Lot #260601RT203

$80.00

Triple GIP/GLP-1/Glucagon Receptor Agonist (Retatrutide)

GLP-3 [20mg]

20mg / vial

Triple incretin receptor agonist

≥99% HPLC

4.9 / 5

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$80.00

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≥99% HPLC Purity

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Compound Profile

Researcher-grade specs. No guesswork.

Each vial ships with structural data and lot identifiers for the compound, plus a Certificate of Analysis documenting purity and identity. Ready for the bench. Synthesized via solid-phase peptide synthesis (SPPS), purified by reverse-phase HPLC, verified by mass spectrometry, and tested for sterility and endotoxin load. Every spec is documented on the signed Certificate of Analysis that ships with your vial.

— Component 01
Retatrutide · 20mg
Class
Triple GIP/GLP-1/Glucagon receptor agonist
Sequence
39 aa triple incretin receptor agonist with C18 fatty diacid modification (GIP/GLP-1/Glucagon triple agonist scaffold)
CAS Number
2381089-83-2
Molecular Formula
C₂₂₁H₃₄₂N₄₆O₆₈
Molecular Weight
4,731.34 g/mol
Per-component purity
≥ 98%
In the Literature

One compound. One research record.

Retatrutide is a 39-amino acid synthetic peptide that acts as a triple agonist at glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP), and glucagon (GCG) receptors.

The triple receptor agonism of retatrutide adds hepatic glucagon receptor activation to the incretin-based effects of dual GIP/GLP-1 agonists. Published research has examined hepatic fat oxidation, resting metabolic rate, and energy expenditure pathways associated with this triple-agonist mechanism in preclinical models.

This product is for laboratory research use only. Not for human administration. Not intended to diagnose, treat, cure, or prevent any disease.

For research use only. Statements above describe published research literature and do not constitute health, medical, or therapeutic claims for either compound or for the blend. Not for human or veterinary use. Not evaluated by the FDA.

Documented Research Areas

  • Triple GLP-1/GIP/glucagon receptor binding and co-activation in vitro
  • Hepatic fat oxidation and VLDL secretion modulation via glucagon receptor activation
  • Body weight and adiposity reduction in diet-induced obesity preclinical models
  • Energy expenditure and metabolic rate modulation in preclinical metabolic studies
  • Comparative triple versus dual incretin receptor agonism pharmacology

Selected Studies · Peer-Reviewed Literature

A curated list of published peer-reviewed papers indexed in PubMed where BPC-157 has been studied. Provided for research-context only. Linking to the literature does not constitute endorsement of any therapeutic application.

01

Jastreboff AM, et al. · N Engl J Med

Triple-Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial

PubMed · PubMed · 37366317
02

Rosenstock J, et al. · Lancet

Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes: a randomised, double-blind, placebo and active controlled phase 2 trial

PubMed · PubMed · 37366302

Compound database reference for chemical and structural data:

Transparency

Every lot. Every researcher. Same proof.

Each batch ships with a third-party Certificate of Analysis from BioRegen Analytical. HPLC purity, mass-spectrometry identity, sterility, and LAL endotoxin screening. Every test, every lot.

Your lot number ships on the label and on the COA. Enter it in the verifier any time to retrieve the original lab report.

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Certificate of Analysis

CompoundRetatrutide
CAS#2381089-83-2
FormulaC₂₂₁H₃₄₂N₄₆O₆₈
Mol. Weight4,731.34 g/mol
Identity (LC-MS)PASS
Purity (HPLC)99.75%
Sterility / LALPASS
Date Tested19 Jun 2026

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