Pegapamodutide, a cutting-edge biomedical marvel, emerges as a beacon of hope in the quest to mitigate the multifaceted manifestations of type 2 diabetes. Through intricate interactions with the esteemed GLP-1 receptors, this transcendent pharmaceutical masterpiece exerts its influence, stimulating insulin secretion contingent upon glucose levels and meticulously overseeing the delicate balance of blood glucose.
CAT No: R2066
CAS No:1492924-65-8
Synonyms/Alias:Pegapamodutide;Pegapamodutide [USAN];UNII-WG4ID2U7FT;WG4ID2U7FT;LY2944876;Pegapamodutide (USAN);pegapamodutida;pegapamodutidum;CAS Registry Number;PEGAPAMODUTIDE [INN];PEGAPAMODUTIDE [WHO-DD];LY-2944876;Q27292621;1492924-65-8;
Chemical Name:(2R)-2-amino-3-[1-[3-[3-(2-methoxyethoxy)propylamino]-3-oxopropyl]-2,5-dioxopyrrolidin-3-yl]sulfanylpropanoic acid
Pegapamodutide is a synthetic peptide-based compound engineered for advanced biochemical and pharmacological research applications. As a long-acting glucagon-like peptide-1 (GLP-1) receptor agonist conjugated with polyethylene glycol (PEG), it exhibits enhanced stability and prolonged activity compared to native peptide counterparts. Its structural design and functional properties make it a valuable tool for investigating peptide-receptor interactions, metabolic regulation, and the development of next-generation peptide therapeutics. The compound's unique PEGylation confers increased resistance to proteolytic degradation, enabling extended experimental timelines and improved reproducibility in laboratory settings.
Peptide receptor characterization: In receptor biology research, Pegapamodutide serves as a robust probe for studying GLP-1 receptor activation, signal transduction pathways, and ligand-binding dynamics. By providing a stable and selective agonist, it enables detailed analysis of downstream signaling events, receptor desensitization, and internalization processes. Researchers utilize this compound to dissect the molecular mechanisms that govern peptide hormone action and to map receptor-ligand interactions with high fidelity, facilitating the discovery of novel modulators or antagonists.
Metabolic pathway investigation: The compound is widely employed in studies focused on metabolic regulation and energy homeostasis. Its ability to mimic endogenous GLP-1 activity allows researchers to model the biochemical effects of incretin signaling on glucose metabolism, insulin secretion, and lipid processing. Such investigations are instrumental in elucidating the pathways underlying metabolic disorders and in identifying new targets for metabolic intervention at the preclinical research stage.
Peptide stability and pharmacokinetics: Pegapamodutide's PEGylated structure provides a model system for evaluating the impact of chemical modifications on peptide pharmacokinetics and stability. Scientists leverage its prolonged half-life and resistance to enzymatic degradation to assess how structural alterations can optimize peptide bioavailability and tissue distribution. These insights are essential for the rational design of peptide-based agents with improved in vivo performance and for developing predictive models of peptide behavior in biological systems.
Peptide synthesis and formulation research: The compound is also utilized as a reference standard for optimizing peptide synthesis protocols and formulation strategies. Its defined structure and PEGylation profile allow formulation scientists to test new delivery systems, study the impact of excipients on peptide integrity, and refine purification processes. Such work is critical for enhancing the manufacturability and scalability of complex peptide drugs and for ensuring batch-to-batch consistency in research and development environments.
Analytical method development: In analytical biochemistry, Pegapamodutide is used to validate and calibrate methods for peptide quantification, stability assessment, and bioanalytical detection. Its unique physicochemical properties make it an ideal candidate for developing robust LC-MS/MS assays, immunoassays, and chromatographic techniques tailored to long-acting peptide conjugates. Accurate analytical characterization of such compounds supports quality control, process optimization, and the advancement of peptide research technologies.
1. Store-operated Ca2+ entry sustains the fertilization Ca2+ signal in pig eggs
3. High fat diet and GLP-1 drugs induce pancreatic injury in mice
5. C-Peptide replacement therapy and sensory nerve function in type 1 diabetic neuropathy
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