mediated cyclic adenosine monophosphate (cAMP) signaling at the GIPR, and to a lesser extent the GLP-1R, in a probe-dependent manner, with modest positive allosteric modulation observed for some peptides, and negligible effects observed with other peptides. In contrast neutral or weak negative/positive allosteric modulation was observed with peptides assessed at the GCGR and CTR. This study expands our knowledge on class B1 GPCR allosteric modulation and may have implications for future structural and drug discovery efforts targeting the class B1 GPCR subfamily.<br />Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: D.Wootten, P.M.S and A.C are co-founders of DACRA therapeutics. P.M.S and A.C are co-founders and scientific advisors, and D.W is a scientific advisory board member for Septerna Inc. R.E., H.N., D. Weichert are employees of Boehringer Ingelheim.<br /> (Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Humans
Ligands
Allosteric Regulation drug effects
Allosteric Regulation physiology
Glucagon-Like Peptide-1 Receptor agonists
Glucagon-Like Peptide-1 Receptor metabolism
HEK293 Cells
Animals
Cricetulus
Receptors, Gastrointestinal Hormone agonists
Receptors, Gastrointestinal Hormone metabolism
Receptors, Gastrointestinal Hormone chemistry
Small Molecule Libraries pharmacology
Small Molecule Libraries chemistry
CHO Cells
Receptors, Calcitonin agonists
Receptors, Calcitonin metabolism
Receptors, Calcitonin chemistry
Receptors, G-Protein-Coupled agonists
Receptors, G-Protein-Coupled metabolism
Receptors, G-Protein-Coupled chemistry
Glucagon metabolism
Glucagon agonists
Glucagon chemistry
Molecular Probes chemistry
Molecular Probes pharmacology
Isoquinolines pharmacology
Isoquinolines chemistry
Receptors, Glucagon agonists
Receptors, Glucagon metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1873-2968
- Volume :
- 229
- Database :
- MEDLINE
- Journal :
- Biochemical pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 39147328
- Full Text :
- https://doi.org/10.1016/j.bcp.2024.116483