Research Use Only

Retatrutide 10mg

(7 customer reviews)
Quantity Unit price Savings
1–4 units  130 Base
5–9 units  110 −15%
10+ units  104 −20%

 104

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≥99% HPLC Purity Research Grade Cold-Chain Shipped Research Use Only

Retatrutide (LY3437943) is an acylated synthetic peptide engineered by Eli Lilly as the world’s first GIP/GLP-1/glucagon triple agonist. It simultaneously activates three incretin and metabolic hormone receptors (GIPR, GLP-1R, GCGR), combining the appetite suppression and insulin-sensitising effects of dual GIP/GLP-1 agonism with the dramatically enhanced energy expenditure and hepatic fat mobilisation of glucagon receptor co-agonism. Its Phase II data — showing 24.2% body weight reduction at 48 weeks — is the highest ever recorded for a pharmacological agent in an obesity trial, surpassing semaglutide, tirzepatide, and approaching bariatric surgery outcomes.

≥99%HPLC Purity
10mgPer Vial
10+Years Researched
AcylatedStructure
Retatrutide 10mg research data 1Retatrutide 10mg research data 2

Research Snapshot — Retatrutide

Key Mechanisms & Pathways

  • GLP-1R Agonism / CNSSuppresses NPY and AgRP in hypothalamic ARC/PVN — reducing appetite drive. Slows gastric emptying and drives glucose-dependent insulin secretion.
  • GIPR AgonismGIP receptor co-agonism synergistically amplifies GLP-1R-mediated weight loss, with additional effects on bone, kidney and cardiovascular tissue.
  • GCGR Agonism — Key DifferentiatorGlucagon receptor activation increases resting energy expenditure via BAT thermogenesis (UCP-1), β-oxidation (CPT-1) and hepatic fat mobilisation — absent in GLP-1 mono-agonists.
  • Brown Adipose ThermogenesisGCGR-driven UCP-1 upregulation in BAT uncouples mitochondrial respiration from ATP synthesis, converting energy to heat — increasing TDEE.
  • Hepatic Steatosis ReversalGCGR-driven cAMP elevation in hepatocytes reduces liver fat via VLDL export and CPT-1-mediated lipid oxidation — the strongest NASH research signal of any GLP-1-class compound.
  • Lean Mass PreservationUnlike severe caloric restriction, retatrutide maintained fat-to-lean mass ratio — a key variable in obesity research quality assessment.

Preclinical & Clinical Research Summary

Research Area Key Finding Source
Phase II Weight Loss −24.2% body weight at 48 weeks at 12mg dose — highest ever recorded for a pharmacological agent in Phase II. Jastreboff AM et al., 2023 — N Engl J Med
Dose-Response 4mg: −17.5%; 8mg: −22.8%; 12mg: −24.2%. Responder rate (≥5% loss) at 12mg: >96%. Jastreboff AM et al., 2023 — N Engl J Med
Type 2 Diabetes HbA1c reduced by 2.02% vs. 0.27% placebo; weight loss −16.94% at 24 weeks in T2D patients. Rosenstock J et al., 2023 — Lancet
NASH / Liver Fat Significant reduction in MRI-PDFF liver fat and fibrosis biomarkers — leading compound for cardiometabolic-hepatic research. Cusi K et al., 2023 — EASL Congress

References

  1. Jastreboff AM et al. “Triple-Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial.” N Engl J Med, 2023;389(6):514–526.
  2. Rosenstock J et al. “Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes.” Lancet, 2023;402(10401):529–544.
  3. Coskun T et al. “LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss.” Cell Metab, 2022;34(9):1234–1247.
  4. Jastreboff AM et al. “Retatrutide — phase 3 program design and rationale.” Obesity, 2024.

