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Home > Pharmaceutical Intermediates > Bulk Drug Intermediates > Retatrutide for Sale > Retatrutide (LY3437943) API powder, CAS 2381089-83-2, high-purity peptide raw material.
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Retatrutide (LY3437943) API powder, CAS 2381089-83-2, high-purity peptide raw material.

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Unit Price:

$41/UNIT FOB

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CAS No.:

2381089-83-2

Grade:

Research Grade

Content:

99%

Port:

Hongkong

Brand:

Novio

Packaging:

5 mg 10 vials 10 mg 10 vials 15 mg 10 vials 20 mg 10 vials 30 mg 10 vials 40 mg 10 vials 50 mg 10 vials 60 mg 10 vials

Price valid (until):

2026-10-17

Company Type:
Trader
Location:
China
Qualification:
Main Products:

Peptides,Cosmetic Raw Materials,Pharmaceutical Intermediates

  • Product Description

  • Seller Information

  • Inquiry History

  • Description


      Product Detail  


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    Retatrutide is an innovative triple-receptor agonist developed by a globally renowned pharmaceutical company, representing a benchmark bioactive molecule in the evolution of metabolic science. Unlike traditional agents that target only one or two metabolic pathways, this molecule simultaneously activates three key metabolic receptors—GLP-1, GIP, and glucagon—creating a synergistic, multi-pathway regulatory system that comprehensively optimizes the body's metabolic processes. Leveraging unique molecular structural optimization, it offers core advantages such as high potency, versatility, and sustained efficacy. Its groundbreaking regulatory capabilities have made it a focal point in research on chronic metabolic conditions—including obesity, glucose metabolism disorders, and metabolic liver diseases—with extensive clinical trials confirming its exceptional value as a comprehensive therapeutic agent.

    The molecule's core strength lies in its precise, synergistic multi-pathway regulatory mechanism; the three metabolic pathways function both independently and complementarily, overcoming the limitations inherent in traditional, single-target metabolic therapies. Activation of the GLP-1 receptor optimizes digestive pacing and slows gastric emptying, prolonging satiety and fundamentally reducing excess caloric intake, thereby preventing the metabolic strain associated with overeating and frequent snacking. The GIP receptor sensitively detects fluctuations in glucose levels, dynamically regulating the efficiency of glucose conversion and utilization; it accelerates energy conversion during hyperglycemia and maintains metabolic homeostasis when levels are stable, preventing drastic fluctuations and solidifying the foundation of glucose balance. Meanwhile, the glucagon receptor targets energy output, effectively activating lipolysis, enhancing basal metabolic efficiency, and accelerating the expenditure of excess energy to minimize long-term lipid accumulation, thus achieving an integrated regulatory loop encompassing intake, utilization, and expenditure.

    Regarding the regulation of glucose homeostasis, Retatrutide exhibits highly intelligent regulatory characteristics, successfully balancing safety and efficacy. Its regulatory action is strictly glucose-dependent, activating potent regulatory mechanisms only when glucose levels exceed normal thresholds; it facilitates the rapid transport, absorption, and conversion of glucose—transforming excess sugar into usable energy—to effectively normalize hyperglycemic states. When blood sugar levels are within the standard range, the molecule avoids excessive intervention, effectively mitigating the risk of metabolic imbalance and ensuring the natural functioning of the metabolic system. Extensive clinical data indicate that long-term intervention significantly optimizes glycated hemoglobin (HbA1c) levels, drastically narrows the amplitude of blood sugar fluctuations, and fundamentally rectifies chronic glucose metabolic disorders. For individuals with complex metabolic issues, the molecule simultaneously improves both glucose and lipid metabolism; it breaks the vicious cycle wherein various metabolic abnormalities exacerbate one another, helping multiple key metabolic markers shift toward ideal ranges.

    In the realm of weight and body fat management, Retatrutide demonstrates superior efficacy compared to traditional agents, standing out as one of the most potent molecules for fat reduction and weight control currently under metabolic research. Leveraging a triple-pathway, bidirectional regulatory mechanism, it achieves three simultaneous effects—curbing intake, boosting energy expenditure, and reducing fat accumulation—thereby precisely targeting the root causes of weight imbalance. By prolonging satiety, it naturally lowers total daily food intake and reduces cravings for high-calorie, high-fat foods, effectively cutting off excess calorie accumulation at the source. Simultaneously, it elevates basal metabolic rates and accelerates the catabolism of excess subcutaneous and visceral lipids, specifically targeting fat deposits in critical areas. Long-term clinical trials show that systematic intervention leads to substantial overall weight loss and a significant reduction in visceral fat, alongside improvements in key body composition metrics such as waist circumference and body fat percentage. Unlike weight fluctuations caused by short-term water loss, its weight and fat reduction effects focus on optimizing adipose tissue, resulting in stable improvements to body composition and physical health.

