RetatrutideΒ is a GGG tri-agonist that targets GLP-1 and GIP receptors, akin to standard GLP-1 agonists, but also uniquely activates the glucagon receptor. This extra receptor interaction enhances glucagon production, leading to the breakdown of stored fats and glycogen, thereby increasing basal metabolism for more consistent fat loss. Its actions on GLP-1 and GIP receptors promote delayed gastric emptying and appetite control, offering a comprehensive approach to obesity research distinct from older GLP-1 agonists. Further research is required.
$230.00
Retatrutide (LY3437943) is a synthetic peptide designed as a triple agonist for the GLP-1, GIP, and glucagon receptors. This unique mechanism positions Retatrutide as a valuable compound in metabolic research, particularly in studies related to obesity, type 2 diabetes, and non-alcoholic fatty liver disease (NAFLD).
β οΈ For Research Use Only β Not for human consumption or therapeutic applications.
Retatrutide simultaneously activates three key receptors involved in metabolic regulation:
This triagonist approach offers a synergistic effect, potentially leading to superior outcomes in metabolic research compared to single or dual agonist compounds.
Retatrutide has been generally well-tolerated in preclinical and early human studies. Mild GI symptoms such as nausea and diarrhea have been observed, typically decreasing over time.
Note: Research use only. Not approved for human or veterinary applications.
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