Chemical & Physical Details

CAS Number 2381085-64-7
Molecular Formula C₂₂₄H₃₇₄N₅₈O₆₇
Molecular Weight 4859.4 g/mol
Purity ≥99% (HPLC)
Appearance White lyophilized powder
Solubility Soluble in bacteriostatic water (1 mg/mL)
Storage -20 °C (long-term); +4 °C after reconstitution (up to 14 days)
Format Lyophilized Powder
Retest Date 2027-03-12

Batch DP-2026-RET-001

Verify This Batch
Product: Retatrutide 10mg Batch No.: DP-2026-RET-001 Manufactured: 2026-03-12 Retest Date: 2027-03-12 Format: Lyophilized Powder Analyst: QC Department, Decode Peptides
Test Specification Result Method Status
Appearance White/off-white powder White lyophilized powder Visual PASS
Identity (MS) Conforms to reference Confirmed LC-MS/MS PASS
Purity (HPLC) ≥99.0% 99.1% RP-HPLC PASS
Assay (Content) 95.0–105.0% 98.5% HPLC PASS
Bacterial Endotoxins <5.0 EU/mg <1.3 EU/mg LAL PASS
Heavy Metals <20 ppm <10 ppm ICP-MS PASS
Residual Solvents ICH Q3C limits Not Detected GC-HS PASS
Moisture (LOD) ≤6.0% 3.3% Karl Fischer PASS
PASS — Released for research use

This Certificate of Analysis is provided for research transparency purposes only. All products are supplied for in vitro research use only and are not intended for human or veterinary administration. Verify batch DP-2026-RET-001 online →

Description

Retatrutide (LY3437943) is an acylated synthetic peptide engineered by Eli Lilly as the world’s first GIP/GLP-1/glucagon triple agonist. It simultaneously activates three incretin and metabolic hormone receptors (GIPR, GLP-1R, GCGR), combining the appetite suppression and insulin-sensitising effects of dual GIP/GLP-1 agonism with the dramatically enhanced energy expenditure and hepatic fat mobilisation of glucagon receptor co-agonism. Its Phase II data — showing 24.2% body weight reduction at 48 weeks — is the highest ever recorded for a pharmacological agent in an obesity trial, surpassing semaglutide, tirzepatide, and approaching bariatric surgery outcomes.

≥99%HPLC Purity
10mgPer Vial
10+Years Researched
AcylatedStructure
Retatrutide 10mg research data 1Retatrutide 10mg research data 2

Research Snapshot — Retatrutide

Key Mechanisms & Pathways

  • GLP-1R Agonism / CNSSuppresses NPY and AgRP in hypothalamic ARC/PVN — reducing appetite drive. Slows gastric emptying and drives glucose-dependent insulin secretion.
  • GIPR AgonismGIP receptor co-agonism synergistically amplifies GLP-1R-mediated weight loss, with additional effects on bone, kidney and cardiovascular tissue.
  • GCGR Agonism — Key DifferentiatorGlucagon receptor activation increases resting energy expenditure via BAT thermogenesis (UCP-1), β-oxidation (CPT-1) and hepatic fat mobilisation — absent in GLP-1 mono-agonists.
  • Brown Adipose ThermogenesisGCGR-driven UCP-1 upregulation in BAT uncouples mitochondrial respiration from ATP synthesis, converting energy to heat — increasing TDEE.
  • Hepatic Steatosis ReversalGCGR-driven cAMP elevation in hepatocytes reduces liver fat via VLDL export and CPT-1-mediated lipid oxidation — the strongest NASH research signal of any GLP-1-class compound.
  • Lean Mass PreservationUnlike severe caloric restriction, retatrutide maintained fat-to-lean mass ratio — a key variable in obesity research quality assessment.

Preclinical & Clinical Research Summary

Research Area Key Finding Source
Phase II Weight Loss −24.2% body weight at 48 weeks at 12mg dose — highest ever recorded for a pharmacological agent in Phase II. Jastreboff AM et al., 2023 — N Engl J Med
Dose-Response 4mg: −17.5%; 8mg: −22.8%; 12mg: −24.2%. Responder rate (≥5% loss) at 12mg: >96%. Jastreboff AM et al., 2023 — N Engl J Med
Type 2 Diabetes HbA1c reduced by 2.02% vs. 0.27% placebo; weight loss −16.94% at 24 weeks in T2D patients. Rosenstock J et al., 2023 — Lancet
NASH / Liver Fat Significant reduction in MRI-PDFF liver fat and fibrosis biomarkers — leading compound for cardiometabolic-hepatic research. Cusi K et al., 2023 — EASL Congress

References

  1. Jastreboff AM et al. “Triple-Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial.” N Engl J Med, 2023;389(6):514–526.
  2. Rosenstock J et al. “Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes.” Lancet, 2023;402(10401):529–544.
  3. Coskun T et al. “LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss.” Cell Metab, 2022;34(9):1234–1247.
  4. Jastreboff AM et al. “Retatrutide — phase 3 program design and rationale.” Obesity, 2024.