    Beyond its core function of regulating glucose and lipid metabolism, Retatrutide offers exceptional systemic metabolic optimization. It addresses various sub-health issues stemming from metabolic dysfunction across multiple dimensions, thereby safeguarding the health of vital organs and the circulatory system. Regarding liver health, the molecule efficiently clears excess lipid deposits, alleviates the burden of hepatic fat accumulation, ameliorates hepatic steatosis, and restores disordered hepatic metabolic functions, offering a novel therapeutic pathway for metabolic-associated liver conditions. Furthermore, it comprehensively optimizes the body's lipid profile by effectively lowering levels of harmful lipids—such as triglycerides and low-density lipoproteins (LDL)—while increasing the proportion of beneficial lipoproteins. This reduces lipid deposition in the circulatory system, alleviates metabolic stress on the circulation, and lowers the likelihood of various metabolic complications. Numerous trials have observed that improvements in lipid and glucose markers are accompanied by beneficial changes in blood pressure-related indicators, further demonstrating the molecule's regulatory role in the overall metabolic environment.

    Retatrutide also effectively addresses various secondary issues arising from metabolic imbalance. Chronic metabolic disorders and excess body fat increase the physical load on the body, potentially leading to strain and sleep disturbances. By systematically optimizing metabolic function and reducing excess fat accumulation, the drug alleviates physical strain and wear-and-tear caused by chronic weight-bearing stress; simultaneously, it resolves sleep disturbances linked to metabolic abnormalities, helping to restore normal sleep patterns. This systemic, inside-out regulation optimizes both physical health and lifestyle, achieving a comprehensive improvement in metabolic well-being.

    Regarding its application characteristics, Retatrutide has undergone precise molecular optimization to ensure long-lasting, stable efficacy. Its optimized molecular structure extends the half-life, allowing for sustained activity across three key metabolic pathways and maintaining consistent regulatory effects. This significantly reduces the need for frequent dosing, making it highly suitable for long-term health management. Additionally, the R&D team has precisely balanced the activation intensity across these three receptors to achieve dynamic equilibrium; this approach mitigates the limitations of targeting a single pathway and avoids the risks of metabolic fluctuation, ensuring a regulatory effect that is both gentle and highly efficient.

    In terms of safety, current clinical trial data indicate that Retatrutide is well-tolerated. Adverse reactions are predominantly mild, transient gastrointestinal responses—often dose-dependent—that gradually resolve on their own as treatment progresses, with no evidence of persistent or severe adverse risks. The research team continues to monitor long-term data, tracking organ function, metabolic markers, and tolerability to further substantiate the clinical evidence. It is important to note that this substance remains in the clinical research stage and has not yet received regulatory approval for marketing in various regions; all observed effects stem from experimental settings and cannot replace fundamental lifestyle management, such as dietary control and exercise.

    From an industry perspective, Retatrutide marks a new phase in metabolic regulation research characterized by multi-target synergy. Many past interventions targeted only single biomarkers, making it difficult to address complex, multifactorial chronic conditions like metabolic syndrome. By integrating appetite regulation, glucose utilization, and energy expenditure, this molecule aligns with the underlying mechanisms of complex metabolic imbalances. Naturally, numerous questions require further investigation—such as long-term comprehensive performance, the sustainability of results after the intervention ends, and efficacy variations across different age groups and metabolic profiles—all of which must be addressed in subsequent trials. Future research will expand into additional areas, exploring the molecule's potential value in modulating chronic inflammation and other processes. Overall, through its multi-pathway synergistic mechanism, Retatrutide delivers multiple benefits—including improved glucose metabolism, body fat management, and metabolic protection for organs—thereby opening new avenues for research into chronic metabolic issues and providing a vital reference for the future development of metabolic therapies.

    Product name

    Retatrutide

    CAS NO.

    2381089-83-2

     Purity

    99%

    Molecular weight

    4731.33

    Appearance

    White powder

    Molecular Formula

    C221H342N46O68

    Specifications

    Frozen

    Function

    Weight loss

    Storage

    Storage

    Function

    Weight loss

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    ECHEMI Editorial Reference
    Retatrutide is a novel triple agonist peptide of the glucagon receptor (GCGR), glucose-dependent insulinotropic polypeptide receptor (GIPR) and glucagon-like peptide-1 receptor (GLP-1R). Retatrutide inhibits human GCGR, GIPR and GLP-1R with EC50 values of 5.79, 0.0643 and 0.775 nM, respectively and mouse GCGR, GIPR, and GLP-1R with EC50 values of 2.32, 0.191 and 0.794 nM, respectively. It is an important tool for obesity research.Retatrutide potently activates the GLP-1R signaling pathway to stimulate glucose-dependent insulin secretion through activity at the GIP receptor (GIPR) or the GLP-1R.Retatrutide is a synthetic peptide with glucose-lowering effects. It is an antidiabetic agent against type 2 diabetes (T2D), stimulating insulin and suppressing glucagon secretion in a glucose-dependent manner.Retatrutide was also shown to delay gastric emptying, lower fasting and postprandial glucose concentration, decrease food intake and reduce body weight in patients with type 2 diabetes.
    Retatrutide (LY-3437943) was discovered by the American pharmaceutical company Eli Lilly and Company. It is a triple glucagon hormone receptor agonist (GLP-1, GIP, and GCGR receptors) for obesity. The 2024 Lasker~DeBakey Clinical Medical Research Award has been given to Joel Habener and Svetlana Mojsov for their discovery of a new hormone GLP-1(7-37) and to Lotte Knudsen for her role in developing sustained acting versions of this hormone as a treatment for obesity.

