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We discuss the use of glucagon-like peptide-1 (GLP-1) analogues as monotherapy and unimolecular dual or triple agonists that exploit the GLP-1 receptor and/or the gastric inhibitory peptide (GIP) receptor and/or the glucagon receptor

These compounds are commonly referenced in GLP-1 receptor and metabolic signaling research, where peptides are studied for their interaction with biological pathways related to energy regulation, endocrine signaling, and peptide receptor activity

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