Retatrutide

Overview

Research-use triple incretin and glucagon receptor agonist supplied for studies of integrated metabolic signaling and energy-balance pathway models.

Concentration
10 mg / 20 mg / 40 mg
Stock
Out of stock

Product details

Retatrutide is a synthetic peptide designed for GLP-1, GIP, and glucagon receptor research models of integrated metabolic signaling. Pattern lists this material for controlled laboratory research.

Research Targets: GLP-1 receptor, GIP receptor, glucagon receptor, downstream metabolic signaling networks.

Key Feature: Triple receptor agonist research peptide for multi-hormone pathway studies.

Research Focus Areas: Incretin and glucagon signaling, glucose-regulation pathway models, energy-expenditure models, hepatic metabolic signaling.

Common Models: Receptor assays, rodent metabolic models, liver and adipose signaling systems.

Mechanistic Interests: Multi-receptor activation, insulin and glucagon signaling markers, cAMP pathway dynamics, energy-balance pathway crosstalk.

Use Boundary: Research use only; not for human or veterinary use; no diagnostic, therapeutic, or consumption use is implied.

Product documentation

Certificate of Analysis

Retatrutide

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Research context

Peptide guide

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Guide profile
Triple GIP/GLP-1/Glucagon Agonist
Composition
Investigational synthetic peptide and first-in-class triple agonist targeting glucose-dependent insulinotropic polypeptide (GIP), glucagon-like peptide-1 (GLP-1), and glucagon receptors simultaneously
Discovery
Developed by Eli Lilly as LY3437943, extending dual incretin-agonist research by adding glucagon receptor activation to test broader metabolic effects
Research scope
Phase 2 trials reported large weight reductions and metabolic-marker changes, while confirmatory Phase 3 evidence is still needed for approved-use framing
Regulatory status
Not FDA-approved; investigational pending Phase 3 publication and regulatory review

Safety context

  • Personal or family history of medullary thyroid carcinoma (MTC)
  • Multiple Endocrine Neoplasia syndrome type 2 (MEN2)
  • Hypersensitivity to retatrutide or components

Research-use notice: Retatrutide is an investigational triple-agonist peptide with Phase 2 evidence showing large weight reductions and metabolic effects. It is not FDA-approved as of May 2026, and peer-reviewed Phase 3 efficacy publications, long-term safety data, and cardiovascular outcomes evidence remain pending. Compounded or research-market products lack approved-drug oversight and may vary in quality. Retatrutide's glucagon component introduces unique considerations such as heart-rate changes, so clinical decisions require qualified medical oversight and individualized risk review.

Full guide includes 10 reference entries.

Retatrutide 10 mg
Concentration
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