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Retatrutide is an investigational triple hormone receptor agonist that targets the GLP-1 (glucagon-like peptide-1), GIP (glucose-dependent insulinotropic polypeptide), and glucagon receptors. Developed for the treatment of obesity and type 2 diabetes, Retatrutide represents a next-generation incretin-based therapy aimed at maximizing metabolic benefits such as weight loss, improved glycemic control, and lipid regulation.
Sequence:YA1QGTFTSDYSIL2LDKK4AQA1AFIEYLLEGGPSSGAPPPS3
Molecular Formula:C221H342N46O68
Molecular Weight: 4731.33 g/mol
PubChem SlD: 474492335
CAS Number:2381089-83-2
Synonyms:LY-3437943,NOP2Y096GV
Retatrutide is a cutting-edge triagonist peptide targeting three key metabolic receptors: GLP-1, GIP, and glucagon receptors. This multi-pathway approach enables profound appetite suppression, fat metabolism activation, and improved glucose regulation—positioning it as a highly promising therapeutic for obesity and metabolic disorders.
GLP-1 receptor agonism helps control appetite and slows gastric emptying, improving postprandial glucose control.
GIP receptor activation improves insulin secretion and may enhance pancreatic β-cell function.
Glucagon receptor stimulation boosts energy expenditure and facilitates lipid oxidation, contributing to significant fat loss
This synergistic activation leads to a comprehensive remodeling of metabolic processes, setting Retatrutide apart from single- or dual-pathway incretin agents.
Body Weight Reduction: In a pivotal placebo-controlled study, Retatrutide induced average weight loss of up to 24.2% at 48 weeks in individuals with obesity but no diabetes
Liver Fat Clearance: In metabolic dysfunction–associated steatotic liver disease (MASLD), up to 93% of participants achieved normalization of liver fat content, with an 82% reduction at 24 weeks
【https://www.nature.com/articles/s41591-024-03018-2】
Insulin Sensitivity: Improvement in HOMA-IR, fasting insulin, and HbA1c were consistently observed across all dosing levels
Triglycerides: Retatrutide lowered serum triglycerides by over 40% in high responders
Adipokines: Favorable shifts in leptin, adiponectin, and βhydroxybutyrate
Visceral & Subcutaneous Fat: Both compartments showed substantial reductions under MRI observation
💥 Superior weight-loss efficacy compared to existing GLP-1 or GIP agents
🧠 Central and peripheral action: appetite suppression + increased energy use
🔬 Triagonist model: activates 3 metabolic axes for maximal fat oxidation and hormonal balance
🩺 Liver and cardiovascular benefits: Reduces visceral fat, triglycerides, and liver steatosis
🌐 Potential applicability to obesity, T2D, MASLD/NASH, and cardiometabolic syndrome
Assessing the maintenance of weight loss after treatment cessation
Longitudinal monitoring of cardiovascular markers, adrenal hormones, and hepatic enzymes
Evaluating efficacy versus semaglutide, tirzepatide, and other dual agonists
Defining the ideal patient phenotype for triagonist therapy
New trials underway to examine kidney protection potential in obese and insulin-resistant populations
Studying effects in prediabetic, normoglycemic obese, and older adult groups
Application in PCOS, sleep apnea, and lipodystrophy syndromes
Oral peptide systems, microneedle patches, and slow-release injectables are being explored to increase compliance and absorption
Developing AI-based models to individualize dose titration based on fat distribution, insulin resistance, or liver biomarkers
Indication | Benefits |
Obesity / Overweight | Most significant body fat loss in clinical peptide research |
T2DM / Prediabetes | Improved glucose control, HbA1c, insulin sensitivity |
MASLD / NASH | Near-complete reversal of liver steatosis and reduced inflammation |
Cardiovascular Risk Management | Reduces triglycerides, visceral fat, and systolic blood pressure |
Metabolic Syndrome | Effective across multiple criteria: BMI, lipids, insulin resistance |
Weight Regain Prevention | Potential maintenance agent post-bariatric surgery or GLP-1 therapy |
Retatrutide represents a major advancement in metabolic peptide therapeutics. By simultaneously activating the GLP-1, GIP, and glucagon receptors, it delivers unprecedented weight loss, improved insulin sensitivity, and powerful liver-fat clearance—without relying on any single hormonal pathway. With broad indications spanning from obesity to MASLD and metabolic syndrome, Retatrutide is fast becoming one of the most promising agents in the fight against modern metabolic disease.
ALL ARTICLES AND PRODUCT INFORMATION PROVIDED ON THIS WEBSITE ARE FOR INFORMATONAL AND EDUCATIONAL PURPOSES ONLY.
The products offered on this website are furnished for in-vitro studies only. In-vitro studies(Latin: in glass) are performed outside of the body. These products are not medicines or drugs and have not been approved by the FDA to prevent, treat or cure any medical condition, ailment or disease. Bodily introduction of any kind into humans or animals is strictly forbidden by law.
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