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GLP-3 (Retatrutide) research material
Vial · Research materialHelio®
Metabolic Research

GLP-3 (Retatrutide)

Retatrutide (development code LY3437943), marketed by the client as "GLP-3," is a synthetic single-molecule peptide of 39 amino acids engineered as a first-in-class triple incretin receptor agonist. In experimental characterization it activates three class B G-protein-coupled receptors simultaneously: the glucose-dependent insulinotropic polypeptide receptor (GIPR), the glucagon-like peptide-1 receptor (GLP-1R), and the glucagon receptor (GCGR). Its backbone incorporates aminoisobutyric acid (Aib) substitutions and fatty-acid acylation designed to confer protease resistance and extended circulating half-life.

In preclinical and in-vitro research, retatrutide has been used to study the pharmacology of combined incretin and glucagon-receptor engagement, including effects on energy metabolism, glucose handling, and adiposity in animal models. Its balanced triple-agonist profile distinguishes it from single (GLP-1R) and dual (GIP/GLP-1) agonists and has made it a subject of intense metabolic-research interest. This material is supplied strictly for Research Use Only.

Identification
  • MaterialGLP-3 (Retatrutide)
  • Research AreaMetabolic
  • PresentationVial
  • Available Sizes5mg · 10mg · 15mg · 30mg
  • CAS Number2381089-83-2
  • Molecular FormulaC221H342N46O68
  • Molecular Weight4731.34 g/mol
  • TypeSynthetic acylated peptide (triple incretin agonist)
  • Receptor / TargetGIP receptor (GIPR), GLP-1 receptor (GLP-1R), and glucagon receptor (GCGR)
  • PubChem CID171934787 →
Amino Acid Sequence

Y-Aib-QGTFTSDYSILLDKKAQ-Aib-AFIEYLLEGGPSSGAPPPS (39 residues, dual fatty-acid acylated)

Analytical Data
  • Purity (HPLC)≥99%
  • Identity (MS)Confirmed to specification
  • TestingAccredited (ISO 17025) third-party laboratory
  • CertificateView COA · Lot 26109001 →
From$69.95 – $149.95

Research use only — not for human or animal consumption. Per-batch documentation is provided with the material.

Key Characteristics
Molecular FormulaC221H342N46O68
Molecular Weight4731.34 g/mol
CAS Number2381089-83-2
PubChem CID171934787
Receptor / TargetGIPR, GLP-1R, and GCGR (triple agonist)
Molecular TypeSynthetic 39-residue acylated peptide
FormLyophilized powder in vial
SolubilitySoluble in water and bacteriostatic water; aliquot after reconstitution
StorageStore lyophilized at -20 C to -80 C; protect from light
StabilityLyophilized stable for extended periods frozen; reconstituted solutions less stable, use promptly
Research Context
Triple incretin receptor pharmacologyReference ligand for combined GIPR / GLP-1R / GCGR activation and signaling studies.
Energy metabolism researchModel compound for preclinical study of energy expenditure and adiposity.
Glucose homeostasisUsed in animal and cell-based models of glucose handling and insulin secretion.
Long-acting peptide designIllustrates Aib substitution and fatty-acid acylation strategies for half-life extension.
Research Findings

Published preclinical and early-phase research characterizes retatrutide as a balanced agonist across GIPR, GLP-1R, and GCGR, with in-vitro potency data reported for each receptor. In animal models it has been associated with changes in body weight, food intake, and glucose parameters attributed to its combined incretin and glucagon-receptor activity.

These observations derive from experimental, preclinical, and early clinical-pharmacology settings and are provided for scientific context only. No human efficacy, dosing, or therapeutic conclusions are implied by this listing.

History

Retatrutide (LY3437943) was developed by Eli Lilly as a triple GIP/GLP-1/glucagon receptor agonist, building on the incretin biology established by earlier GLP-1 and dual GIP/GLP-1 agonists. Coskun and colleagues published its discovery and pharmacology, and it subsequently advanced through clinical evaluation as an investigational metabolic agent.

References
  1. Coskun T, et al. (2022). LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: from discovery to clinical proof of concept. Cell Metabolism.
  2. Jastreboff AM, et al. (2023). Triple-Hormone-Receptor Agonist Retatrutide for Obesity - A Phase 2 Trial. New England Journal of Medicine.
  3. Rosenstock J, et al. (2023). Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes: a randomised, double-blind, placebo- and active-controlled, parallel-group, phase 2 trial. The Lancet.

View compound profile on NIH PubChem →

Cited literature refers to laboratory and preclinical research. GLP-3 (Retatrutide) is supplied strictly for research use only and is not intended to diagnose, treat, cure, or prevent any disease.

Why researchers choose Helio
99%+ PurityHPLC-verified every batch
Accredited TestingIndependent ISO 17025 laboratory
Per-Batch COADocumentation tied to your lot
Made in the USADiscreet, protected shipping
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