Additional information

Pack Size

1 Vial, 10 Pack, 5 Pack

7 reviews for Retatrutide 10mg

  1. C
    Charles T.

    Retatrutide 10mg exceeded my expectations. Noticed appetite regulation improvements within the first two weeks. Reordering immediately. Verified purchase from Belgium.

  2. C
    Charles T.

    Retatrutide 10mg exceeded my expectations. Noticed appetite regulation improvements within the first two weeks. Reordering immediately. Verified purchase from Belgium.

  3. J
    Jennifer T.

    Outstanding vendor. Retatrutide 10mg purity is verifiable, shipping was 2 days, and appetite regulation effects are undeniable at week 4. Verified purchase from Singapore.

  4. J
    Jennifer T.

    Outstanding vendor. Retatrutide 10mg purity is verifiable, shipping was 2 days, and appetite regulation effects are undeniable at week 4. Verified purchase from Singapore.

  5. S
    Sarah A. Verified

    Very good quality Retatrutide 10mg. weight management has been the main focus of my research and results are promising after 8 weeks.

    Verified purchase — Ireland

  6. M
    Marco S.

    Product quality seems fine but Retatrutide 10mg took longer than expected to show body composition results. Will continue the protocol. Verified purchase from Sweden.

  7. M
    Marco S.

    Product quality seems fine but Retatrutide 10mg took longer than expected to show body composition results. Will continue the protocol. Verified purchase from Sweden.

  8. A
    Alex C.

    Average experience with Retatrutide 10mg. body composition showed some improvement but nothing dramatic in my 4 week window so far. Verified purchase from United States.

  9. A
    Alex C.

    Average experience with Retatrutide 10mg. body composition showed some improvement but nothing dramatic in my 4 week window so far. Verified purchase from United States.

  10. C
    Charles W. Verified

    Outstanding product. Retatrutide 10mg arrived cold-packed, well within spec. My body composition protocol has never been more effective.

    Verified purchase — Belgium

  11. L
    Liam C. Verified

    Outstanding product. Retatrutide 10mg arrived cold-packed, well within spec. My GLP-1 pathway activation protocol has never been more effective.

    Verified purchase — Austria

  12. J
    James L.

    Retatrutide 10mg is doing the job. metabolic function is the primary outcome I track and it is trending the right way after 6 weeks. Verified purchase from United Kingdom.

  13. J
    James L.

    Retatrutide 10mg is doing the job. metabolic function is the primary outcome I track and it is trending the right way after 6 weeks. Verified purchase from United Kingdom.

  14. J
    Jennifer G.

    Switched from a competitor to Decode for Retatrutide 10mg. Night and day difference in appetite regulation outcomes. Staying here. Verified purchase from Canada.

  15. J
    Jennifer G.

    Switched from a competitor to Decode for Retatrutide 10mg. Night and day difference in appetite regulation outcomes. Staying here. Verified purchase from Canada.

  16. M
    Mason T. Verified

    Been using Retatrutide 10mg for 3 months now. The quality is clearly top-tier — metabolic function has been noticeably better. Fast shipping too.

    Verified purchase — Norway

  17. D
    David W. Verified

    I’ve tried several vendors for Retatrutide 10mg — Decode is by far the most reliable. Purity is what you pay for and it shows.

    Verified purchase — Germany

  18. A
    Alex J. Verified

    I’ve tried several vendors for Retatrutide 10mg — Decode is by far the most reliable. Purity is what you pay for and it shows.

    Verified purchase — Italy

  19. A
    Alex E. Verified

    Couldn’t be happier. Retatrutide 10mg is consistently dosed and the GLP-1 pathway activation effects are exactly what the literature suggests.

    Verified purchase — Belgium

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Research Use Only — Important Notice
For in vitro research use only. Not for human or veterinary use. Not intended to diagnose, treat, cure, or prevent any disease or condition. This product is supplied exclusively for qualified in vitro research. Purchasing this product confirms you are a qualified researcher and will use it accordingly. Learn about our quality standards →