Products › Retatrutide
Longevity/Metabolic

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

A synthetic triple agonist peptide targeting the GIP, GLP-1, and glucagon receptors, studied in preclinical and clinical metabolic research.

CAS Number
2381089-83-2
Sequence
39-amino-acid modified peptide, acylated for albumin binding (proprietary analog sequence)
Molecular Formula
C223H347N47O68
Molecular Weight
4731.4 g/mol
Purity
≥98% (HPLC)
Form
Lyophilized powder
Vial Content
20mg per vial
Documentation
COA & HPLC Analysis
See our quality assurance & testing process ›

Overview

Retatrutide is a synthetic, fatty-acid-acylated peptide engineered to act as a combined agonist at glucose-dependent insulinotropic polypeptide (GIP), glucagon-like peptide-1 (GLP-1), and glucagon receptors. It represents a research extension of the dual and single incretin-receptor agonist compounds that preceded it, and has been studied in both preclinical models and published clinical trial research on metabolic regulation. Peptide Factory supplies Retatrutide as a lyophilized powder for laboratory research.

Research Background

Acylation of the peptide backbone with a fatty-acid moiety promotes reversible albumin binding, extending its research half-life relative to native incretin hormones. Receptor-binding assays have characterized Retatrutide’s balanced activity across all three target receptors, and this triple-agonism has become a central research question in comparative incretin pharmacology: how simultaneous GIP, GLP-1, and glucagon receptor engagement affects energy expenditure and substrate metabolism relative to single- or dual-agonist compounds.

Studied Applications

Preclinical and clinical research on Retatrutide has examined:

  • Energy expenditure and substrate metabolism research — animal and human research studies have investigated the combined receptor agonism’s effect on resting energy expenditure, lipid oxidation, and glucose disposal.
  • Body composition research — published clinical trial data has examined changes in body weight and composition markers in research cohorts, motivating comparative interest against single- and dual-agonist incretin compounds.
  • Glycemic control research — receptor-binding and functional studies have investigated Retatrutide’s effect on insulin secretion and glucagon counter-regulation in metabolic research models.

Peptide Factory’s Retatrutide is supplied strictly for laboratory research and analytical use — it is an investigational compound, not an approved therapeutic, and no dosing or administration guidance is provided.

Storage & Handling

Store lyophilized Retatrutide at -20°C, protected from light and moisture. See our storage and handling guidance for reconstitution protocols.

References

  • Jastreboff, A. M. et al. “Triple-hormone-receptor agonist retatrutide for obesity — a phase 2 trial.” N. Engl. J. Med. research literature.
  • Coskun, T. et al. Retatrutide receptor pharmacology and preclinical metabolic research.
  • Rosenstock, J. et al. GIP/GLP-1/glucagon triple agonism research review.

For Research Use Only — Not for Human Consumption.

Frequently Asked

What makes Retatrutide a 'triple agonist'?
Retatrutide is engineered to activate three distinct incretin/glucagon-family receptors — GIP, GLP-1, and glucagon receptors — simultaneously, distinguishing it from single- or dual-receptor incretin research compounds.
Is Retatrutide approved for human use?
No. As of this writing, Retatrutide remains an investigational compound studied in clinical trials for metabolic research. Peptide Factory supplies it exclusively as a research-grade compound for laboratory and analytical use.

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For Research Use Only — Not for Human Consumption