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Home > Pharmaceutical Intermediates > Bulk Drug Intermediates > Retatrutide for Sale > Retatrutide API Powder CAS 2381089-83-2 High Purity Peptide Raw Material
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Retatrutide API Powder CAS 2381089-83-2 High Purity Peptide Raw Material

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Unit Price:

$180/UNIT FOB

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CAS No.:

2381089-83-2

Grade:

Pharmaceutical Grade

Content:

99%

Port:

Hongkong

Brand:

Novio

Packaging:

1g/bottle,10g/bottle,100g/bottle

Sample Available:

Yes

Price valid (until):

2028-01-31

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

Peptides,Cosmetic Raw Materials,Pharmaceutical Intermediates

  • Product Details

  • Seller Information

  • Inquiry History

  • Description


      Product Detail  


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    Retatrutide is a synthetic peptide featuring a rationally designed sequence and chemical modifications. Functioning as an active agent that synergistically engages three receptors, it is supplied as a bulk lyophilized powder API and is widely used in scientific research involving *in vitro* models of metabolic homeostasis. Thanks to its unique molecular structure, the molecule simultaneously binds to three key receptor classes, triggering multiple downstream signaling pathways and synergistically regulating intracellular nutrient partitioning, lipid turnover, and energy metabolism. As a peptide API, Retatrutide exhibits excellent physicochemical stability; processed through multiple rounds of chromatographic purification, it ensures consistent and controllable batch quality. It serves as a reliable experimental substrate for investigating the mechanisms of triple-target metabolic molecules and screening active formulations—whether used in single-factor control experiments or in combination studies with other metabolic active ingredients—making it a highly significant material in current metabolic biology research.

    The core scientific attribute of Retatrutide lies in its synergistic regulation of metabolic homeostasis via three receptors. Intracellular nutrient storage, conversion, and consumption rely on a sophisticated dynamic equilibrium system. When the cellular metabolic environment shifts, nutrient substrates often undergo massive conversion and accumulate as lipids, leading to imbalances across multiple metabolic pathways. Upon binding to its target receptors, Retatrutide simultaneously activates downstream signaling cascades, remodeling cellular metabolic patterns through multiple routes, optimizing nutrient substrate partitioning, and mitigating sustained intracellular lipid accumulation. In *in vitro* cell culture models, the addition of Retatrutide at appropriate concentrations downregulates the transcriptional activity of genes associated with lipid synthesis, accelerates lipid oxidation and breakdown, and modulates the formation and consumption of intracellular lipid droplets, thereby helping to restore metabolic balance. Compared to single- or dual-target active peptides, this triple-receptor synergistic mode of action allows for intervention in metabolic processes across more dimensions, yielding more comprehensive regulatory effects—a key reason why this molecule remains a subject of intense investigation in metabolic research.

    Lipid metabolism remodeling is a major area of ​​research for Retatrutide. Lipids are stored within cells as lipid droplets, and the dynamic ratio between lipid synthesis and breakdown directly determines the level of intracellular lipid accumulation. Retatrutide modulates the expression levels of functional proteins associated with lipid metabolism; it inhibits the activity of lipid synthesis pathways while promoting lipid oxidative metabolism, thereby accelerating the conversion and consumption of stored lipids, reducing lipid droplet volume, and lowering intracellular lipid content. In high-fat-induced *in vitro* cell models, treatment with Retatrutide results in a significant decrease in total intracellular lipid content and an improvement in lipid metabolism-related markers. The regulatory effects of this peptide are concentration-dependent, with varying concentrations altering the intensity of metabolic regulation. Researchers can conduct experiments using concentration gradients to investigate the relationship between dosage and metabolic effects, thereby refining the study of the molecule's structure-activity relationship and providing a crucial reference for the future optimization of novel active molecules.

    Beyond lipid regulation, Retatrutide also participates in balancing cellular energy budgets and optimizing the energy conversion efficiency of nutrient substrates. Stable cellular energy metabolism relies on the coordinated operation of multiple biochemical pathways. When nutrient supply exceeds consumption demand, excess substrates are diverted toward lipid storage pathways. Through receptor-mediated signaling, Retatrutide upregulates energy expenditure pathways, enhances cellular energy turnover, and alters how cells utilize various nutrient substrates. This regulatory action reduces the conversion and storage of nutrients as lipids and directs substrates toward energy generation, thereby maintaining a dynamic balance in cellular energy. In long-term *in vitro* cell culture systems, Retatrutide demonstrates the ability to sustain its regulatory effects on metabolic signaling and alleviate cellular physiological abnormalities caused by metabolic imbalance.

