| Characteristics | |||||||
| Molecular Formula | C₂₂₁H₃₄₂N₄₆O₆₈ | ||||||
| CAS Number | 2381089-83-2 | ||||||
| Molar Mass | 4731.33 g/mo | ||||||
| Amino Acid Sequence | Tyr-Aib-Gln-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Ile-α-Me-Leu-Leu-Asp-Lys-C20-diacid-Ala-Gln-Aib-Ala-Phe-Ile-Glu-Trp-Leu-Lys-Asn-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Pro-Ser-NH₂ | ||||||
| Synonyms | LY3437943, Retatrutide, Triple Agonist Peptide | ||||||
| Solubilit | Water-soluble | ||||||
| rganoleptic Profile | White to off-white lyophilized powder | ||||||
| Composition | Lyophilized powder-requires reconstitution | ||||||
Product Introduction:
Retatrutide is a novel synthetic peptide that acts as a pioneering triple-hormone receptor agonist, garnering remarkable attention in the field of metabolic and obesity research. Structurally derived and optimized from the glucose-dependent insulinotropic polypeptide (GIP) backbone with specific modifications, it exhibits unique potency profile by potently activating three key receptors: Glucagon-like peptide-1 (GLP-1), Glucose-dependent insulinotropic polypeptide (GIP), and Glucagon receptors simultaneously, far exceeding the single-target scope of conventional GLP-1 receptor agonists . This distinctive triple-agonism mechanism triggers a comprehensive cascade of physiological responses, including robust suppression of appetite, significant acceleration of energy expenditure, synergistic regulation of glucose homeostasis, and effective reduction of hepatic fat content. Clinically, it has demonstrated exceptional efficacy in weight management, with substantial body weight reduction and marked improvements in metabolic indicators. Requires reconstitution before use.
- How does Retatrutide work?
Retatrutide exerts its effects through multiple interconnected receptor activation mechanisms:
Multi-Receptor Activation: Retatrutide is a triple agonist that binds to and activates GLP-1 (glucagon-like peptide-1), GIP (glucose-dependent insulinotropic polypeptide), and glucagon receptors, which are expressed in key tissues including pancreatic islets, the gastrointestinal tract, adipose tissue, liver, and the central nervous system. This co-activation initiates synergistic intracellular signaling cascades, primarily through cyclic AMP (cAMP) and protein kinase A (PKA) pathways.
Pancreatic Effects: In pancreatic β-cells, retatrutide enhances glucose-stimulated insulin secretion by elevating intracellular cAMP levels, while simultaneously suppressing glucagon release from α-cells, contributing to robust glycemic control.
Central Nervous System Effects: Retatrutide crosses the blood-brain barrier and acts on GLP-1, GIP, and glucagon receptors in the hypothalamus and brainstem. This central action regulates appetite, energy expenditure, and satiety signaling, driving reduced food intake.
- Research
Glucose Homeostasis: Retatrutide stimulates glucose-dependent insulin secretion from pancreatic β-cells while suppressing glucagon release, leading to significant improvements in glycemic control in individuals with type 2 diabetes mellitus (T2DM).
Appetite Regulation & Satiety: By co-activating GLP-1, GIP, and glucagon receptors in the hypothalamus and appetite-regulating brain regions, retatrutide reduces food intake, prolongs satiety, and lowers cravings, resulting in far greater weight loss efficacy than single GLP-1 agonists.
Body Weight Reduction: Through its synergistic effects on appetite suppression, increased energy expenditure, and enhanced fat metabolism, retatrutide has demonstrated unprecedented, clinically significant weight reduction in multiple clinical studies.
Cardiometabolic Benefits: Research indicates that retatrutide improves multiple cardiovascular risk factors, including lipid profiles (reduced triglycerides, LDL cholesterol), blood pressure, and hepatic steatosis, offering broad cardiometabolic protection.
Additional Metabolic Effects: Retatrutide has shown potential benefits in improving non-alcoholic steatohepatitis (NASH), reducing visceral fat, and enhancing overall metabolic health in preclinical and clinical research.
- Side Effects
The most common side effects associated with Retatrutide include:
Nausea
Vomiting
Diarrhea
Abdominal pain
Constipation
Headache
Fatigue
Gastrointestinal discomfort
- Summary
Retatrutide represents a groundbreaking advancement in multi-receptor agonist research, offering a potent, synergistic tool for investigating the complex interplay of GLP-1, GIP, and glucagon signaling in metabolic physiology. Its demonstrated efficacy in profound glycemic control, unprecedented weight management, and broad cardiometabolic benefits makes it a transformative subject for ongoing research in the treatment of T2DM, obesity, NASH, and related metabolic disorders. As investigations continue, retatrutide may unlock novel therapeutic strategies to address the global burden of metabolic and cardiovascular diseases.
- Resource
All products on this site are for research and development use only. Products are not for human consumption of any kind. The statements made on this website have not been evaluated by the US Food and Drug Administration. The statements and the products of this company are not intended to diagnose, treat, cure, or prevent any disease. Power Peptides is not a compounding pharmacy or chemical compounding facility as defined under 503A of the Federal Food, Drug, and Cosmetic Act. Power Peptides is not an outsourcing facility as defined under 503B of the Federal Food, Drug, and Cosmetic Act. All products are sold for research, laboratory, or analytical purposes only, and are not for human consumption. Power Peptides Products are intended strictly for research purposes only. These products are not approved by the U.S. Food and Drug Administration (FDA) for human consumption or medical use. Under no circumstances should these peptides be used for any purpose other than research. By purchasing or using our peptides, you acknowledge and agree that you will use them solely in accordance with applicable laws and regulations and that you accept full responsibility for their use. Statements made on this website have not been evaluated by the USA Food and Drug Administration.










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