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≥99% PurityGLP-1 S vialUSA Lab VerifiedISO/IEC 17025

GLP-1 S

GLP-1 Receptor Studies

$85.00$42.50/vial with BOGO
USA Lab VerifiedISO/IEC 17025:2017View COA
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Your results are only as good as your compound. Every lot of GLP-1 S is tested by an independent ISO/IEC 17025-accredited lab in the USA. 99%+ purity isn't a target here. It's the requirement. Don't take our word for it: test any vial at an accredited lab of your choice. If HPLC purity comes back under 99%, we refund your order and pay for the test.

Size
20mg
Purity
99%+ by HPLC · guaranteed
Identity
Confirmed by mass spec
Lab
Accurate Test Labs · ISO/IEC 17025
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About this compound

GLP-1 S is a selective GLP-1 receptor agonist peptide. Its sequence is about 94 percent identical to the endogenous GLP-1 hormone, with one change that resists enzymatic cleavage. Research has measured insulin release, appetite signalling and gastric emptying. A fatty acid chain lets it bind albumin, which extends its half-life.

GLP-1 receptor agonist (incretin mimetic)

Formula
C187H291N45O59
Molecular weight
4113.58 g/mol
Form
Lyophilized powder
CAS / ID
910463-68-2
Read the full GLP-1 S research monograph
Research Snapshot

GLP-1 S research, by the numbers.

The numbers that define GLP-1 S and how it is being studied. For laboratory research use only.

  • 94%

    Sequence Identity to GLP-1

    Two substitutions vs native human GLP-1

  • 0.38 nM

    GLP-1R Binding Affinity

    Measured affinity at the GLP-1 receptor

  • 165h

    Plasma Half-Life

    Extended plasma half-life

  • 4

    Research Areas

    • Incretin Receptor Signaling
    • Glycemic Pathways
    • Cardiometabolic Research
How It Works

How GLP-1 S works

The pathways GLP-1 S acts on - and what each one does. The animation traces its signal outward from the compound to every target it engages.

Signalling pathways studied in preclinical models · illustrative
GLP-1 Receptor Agonism
GLP-1R

Selectively binds GLP-1 receptors. Published characterisation describes glucose-dependent insulin secretion, glucagon suppression and delayed gastric emptying in study models. Insulin response scales with glucose, a property examined relative to non-incretin secretagogues.

  • Glucose-dependent insulin secretion
  • Glucagon suppression
  • Delayed gastric emptying
Central GLP-1R Signalling
CNS

Engages GLP-1 receptors in the hypothalamus and hindbrain, with hunger, satiety and energy intake as the measured endpoints.

  • Food intake measured
  • Satiety signalling measured
  • Lower caloric intake
Extended Half-Life Design
PK

A C18 fatty-diacid chain confers reversible albumin binding and resistance to DPP-4 degradation, extending the plasma half-life to roughly 7 days in research models.

  • ~165-hour half-life
  • Albumin-binding modification
  • DPP-4 resistant
Uses & Applications

What GLP-1 S is researched for

The main areas GLP-1 S is being studied for - and the study-reported figures behind them.

Metabolic

Metabolic Receptor Research

GLP-1 receptor agonism is a principal focus of metabolic research, and GLP-1 S is a selective agonist used as a reference compound in that work.

Endocrine

Glycemic Pathway Research

GLP-1 S is studied for glucose-dependent insulin secretion and glycemic endpoints in metabolic research.

Cardiometabolic

Cardiovascular Outcomes

Cardiometabolic signalling is a further area of research interest for this receptor class, beyond glucose handling.

Neuroscience

Hypothalamic & Reward Circuitry

GLP-1 receptor signaling in the hypothalamus and hindbrain modulates satiety and food-reward pathways, a focus of ongoing neuroscience research.

Study-reported magnitudes

Representative figures from published research. Bars fill as you scroll.

HPLC Purity (lot COA)≥99%
Sterility & Endotoxin ScreenPASSED
Net Content & IdentityPASSED

Figures are representative of published research findings and shown for reference.

Molecular Structure

The GLP-1 S molecule

An interactive 3D model rendered from the compound record - rotate and explore its structure.

C187H291N45O59

Molecular formula
C187H291N45O59
Molecular weight
4113.58 g/mol
Sequence length
31 residues
CAS / ID
910463-68-2
Physical form
Lyophilized powder
Documented purity
≥99% by HPLC
How Long It Lasts

Duration & clearance

How GLP-1 S clears from circulation, modeled from its documented ~~165 hours (~7 days) half-life. The curve draws as you scroll.

GLP-1 S · ~~165 hours (~7 days)
Reference · rapid clearance
Compound Information

Full specification

Compound ClassGLP-1 receptor agonist (incretin mimetic)
Research NameGLP-1 S
TargetGLP-1 receptor (GLP-1R)
FormLyophilized powder
Molecular Weight4,113.58 g/mol
Purity≥99% (HPLC verified)
TestingThird-party HPLC, Mass Spec, Endotoxin
Half-Life~165 hours (~7 days)
Storage-20°C for long-term stability
SolubilityWater-soluble
COAIncluded with every order
FAQ

Common questions about GLP-1 S

GLP-1 S is a long-acting and selective GLP-1 receptor agonist. It mimics the incretin hormone GLP-1; published characterisation describes glucose-dependent insulin secretion, glucagon suppression, delayed gastric emptying and central appetite-pathway signalling.

GLP-1 S is a single-receptor (GLP-1) agonist. GLP-2 TZ is a dual GLP-1/GIP agonist, and GLP-3 RT is a triple GLP-1/GIP/glucagon agonist. The distinction is receptor coverage.

GLP-1 S has a molecular weight of 4,113.58 g/mol. Every vial is supplied at ≥99% purity, verified by HPLC, with a Certificate of Analysis included.

Store lyophilized vials at -20°C for long-term stability, protected from light and moisture.

No. GLP-1 S is sold strictly as a research compound for laboratory and in-vitro use only. It is not intended for human or animal consumption, diagnosis, or treatment.

Research Use Only.

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