Home / Retatrutide 5mg-120mg
  • Retatrutide 5mg-120mg
  • Retatrutide 5mg-120mg
  • Retatrutide 5mg-120mg
  • Retatrutide 5mg-120mg
  • Retatrutide 5mg-120mg
  • Retatrutide 5mg-120mg
  • Retatrutide 5mg-120mg
  • Retatrutide 5mg-120mg
  • Retatrutide 5mg-120mg
  • Retatrutide 5mg-120mg
  • Retatrutide 5mg-120mg

Retatrutide 5mg-120mg

The peptide will be provided as lyophilized powder to ensure maximum stability.
Retatrutid is an advanced research peptide studied for its unique activity involving GLP-1, GIP, and glucagon receptor pathways. As a triple receptor agonist, it has attracted significant attention in metabolic research, including studies related to energy balance, glucose metabolism, appetite regulation, and body weight mechanisms. The 60mg specification provides researchers with a suitable quantity for laboratory analysis, peptide research, and experimental evaluation.
$410
$512
Quantity
ADD TO CART
BUY IT NOW
  • Detail

    Research Peptide · For Laboratory Use Only

    Retatrutide 10mg

    Triple GIP/GLP-1/Glucagon Receptor Agonist · 39-Amino-Acid Fatty-Acid-Conjugated Peptide · Lyophilized Powder · Purity ≥99% (HPLC)

    Retatrutide (development code LY3437943) is a single-molecule triple hormone receptor agonist that simultaneously activates the GIP receptor (GIPR), the GLP-1 receptor (GLP-1R) and the glucagon receptor (GCGR) — the first peptide of its class to reach late-stage clinical development. Its 39-amino-acid backbone carries a distinctive set of stability modifications: two α-aminoisobutyric acid (Aib) residues that block DPP-4-type cleavage and an α-methyl-leucine (α-Me-Leu) that reinforces the helical pharmacophore against proteolysis. A C20 fatty diacid is conjugated to a lysine side chain through a hydrophilic γ-Glu-AEEA-AEEA linker, enabling reversible albumin binding and once-weekly pharmacokinetics.

    In clinical research, retatrutide has produced the largest body-weight reductions reported for any incretin-based therapy to date — up to approximately 24% at 48 weeks in Phase 2 and around 28% in Phase 3 trials — by combining appetite suppression (GLP-1R), insulin sensitization and lipid handling (GIPR), and glucagon-driven energy expenditure and hepatic fat oxidation (GCGR). Each vial is supplied as a sterile lyophilized (freeze-dried) powder to ensure maximum stability.

    Product Specifications

    Product Name Retatrutide (LY3437943)
    CAS Number 2381089-83-2
    Amino Acid Sequence H-Tyr-Aib-Gln-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Ile-αMeLeu-Leu-Asp-Lys-Lys(AEEA-AEEA-γ-Glu-C20 diacid)-Ala-Gln-Aib-Ala-Phe-Ile-Glu-Tyr-Leu-Leu-Glu-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Pro-Ser-NH₂ (39-residue backbone; Aib = α-aminoisobutyric acid; αMeLeu = α-methyl-leucine; C-terminal amide)
    Molecular Formula C₂₂₁H₃₄₂N₄₆O₆₈
    Molecular Weight 4731.33 Da (≈4.7 kDa)
    Receptor Profile Balanced triple agonist at GIPR, GLP-1R and GCGR (reported in vitro EC₅₀: GIPR ≈0.064 nM, GLP-1R ≈0.78 nM, GCGR ≈5.8 nM)
    Key Modifications Two Aib substitutions (DPP-4 resistance) · α-Me-Leu (protease resistance, helix stabilization) · C20 fatty diacid via γ-Glu-AEEA-AEEA linker (albumin binding, once-weekly PK)
    Quantity 10mg per vial
    Physical Form White to off-white lyophilized powder
    Purity ≥99% as determined by HPLC
    Storage -20°C for long term; 2–8°C for short term (lyophilized)

    What is Retatrutide?

    The incretin field has progressed in clear steps: selective GLP-1 agonists (semaglutide), then dual GIP/GLP-1 agonists (tirzepatide), and now triple agonists that add glucagon receptor activity to the mix. Retatrutide represents the third step — engineered on the premise that each of the three gut-pancreas hormones contributes a distinct and complementary metabolic effect, and that a single balanced molecule can engage all three pathways at once.

    The molecule was optimized for balanced triple activity through rational peptide design. Its key structural features include:

    • A 39-amino-acid single-chain backbone derived from the incretin pharmacophore, with residues tuned to maintain meaningful affinity at all three receptors within one sequence;
    • Two Aib residues, non-coded amino acids that block N-terminal peptidase (DPP-4-type) cleavage;
    • An α-methyl-leucine (α-Me-Leu) modification that stabilizes the helical conformation and further resists proteolytic degradation — a modification characteristic of next-generation incretin analogs;
    • A C20 fatty diacid on a lysine side chain attached through a γ-Glu-AEEA-AEEA hydrophilic linker, producing reversible albumin binding that extends the half-life to support once-weekly administration;
    • A C-terminal amide, completing the linear, non-cyclic design.

    In published research, retatrutide has been investigated in a wide range of settings, including:

    • Obesity research — the Phase 2 trial published in the New England Journal of Medicine reported dose-dependent weight reduction of up to approximately 24% at 48 weeks, the largest incretin-mediated effect reported at the time;
    • Type 2 diabetes — significant HbA1c reduction alongside weight effects in the same program;
    • Hepatic steatosis — early-phase data showed marked reductions in liver fat content, supporting ongoing studies in metabolic dysfunction-associated steatotic liver disease (MASLD/MASH);
    • Phase 3 TRIUMPH program — late-stage trials in obesity have reported weight reductions around 28%, extending the dose-response curve beyond dual agonists;
    • Receptor pharmacology and structure-activity studies — cryo-EM structural work has resolved how retatrutide simultaneously engages GLP-1R, GIPR and GCGR, making it a key reference compound for triple-agonist design.