    Regarding physicochemical properties, the bulk material is supplied as a lyophilized powder. The production and purification process adheres to standardized protocols, comprising sequential steps such as solid-phase peptide synthesis, chromatographic purification, filtration for impurity removal, and lyophilization/packaging. Product purity is assessed via High-Performance Liquid Chromatography (HPLC), with molecular structure verification performed using mass spectrometry. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing key metrics—such as purity, moisture content, impurities, and residual solvents—to facilitate quality verification by the purchaser. The lyophilized powder requires storage in a sealed, light-protected, and low-temperature environment to minimize the rate of molecular degradation and preserve biological activity over the long term. In *in vitro* experimental procedures, the lyophilized Retatrutide powder can be dissolved in suitable solvents to prepare stock solutions of varying concentrations; these are then diluted as needed and added to cell culture media. The Retatrutide solution demonstrates excellent compatibility with standard cell culture media; upon reconstitution, the liquid remains clear without significant precipitation. It introduces no irritating by-products and minimizes solvent-induced experimental interference, thereby ensuring high reproducibility of results and making it suitable for large-scale research projects.

    Lyophilized Retatrutide API powder supports a wide range of research applications across various branches of metabolic biology. First, in lipid metabolism modeling, it is used to establish *in vitro* cell systems for studying lipid accumulation. By setting up groups with concentration gradients, researchers can observe changes in lipid droplet morphology and intracellular lipid content following Retatrutide treatment, evaluate the peptide's regulatory effects on lipid metabolism pathways, and screen for novel multi-target active molecules. Second, regarding receptor signaling pathways, molecular interaction assays are employed to verify Retatrutide's binding affinity to target receptors, elucidate the operational logic of downstream signaling networks following receptor activation, and uncover the underlying mechanisms of the triple-target synergistic effect. Third, in the study of genes related to metabolic homeostasis, researchers measure changes in the transcriptional levels of metabolism-related genes and analyze the peptide's regulatory patterns on gene expression, thereby refining the understanding of metabolic molecular mechanisms. Fourth, in the development of peptide combination systems, Retatrutide is combined with other metabolic agents to investigate alterations in cellular metabolism resulting from the combined action of multiple active substances, facilitating the development of novel composite active formulations. Fifth, in parallel control experiments, Retatrutide is frequently compared with other metabolic-regulating peptides—such as Mazdutide, Tirzepatide, and Survodutide—to distinguish differences in activity regarding lipid metabolism and energy regulation among various multi-receptor agonist molecules.

    Retatrutide is a triple-receptor metabolic-regulating peptide. Compared to other peptides in this research field, it shares common research objectives while possessing distinct characteristics. Tirzepatide, a dual-receptor agonist peptide, also focuses on lipid metabolism and energy homeostasis and serves as a common control in parallel experiments; however, the two differ in molecular sequences, target combinations, and receptor affinity ratios, resulting in marked differences in regulatory potency within cell models. Mazdutide is a dual-receptor agonist peptide that focuses on activating lipid oxidation pathways; compared to Retatrutide, its signal regulatory network covers fewer dimensions. Survodutide features a different combination of therapeutic targets, offering unique advantages in lipolysis, though it lacks the metabolic regulatory effects mediated by a third receptor. AOD peptides also modulate intracellular lipolysis but do not function as receptor agonists, representing a fundamentally different mechanism of action. 5-Amino-1MQ primarily drives mitochondrial energy activation and enhances cellular metabolic turnover efficiency through pathways independent of receptor regulation. Researchers can use Retatrutide alone or in parallel with other metabolic peptides to analyze, from multiple perspectives, the underlying molecular mechanisms by which these active peptides regulate cellular metabolism.

