RESEARCH USE ONLY - Not for human or veterinary use. Supplied for lawful in vitro research and qualified laboratory investigation only. QUALITY - Peptide catalogue items are specified at ≥99% purity with batch documentation. Store lyophilised powders as directed before reconstitution. COMPLIANCE - You are responsible for lawful purchase, possession, and use in your jurisdiction, including institutional and safety requirements. SAFE HANDLING - Use trained personnel, appropriate PPE, and aseptic technique. Do not ingest, inject, or use outside a controlled research setting. POLICIES & ORDERS - Shipping, returns, and research-use terms apply to every order. Read our Research Use Policy and footer legal links before buying.
GLP-RT 5mg lyophilised vial - for research purposes only
GLP-RT 30mg lyophilised vial - for research purposes only
Purity
≥99%
Format
Lyophilised
Documentation
CoA on request
Storage
−20°C
Triple Agonist · Metabolic

GLP-RT — Retatrutide (Triple Agonist)

GLP-1 / GIP / Glucagon receptor agonist

≥99% Purity
CoA Available

GLP-RT is a triple incretin receptor agonist engineered to activate GLP-1, GIP, and glucagon receptors simultaneously. This profile offers a broad metabolic tool for investigation, with published data describing substantial effects on body weight and cardiometabolic markers relative to mono- or dual-agonist comparators.

Size - 5mg
5mg £39.99
30mg £99.99
£39.99
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What is GLP-RT?

GLP-RT is a synthetic 39-amino acid peptide that acts as a unimolecular tri-agonist at receptors for glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP), and glucagon (GCG). This triple mechanism differentiates it from earlier incretin-based compounds.

GLP-1 receptor activation enhances insulin secretion and reduces glucagon output in a glucose-dependent manner, while also promoting satiety and slowing gastric emptying. GIP receptor co-activation potentiates insulin release and has additive effects on body weight reduction. Simultaneous glucagon receptor agonism increases energy expenditure through hepatic and adipose pathways - a mechanism that distinguishes GLP-RT from dual agonists such as GLP-TZ.

The convergence of these three pathways in a single molecule creates a synergistic profile with potential implications for research into obesity, non-alcoholic fatty liver disease (NAFLD/NASH), dyslipidaemia, and type 2 diabetes mellitus.

Product Code
GLP-RT
Receptor Targets
GLP-1R, GIPR, GCGR
Mechanism
Triple Agonist
Molecular Weight
~4,540 Da
Sequence Length
39 Amino Acids

Research Background

Phase 2–style trial data in the literature report remarkable findings for this mechanism class:

  • Mean body weight reductions of up to 24% over 48 weeks at maximum studied doses - exceeding many dual-agonist and monoagonist comparators in published analyses.
  • Statistically significant improvements in HbA1c, fasting glucose, and insulin sensitivity markers.
  • Reductions in triglycerides, LDL-cholesterol, and hepatic fat fraction in participants with metabolic-associated steatotic liver disease.
  • Consistent improvements in waist circumference and visceral adiposity metrics, suggesting meaningful changes in body composition beyond simple weight loss.
  • The glucagon receptor component is hypothesised to drive the incremental efficacy beyond dual agonism through enhanced hepatic glucose output regulation and brown adipose tissue thermogenesis.

Research Applications

GLP-RT is being actively investigated for applications including:

  • Obesity and adiposity research models
  • Type 2 diabetes and insulin resistance mechanistic studies
  • Non-alcoholic fatty liver disease (NAFLD / NASH) investigation
  • Dyslipidaemia and cardiovascular risk marker research
  • Energy expenditure and thermogenesis mechanistic research

Technical Specifications

Appearance
White Lyophilised Powder
Purity
≥99%
Format
Lyophilised (Freeze-Dried)
Reconstitution
Bacteriostatic Water
Storage (Lyophilised)
−20°C, protected from light
Storage (Reconstituted)
2–8°C, use within 28 days
Shelf Life
24 months (lyophilised)
CoA
Available on Request

Frequently Asked Questions

How does GLP-RT differ from GLP-TZ?

Both GLP-RT and GLP-TZ activate GLP-1 and GIP receptors. GLP-RT additionally activates the glucagon receptor, creating a tri-agonist profile. Published data suggest this extra pathway contributes to greater body weight and metabolic effects in some study models versus dual agonism alone.

What reconstitution solvent is recommended?

Bacteriostatic water (0.9% benzyl alcohol) is the standard reconstitution solvent for research use, providing antimicrobial preservation for multi-use vials. Sterile water for injection may also be used for single-use applications.

Is a Certificate of Analysis available?

Yes. A Certificate of Analysis (CoA) documenting batch purity and specifications is available for every batch. Please contact us with your order number to request the relevant documentation.

What are the storage requirements?

Lyophilised GLP-RT should be stored at −20°C, protected from light and moisture. Once reconstituted, store at 2–8°C and use within 28 days. Avoid repeated freeze-thaw cycles of reconstituted product.