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GLRT3 10mg

GLRT3 10mg

Regular price $110.00
Sale price $110.00 Regular price $150.00
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GLRT3 10mg

Regular price $110.00
Sale price $110.00 Regular price $150.00
SAVE 26% Sold out

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Each vial contains 10mg or 20mg of highly pure Retatrutide.

Retatrutide is classified as a triple glucagon hormone receptor agonist (GLP-1, GIP, and GCGR receptors), making it more effective for body fat mass reduction than its predecessor Semaglutide by targeting further receptors.

Add 1mL of bacteriostatic water to get a solution that is 10mg/mL, such that every 0.1mL (10 units on an insulin syringe) is equal to 1mg of Retatrutide.
This product must be refrigerated after reconstitution.
View full details

01The PureChain Standard

Purity And Documentation

Your results are only as good as the compound you start with.

Every vial is labelled with its compound, vial size and molecular weight, and ships for laboratory research use only. Third-party testing details will be published here.

Supplied for in-vitro laboratory research only. Not for human or veterinary use, and not intended to diagnose, treat, cure or prevent any disease.

Size
10mg
Form
Lyophilized powder
Storage
−20 °C, protected from light
Molar mass
4731.3 Da

About This Compound

About Retatrutide

Retatrutide is a synthetic peptide agonist that engages three receptors at once: the glucose-dependent insulinotropic polypeptide receptor, the glucagon-like peptide-1 receptor and the glucagon receptor. That is the whole design idea. Single-agonist compounds act on GLP-1R alone and dual agonists add GIPR; retatrutide adds the glucagon receptor as a third arm, which brings energy expenditure into the same molecule as the incretin effects. It is a research compound with no public PubChem structural record, so the formula and molecular mass below are taken from concurring published supplier data and cited under the structure.

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

Molecular Formula

C221H342N46O68

Molecular Weight

4731.3 g/mol

Form

Lyophilized Powder

CAS Number

2381089-83-2

02Molecular Structure

The Retatrutide molecule

An illustrative atomic representation generated from the compound record, alongside its verified molecular data. The structure figure is schematic – not a measured conformation.

  • C
  • H
  • N
  • O
  • S/P
Molecular Formula C221H342N46O68
Molecular Weight 4731.3 g/mol
Chemical Name Retatrutide (LY3437943)
Physical Form Lyophilized Powder
CAS Number 2381089-83-2
Use Class Research use only

No PubChem structural record exists for this compound. Molecular data from Selleck Chemicals and Cayman Chemical product data. View the source

By The Numbers

Retatrutide Research, By The Numbers

The figures that define Retatrutide and how it is being studied. For laboratory research use only.

3

Receptor Targets

GIP, GLP-1 and glucagon receptors engaged by one molecule

GIPR

First Arm

The glucose-dependent insulinotropic polypeptide receptor

GCGR

The Distinguishing Arm

The glucagon receptor, which dual agonists do not engage

4

Research Areas

  • Incretin Receptor Pharmacology
  • Metabolic Research
  • Multi-Agonist Design
  • Energy Expenditure Models

How It Works

How Retatrutide Works

The pathways Retatrutide acts on, and what each one does. Described from preclinical and receptor-pharmacology literature.

GLP-1R Agonism

The Established Incretin Arm

The glucagon-like peptide-1 receptor is the best-characterised incretin target, studied for glucose-dependent insulin secretion and for signalling in the central nervous system. It is the arm retatrutide shares with every other compound in this class.

  • Glucose-dependent insulin secretion in islet models
  • Central nervous system receptor expression
  • The common arm across all incretin agonists
GIPR Agonism

The Second Incretin Receptor

GIP is the other incretin hormone, and adding its receptor is what separates dual agonists from single ones. Research on combined GIPR and GLP-1R engagement examines whether the two pathways act additively or through distinct mechanisms.

  • The second incretin pathway alongside GLP-1
  • Distinguishes dual agonists from single agonists
  • Studied for additive versus distinct signalling
GCGR Agonism

The Third Arm, And The Design Trade-Off

Glucagon receptor agonism is the arm unique to triple agonists. It is associated with energy expenditure and hepatic metabolism, and balancing it against the incretin arms is the central question in multi-agonist peptide design.

  • The arm unique to the triple-agonist class
  • Associated with energy expenditure and hepatic pathways
  • Ratio balancing is the core design problem

Signalling pathways studied in preclinical models. Illustrative, not a claim of effect in humans.

Uses And Applications

What Retatrutide Is Researched For

The main areas Retatrutide is studied in, and the qualitative magnitudes reported alongside them.

Incretin Receptor Pharmacology

Used to study how a single molecule engaging three receptors compares against separate agonists for each.

Metabolic Research

Applied in preclinical metabolic models examining glucose handling, insulin secretion and energy balance.

Multi-Agonist Peptide Design

A reference compound for the design question of how to balance potency ratios across several receptors in one sequence.

Energy Expenditure Models

The glucagon receptor arm makes retatrutide the tool of choice where energy expenditure, not just incretin signalling, is the variable under study.

Study-Reported Magnitudes

Qualitative summaries of published research. Bars fill as you scroll.

Number Of Receptor Targets Three
GLP-1 Receptor Arm Present
GIP Receptor Arm Present
Glucagon Receptor Arm Present

Figures are representative summaries of published research findings, shown for reference only. They are not claims about outcomes in humans.

Compound Information

Full Specification

Chemical Name Retatrutide (LY3437943)
Molecular Weight 4731.3 Da
Molecular Formula C221H342N46O68
CAS Number 2381089-83-2
Form Lyophilized powder
Solubility Water-soluble
Storage Store lyophilized at −20 °C, protected from light and moisture
Vial Size 10mg
Structural Record No PubChem entry; values from published reference data

FAQ

Common Questions About Retatrutide

What Is Retatrutide?

A synthetic peptide agonist at three receptors – GIP, GLP-1 and glucagon – also referred to as LY3437943. It is supplied here as a research compound.

Where Do The Molecular Figures On This Page Come From?

Retatrutide has no public PubChem structural record. The formula and molecular mass shown are taken from published supplier reference data, and the source is cited directly under the structure. Every other compound in this catalogue is sourced from PubChem and cites its CID.

How Does A Triple Agonist Differ From A Dual Agonist?

By the third receptor. Dual agonists engage GIP and GLP-1 receptors; a triple agonist adds the glucagon receptor, which brings energy expenditure pathways into the same molecule.

What Are Incretins?

Gut hormones released in response to food that stimulate insulin secretion in a glucose-dependent way. GLP-1 and GIP are the two principal incretins in humans.

Is Retatrutide Approved For Human Use?

No. It is supplied as a research chemical for in-vitro laboratory work only, and is not supplied for human or veterinary use.

How Should Research-Grade Retatrutide Be Stored?

Store the lyophilized powder at −20 °C, protected from light and moisture, and refrigerate after reconstitution. Aliquot to avoid repeated freeze-thaw cycles.

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Research Use Only

Not for human or veterinary use. For in-vitro laboratory research only. These statements have not been evaluated by the FDA or Health Canada; this product is not intended to diagnose, treat, cure or prevent any disease.