    Rigorous control group design is essential for obtaining reliable data in *in vitro* cell experiments. Standard experimental setups require blank and vehicle control groups to rule out interference from the culture medium or the solvent itself. Additionally, establishing multiple concentration gradients allows for the plotting of dose-response curves and the identification of optimal working concentration ranges for the experimental model. Factors such as cell seeding density, incubation duration, and culture conditions (temperature and gas composition) influence the regulatory efficacy of the peptides. Preliminary experiments are necessary to optimize parameters, minimize data bias caused by extraneous variables, and ensure the stability and reproducibility of results in accordance with basic research standards. As these peptides exhibit dose-dependent effects—with excessively high concentrations imposing metabolic stress on cells—concentration screening is a critical step in experimental design.

    Consistent raw material quality is a prerequisite for the smooth execution of large-scale research projects. During industrial-scale production and purification, strict control over every processing step—including the removal of truncated peptides, residual solvents, and heavy metals—ensures consistent quality across batches. Reliable raw material quality prevents experimental irreproducibility caused by batch-to-batch purity variations, thereby saving time, consumables, and research funding. For research laboratories and biotechnology R&D companies, Retatrutide lyophilized API serves as a stable and reliable material for research in metabolic homeostasis, lipid biology, and peptide receptor signaling. Basic research on peptides continues to advance, with increasingly in-depth *in vitro* exploration of multi-target receptor-agonist peptides. Leveraging a unique molecular design that synergistically targets three receptors, Retatrutide exhibits multiple activities—including lipid remodeling, regulation of energy balance, and maintenance of metabolic homeostasis—thereby enriching the repertoire of research materials in the field of metabolism. This lyophilized API can serve as a standalone intervention agent for single-variable experiments or be used in combination with other research materials to investigate cellular metabolic dynamics under the influence of multiple active substances. Extensive *in vitro* cell experiments continue to refine the understanding of Retatrutide’s mechanism of action, driving progress in research regarding receptor signaling pathways, lipid metabolism regulation, and peptide structure-activity relationships. As a synthetic peptide research material available for bulk procurement, Retatrutide provides robust support for basic research in metabolic biology, helping scientists elucidate the molecular mechanisms underlying cellular metabolic regulation and fostering continued exploration in the development of multi-target active peptides.

    Items
    Specifications
    Product Name  Retatrutide
    Form Solid freeze-dried powder
    Storage condition -20°C
    Purity 99%
    Shop Retatrutide, Lyophilized powder, Triple-receptor agonist, Metabolic homeostasis, Lipid metabolism, Energy balance, Research API, In vitro cell study-Detailed Image 1
    Shop Retatrutide, Lyophilized powder, Triple-receptor agonist, Metabolic homeostasis, Lipid metabolism, Energy balance, Research API, In vitro cell study-Detailed Image 2
    Shop Retatrutide, Lyophilized powder, Triple-receptor agonist, Metabolic homeostasis, Lipid metabolism, Energy balance, Research API, In vitro cell study-Detailed Image 3
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    Shop Retatrutide, Lyophilized powder, Triple-receptor agonist, Metabolic homeostasis, Lipid metabolism, Energy balance, Research API, In vitro cell study-Detailed Image 10
    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 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
    7593 Inquiries
    Country Product Purchase Quantity Date Posted
    United States

    Retatrutide

    30 MG Nov 9, 2026
    Canada

    retatrutide

    20 MG Nov 9, 2026
    United States

    Retatrutide

    30 MG Nov 9, 2026
    United States

    retatrutide

    30 MG Nov 9, 2026
    United States

    retatrutide

    50 MG Nov 9, 2026
    Turkey

    retatrutide

    30 MG Nov 9, 2026
    United Kingdom

    Retatrutide

    100 MG Nov 9, 2026
    United States

    Retatrutide

    10 MT Nov 9, 2026
    United States

    Retatrutide

    60 MG Nov 9, 2026
    Canada

    Retatrutide

    20 MG Nov 9, 2026
    Australia

    Retatrutide

    1 MT Nov 8, 2026
    Australia

    Retatrutide

    1 MT Nov 8, 2026
    United States

    Retatrutide

    1 MT Nov 7, 2026
    Germany

    Retatrutide

    2 MT Nov 7, 2026
    Norway

    Retatrutide

    100 PCS Nov 7, 2026
    United States

    Retatrutide

    4 MT Nov 6, 2026
    Israel

    Retatrutide

    10 MT Nov 6, 2026
    Australia

    Retatrutide

    10 MG Nov 6, 2026
    United Kingdom

    Retatrutide

    100  Nov 6, 2026
    United States

    Retatrutide

    30 MG Nov 6, 2026
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