    Certificates
    • Retatrutide (LY3437943) API powder, CAS 2381089-83-2, high-purity peptide raw material. Certificates 1 TDS

    Basic Info
    Product Name:

    Retatrutide

    Other Name:

    Retatrutide;GIPR/GLP-1R;LY3437943Retatrutide;Retalutide;Retatrutide (sodium salt);Retatrutide RT5;retatrutide 5mg;Retatratide

    CAS No.:

    2381089-83-2

    InChIKeys:

    MLOLQJNKXBNWFW-SAGGEDDASA-N

    Molecular Weight:

    0

    EC Number:

    200-001-8

    Color/Form:

    White lyophilized

    Characteristics
    Water Solubility:

    Soluble in water (5mg/ml).

    Storage Conditions:

    -20°C

    Critical Temperature & Pressure:

    -20°C

    Research
    Class:

    Triple agonist — GCGR, GIPR, GLP-1R

    Status:

    Investigational (Phase 3)

    Mechanism:

    Simultaneously activates glucagon receptor (GCGR), glucose-dependent insulinotropic polypeptide receptor (GIPR), and glucagon-like peptide-1 receptor (GLP-1R). Engineered from the native GIP backbone with amino acid substitutions to confer GCGR and GLP-1R activity.

    EC50 (Human GCGR):

    5.79 nM

    EC50 (Mouse GIPR):

    0.191 nM

    EC50 (Mouse GLP1R):

    0.794 nM

    EC50 (Mouse GCGR):

    2.32 nM

    EC50 (Human GLP1R):

    0.775 nM

    EC50 (Human GIPR):

    0.0643 nM

    Source:

    Jastreboff AM, et al. N Engl J Med. 2023;389(6):514-526.DOI

    Clinical Development:

    NCT04881760; NCT05882045; NCT06354660

    References
    ChEMBL:

    CHEMBL5095485

    DrugBank:

    DB18993

    KEGG DRUG:

    D12430

    PubChem:

    PubChem

    Disclaimer:

    Retatrutide is an investigational compound not yet approved by FDA or EMA. This listing is for industrial and laboratory research use only. Product information on ECHEMI is provided for sourcing and specification reference. It is not medical advice, a clinical recommendation, or an approved therapy description. Always verify regulatory status, purity, and intended use with the supplier and applicable authorities before purchase or use.

  • Seller Information
    Business Type:

    Trader

    Main Products:

    Peptides,Cosmetic Raw Materials,Pharmaceutical Intermediates

    Location:

    Room 1359, Room 103, Building Jia 19, Jixiang Garden, Tongzhou District, Beijing

    Year of Establishment:

    2026

  • Inquiry History
    7023 Inquiries
    Country Product Purchase Quantity Date Posted
    United States

    Retatrutide 2381089-83-2

    3 MT Mar 28, 2026
    United Kingdom

    Retatrutide - 2381089-83-2

    1 G Feb 10, 2026
    United States

    Retatrutide CAS 2381089-83-2 10mg vial

    20 MT Mar 7, 2026
    United States

    Factory Retatrutide API 99% Purity CAS 2381089-83-2

    5 KG Nov 10, 2025
    United Kingdom

    Peptide powder Retatrutide 99% pure for Body building cas 2381089-83-2 Weight Loss Peptide with COA

    1 MT Mar 22, 2026
    United States

    2381089-83-2

    100 G Jul 14, 2026
    United States

    2381089-83-2

    100 G Feb 24, 2026
    United States

    2381089-83-2

    100 MT Dec 9, 2023
    United States

    Retatrutide 2381089-83-2

    200 MG May 16, 2026
    United Kingdom

    2381089-83-2 retatrutide

    300 MG Feb 13, 2026
    United States

    Retatrutide 2381089-83-2 wholesale

    500 MT Nov 3, 2023
    United States

    Retatrutide CAS 2381089-83-2 99%

    10 PCS Feb 21, 2026
    Poland

    CAS 2381089-83-2 (Custom Peptide)

    40 MT Apr 10, 2026
    Austria

    Peptide Retatruide CAS 2381089-83-2

    100 MT Apr 4, 2026
    Austria

    Retatrutide CAS 2381089-83-2 10mg vial

    20 PCS Feb 10, 2026
    United States

    GLP-1 / GIP Retatrutide cas 2381089-83-2

    1 MT Oct 16, 2024
    United States

    Retatrutide 99% High Quality CAS 2381089-83-2

    1 G Jan 23, 2026
    United States

    Injection Peptide Tirzepatide/Retatrutide/ Semaglutide Peptides CAS 2381089-83-2

    10  Oct 21, 2023
    Australia

    GMP Grade 99% Retatrutide Lyophilized Powder CAS 2381089-83-2

    10 G Jun 12, 2026
    Palestine

    Factory 99% Purity Retatrutide Peptide CAS 2381089-83-2 Door-To-Door Service

    10 MG Mar 16, 2026
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