RETATRUTIDE 20 MG Peptide
- ≥99% purity by HPLC
- Janoshik COA with every lot
- Lot-traceable from synthesis
- EU-synthesised
Specifications
Third Party Lab Tested
Every lot is independently HPLC-tested by Janoshik Analytical, Europe's reference laboratory for peptide purity assessment. The COA shipped with your order is theirs, not ours.
Storage & Handling
Lyophilized peptides should be stored below 16°C, protected from light and moisture, for up to 24 months. Once reconstituted, refrigerate and use within 30 days for protocol consistency.
Reconstitution
Reconstitute with bacteriostatic water using the volumes below. Add solvent slowly along the inside wall of the vial. Swirl gently, never shake, until fully dissolved.
Lab-handling protocol BAC Water · 0.9% benzyl alcohol The reconstitution solvent referenced above. Add to order →The triple agonist frontier.
Retatrutide is an investigational 39-amino-acid peptide characterised as a triple receptor agonist with binding activity at GLP-1R, GIPR and GCGR. This receptor profile distinguishes Retatrutide from single- and dual-pathway incretin analogues: the added glucagon-receptor component introduces a third metabolic signalling axis that published research associates with hepatic energy expenditure and lipid handling. Investigators study the Retatrutide peptide in metabolic and receptor-pharmacology models.
This 20 MG Retatrutide peptide is supplied as a lyophilized research vial within the NZM-Labs peptide line and is intended for laboratory research only. Independent analysis establishes HPLC purity and confirms mass-spectrometry identity for every production lot. Lot-specific documentation accompanies each vial and remains accessible through our Science page, so researchers can match the vial in hand to its own analytical record.
| Compound | Retatrutide |
|---|---|
| Sequence length | 39 amino acids |
| Molecular mass | 4731.2 Da |
| Modeled half-life | ~6 days (modeled) |
| Mechanism / research class | GLP-1R / GIPR / GCGR agonist |
| Example laboratory preparation | 4 mL bacteriostatic water (0.9% benzyl alcohol) |
| Calculated concentration | 5 mg per 1.0 mL |
| Supply format | Retatrutide · 20 MG lyophilized research vial |
| Storage, lyophilized | Store below 16°C for up to 24 months |
| Storage, reconstituted | Refrigerate and use within 30 days |
Synthesised.
Verified.
Documented.
Backed by research.
Measured in results.
Each tag opens the cited literature behind that effect. References are linked to PubMed.
Retatrutide is the first reported GLP-1 / GIP / glucagon triple agonist in published research. The added GCGR activation engages hepatic energy expenditure and lipolysis on top of the dual incretin profile, producing a steeper body-weight response than dual agonists in head-to-head reference trials.
Phase 2 trial reported −24.2% mean body-weight reduction at 48 weeks in the highest published study arm.
- Jastreboff AM et al. Triple-hormone-receptor agonist retatrutide for obesity - a phase 2 trial. NEJM. 2023;389(6):514-526. PubMed ↗
The triple-agonist mechanism is particularly active on hepatic lipid handling. The Retatrutide MASLD substudy reported up to 86% relative liver-fat reduction at 48 weeks - the steepest reduction reported for any incretin analog to date.
- Sanyal AJ et al. Triple agonist retatrutide on MASLD in a phase 2a substudy. Nat Med. 2024;30:2037-2048. PubMed ↗
GCGR engagement adds hepatic energy-expenditure modulation to the response envelope. Research populations show improvements on HOMA-IR and broader insulin-sensitivity markers consistent with the triple-pathway profile.
- Sanyal AJ et al. Nat Med. 2024;30:2037-2048. PubMed ↗
Despite GCGR activation (which can theoretically raise hepatic glucose output), net glycemic effect in research populations remains strongly negative - A1C reductions of 1.7–2.0% reported in the phase 2 trial across the higher dose arms.
- Rosenstock J et al. Retatrutide in T2D. The Lancet. 2023;402(10401):529-544. PubMed ↗
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