    As the most advanced triple incretin agonist in clinical development, retatrutide has become the benchmark molecule for the next generation of metabolic therapies — a reference compound of central importance for laboratories studying coordinated GIP/GLP-1/glucagon signaling.

    Mechanism of Action

    1. GLP-1R Agonism — Appetite & Glycemic Control

    GLP-1 receptor activation drives glucose-dependent insulin secretion, suppresses glucagon in the fed state, delays gastric emptying and activates central anorexigenic pathways — the classic incretin contribution to reduced food intake and improved glycemic control.

    2. GIPR Agonism — Insulin Sensitization & Lipid Handling

    GIP receptor activation enhances the insulinotropic response to nutrients, improves insulin sensitivity and modulates adipose tissue lipid handling. Combined with GLP-1R activity, GIPR agonism is associated with improved tolerability and additive metabolic effects.

    3. GCGR Agonism — Energy Expenditure & Fat Oxidation

    The distinguishing third arm: glucagon receptor activation increases energy expenditure, promotes hepatic fatty acid oxidation and reduces liver fat — adding a caloric-expenditure component to the appetite-reduction effects of the incretin pathways.

    4. Balanced Triple Pharmacology

    Retatrutide was deliberately tuned for balanced rather than maximal activity at each receptor — sub-nanomolar to low-nanomolar potency across GIPR, GLP-1R and GCGR — a design choice intended to capture synergistic metabolic benefits while limiting glucagon-related glycemic liability.

    5. Albumin-Binding Pharmacokinetics

    The C20 fatty diacid moiety binds reversibly to plasma albumin, shielding the peptide from enzymatic degradation and renal clearance. The result is an extended elimination half-life compatible with once-weekly dosing — consistent with the design shared across modern lipidated incretin analogs.

    Handling & Storage Guidelines

    • Lyophilized powder: Store at -20°C for long-term stability; 2–8°C is acceptable for short-term storage. Avoid repeated temperature cycling and protect from light and moisture.
    • Before opening: Allow the vial to reach room temperature and briefly centrifuge to ensure the full contents collect at the bottom of the vial.
    • Reconstitution: Add bacteriostatic water or an appropriate solvent gently along the vial wall. Swirl slowly until fully dissolved; avoid vigorous shaking. As a lipidated amphipathic peptide, retatrutide may dissolve slightly slower than small peptides — patient, gentle swirling is recommended.
    • Reconstituted solution: Store at 2–8°C, protect from light, and use promptly; do not refreeze the solution.
    • General: Handle with standard laboratory protective equipment (gloves, lab coat, eye protection).

    Why Choose Our Retatrutide?

    🧪

    Verified Purity

    Each batch tested by HPLC & MS; COA available upon request.

    📦

    Secure Packaging

    Sealed vials with temperature-protective packaging for safe delivery.

    🚚

    Fast Dispatch

    Orders processed promptly with tracking provided.

    Frequently Asked Questions

    Q1: How is retatrutide different from tirzepatide and semaglutide?

    A: They represent three generations of incretin-based design. Semaglutide is a selective GLP-1 receptor agonist; tirzepatide adds GIP receptor activity (dual agonist); retatrutide adds glucagon receptor activity on top of both (triple agonist). The glucagon component contributes increased energy expenditure and hepatic fat oxidation — a mechanism absent from the first two generations — which is reflected in the larger weight reductions observed in clinical trials.

    Q2: Why does retatrutide contain the unusual modifications Aib and α-Me-Leu?

    A: Both are non-coded amino acids used to defeat enzymatic degradation. Aib (α-aminoisobutyric acid) blocks DPP-4-type cleavage near the N-terminus, while α-methyl-leucine stabilizes the helical pharmacophore and resists proteolysis. Together with the albumin-binding fatty acid chain, they enable the once-weekly pharmacokinetic profile.

    Q3: Isn't glucagon a blood-sugar-raising hormone — why agonize its receptor?

    A: This is a deliberate and much-studied design choice. In the context of concurrent GLP-1R and GIPR agonism (which strongly control glycemia), GCGR activation contributes increased energy expenditure, lipid oxidation and liver-fat reduction without the glycemic liability that unopposed glucagon would cause. Retatrutide's balanced receptor potencies were tuned specifically to capture this synergy.

    Q4: What is the development status of retatrutide?

    A: Retatrutide is an investigational compound in Phase 3 clinical trials (TRIUMPH program) for obesity, type 2 diabetes and liver-fat-related indications. It is not an approved pharmaceutical product anywhere for the purposes sold here.

    Q5: How should I store it after receiving?

    A: Keep unopened vials at -20°C for long-term storage. Once reconstituted, refrigerate at 2–8°C, protect from light, and use promptly; do not refreeze the solution.

    Q6: Is a Certificate of Analysis (COA) available?

    A: Yes, third-party tested COA documentation can be provided for each batch. Please contact our customer service with your order number.

    ⚠ Research Use Only — Disclaimer

    All product information provided on this page is solely for information dissemination and educational purposes. The products offered are intended exclusively for in vitro laboratory research and are not pharmaceuticals. They have not been approved by the U.S. Food and Drug Administration (FDA) or any other regulatory authority for the purposes sold here, and must not be used to prevent, treat or cure any medical condition, disease or ailment.

    It is strictly prohibited to introduce these products into the human or animal body in any form. By purchasing, the buyer acknowledges full responsibility for the proper handling, use and compliance with all applicable local laws and regulations.

  • Customer Reviews
    No comments