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For in vitro laboratory research use only/Not for human or veterinary use
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Semaglutide 10mg vial

In stock

Semaglutide

10mg · Single vial · Lyophilized powder

Single vial74.99CAD

Metabolic research

Semaglutide is a long-acting GLP-1 receptor agonist lyophilized compound, commonly used in metabolic and glucose regulation research.

  • Studied in women's metabolic research contexts including PCOS insulin resistance models and postmenopausal glucose regulation
  • Appears in GLP-1 receptor pharmacology literature investigating sex-specific pharmacokinetics
  • Referenced in body composition and appetite signaling research

Order

1
Dose
10mg
Pack size
Single vial
Form
Lyophilized powder
Storage
2–8°C

In vitro laboratory research use only · Not for human or veterinary use · Batch documented · Third-party tested · Ships from Canada

§ Research

Research · Semaglutide

Overview

Semaglutide is a synthetic analog of endogenous GLP-1 with 94% structural homology to the native sequence. It incorporates a C-18 fatty diacid side chain enabling non-covalent albumin binding, extending systemic half-life to approximately 7 days. Widely used as a reference compound in GLP-1 receptor pharmacology research.

Mechanism of action

Activates the GLP-1 receptor, a G-protein-coupled receptor expressed in pancreatic beta cells, the central nervous system, and the gastrointestinal tract. Receptor activation stimulates glucose-dependent insulin secretion, suppresses glucagon release, and delays gastric emptying. The C-18 modification reduces renal clearance and confers resistance to proteolytic degradation.

Key research findings

  1. 01

    Established as a reference agonist in GLP-1 receptor binding and signaling studies across cellular and animal models.

  2. 02

    Preclinical rodent studies characterize dose-dependent effects on glucose tolerance and insulin secretion at pharmacologically relevant exposures.

  3. 03

    Longitudinal cardiovascular outcomes trial data (SELECT, 2023) have characterized the compound's effects on major adverse cardiovascular events in participants with established cardiovascular disease.

  4. 04

    Clinical pharmacokinetic studies document approximately 165-hour half-life, supporting once-weekly administration regimens in investigational use.

Published references

  • Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes

    Lincoff AM et al. — N Engl J Med, 2023 · PMID: 37952131

  • The Discovery and Development of Liraglutide and Semaglutide

    Knudsen LB et al. — Front Endocrinol (Lausanne), 2019 · PMID: 31031702

The information above is derived from published preclinical and clinical research. It is provided for educational purposes only and does not constitute medical advice, diagnosis, or treatment recommendations.

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