GLP-1 5mg

$150.00

≥99% purity · HPLC verified · MS confirmed How we test → Download COA
Products will arrive in a lyophilized (powder) form for maximum stability
Semaglutide is a long-acting GLP-1 receptor agonist and the most extensively studied peptide in its class, with research spanning diabetes, obesity, cardiovascular, and kidney models. Its DPP-4-resistant design supports a ~7-day half-life and once-weekly dosing in preclinical protocols. The 5mg vial format suits shorter studies, supplied at ≥99% HPLC purity, for research use only.

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Compound Identity

COMPOUND NAME

Semaglutide

SYNONYMS

NN9535

CAS NUMBER

910463-68-2

MOLECULAR FORMULA

C187H291N45O59

MOLECULAR WEIGHT

~4113.58 g/mol

STRUCTURE

Peptide sequence with modifications to enhance stability; includes Aib at position 8, Arg at position 34, and a C18 fatty diacid moiety attached to lysine 26 via a hydrophilic spacer.

PEPTIDE SEQUENCE

H-Aib-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gln-Lys-Ala-Ala-Gln-Ala-Ala-Lys-Glu-Phe-Ile-Ala-Trp-Leu-Val-Arg-Gly-Arg-NH?

CHEMICAL STRUCTURE

Semaglutide peptide molecular formula diagram

Source: PubChem

Mechanism of Action

Semaglutide is a potent, selective GLP-1 receptor agonist. It stimulates the GLP-1 receptor in pancreatic ?-cells to enhance glucose-dependent insulin secretion, suppresses pancreatic ?-cell glucagon secretion, and directly acts on appetite-regulating centers in the brain. The result is pronounced postprandial and fasting blood glucose reduction, delayed gastric emptying (transient), reduced hunger, enhanced satiety, and decreased caloric intake. Structural modifications protect against DPP-4 degradation and extend the peptide’s half-life, allowing once-weekly dosing

1

Pancreas: Enhanced glucose-dependent insulin secretion; glucagon suppression, lowering hepatic glucose output

2

Central Nervous System: Decreases food intake by targeting homeostatic and hedonic appetite pathways (hindbrain/hypothalamus), reducing hunger and cravings, and enhancing satiety

3

Gastrointestinal Tract: Delays gastric emptying, contributing to satiety (transient effect at higher doses)

4

Adiposity/Energy Intake: Weight loss is primarily driven by sustained reduction in caloric intake, not increased energy expenditure

Biological Activity

Potent GLP-1 receptor agonist Enhances insulin secretion (glucose-dependent) Suppresses glucagon secretion Reduces appetite and caloric intake Produces significant, sustained body weight loss Improves cardiometabolic risk factors (glycemia, blood pressure, lipids)

Storage

  • Refrigerate once reconstituted. Protect from light and moisture.

Drug Categories

Amino Acids, Peptides, and Proteins; Lipids

Additional Notes

  • Engineered for DPP-IV resistance and long half-life via fatty-acid conjugation
  • Demonstrates the highest anti-obesity efficacy of any currently approved agent

Summary Table

Property
Description
CAS Number
910463-68-2
Molecular Formula
C187H291N45O5
Molecular Weight (MW)
~4113.58 g/mol
Mechanism of Action
GLP-1 receptor agonist; enhances insulin, suppresses glucagon, reduces appetite and energy intake
Biological Activity
Antidiabetic, anti-obesity; improves glycemic control, reduces weight and cardiometabolic risk factors
Supplied Form
Lyophilized powder (research use); solution for injection (clinical)
Purity
≥95% (HPLC)
Storage
-20°C to -80°C, dry, protected from light
Drug Categories
Amino Acids, Peptides, and Proteins; Lipids
Additional Notes
Modifications provide extended half-life for clinical formulation

Disclaimer

For Research Use Only. Not intended for human or veterinary use. This compound is supplied solely for laboratory and R&D purposes.

Detailed Product Description

Semaglutide is a modified GLP-1 analog containing 94% sequence homology with native human GLP-1. Key structural changes—Aib substitution at position 8, Arg at position 34, and C18 fatty diacid conjugation at Lys26—enable reversible albumin binding and confer resistance to DPP-4-mediated degradation. This results in a long half-life (approximately 7 days), making it suitable for once-weekly subcutaneous injection. Semaglutide robustly reduces appetite, promotes satiety, and significantly decreases body weight and glycemic parameters in both obese/overweight individuals and those with type 2 diabetes.

Research Highlights

Sustained Weight Loss: Reductions of 8–16%+ of baseline body weight over 1–2 years; 86% of patients lose at least 5% of baseline weight; up to 32% lose ?

20%

Glycemic Control: HbA1c reductions up to 1.

9% vs placebo, with effects on both fasting and postprandial glucose

Cardiometabolic Improvement: Decreases in blood pressure, waist circumference, lipid fractions, and inflammatory biomarkers; improved quality of life metrics

Head-to-Head Studies: Outperforms once-daily liraglutide 3.

0 mg, orlistat, phentermine–topiramate, and naltrexone–bupropion for weight loss efficacy

Pharmacokinetic Profile

Route of Administration

SC

Dosing Frequency

Once weekly

Half-Life

184 hours

  • Route of Administration: Subcutaneous
  • Dosing Frequency: Once weekly (subcutaneous)
  • Half-Life: ~155–184 hours (6.5–7.7 days), supporting once-weekly SC dosing
  • Formulation:

Formulation & Handling

  • Reconstitute in sterile water or PBS (pH ~7.4) for in vivo/in vitro use
  • Store at –20°C in aliquots to prevent freeze-thaw degradation
  • Shelf-stable for 12 months under recommended storage condition

Clinical Trial Activity

Trial ID
Title
Phase
Study Type
Sponsor
NCT0354893
STEP 1: Once-Weekly Semaglutide in Adults with Overweight or Obesity
3
Intervention
NN
NCT0355275
STEP 2: Semaglutide in Adults with Overweight/Obesity and Type 2 Diabetes
3
Intervention
NN
NCT0361158
STEP 3: Semaglutide plus Intensive Behavioral Therapy in Obesity
3
Intervention
NN
NCT0354898
STEP 4: Weight Loss Maintenance with Semaglutide
3
Intervention
NN
NCT04573528
SELECT: Semaglutide Effects on Heart Disease and Stroke in Obesity
3
Intervention
NN

References

1
Wilding, J. P. H. et al. Once-weekly semaglutide in adults with overweight or obesity. N. Engl. J. Med. 384, 989–1002 (2021). https://doi.org/10.1056/NEJMoa2032183
2
Davies, M. et al. Effect of oral semaglutide compared with placebo and subcutaneous semaglutide on glycemic control in patients with type 2 diabetes: a randomized clinical trial. JAMA 318, 1460–1470 (2017). https://doi.org/10.1001/jama.2017.14752
3
Lau, D. C. W., Batterham, R. L. & le Roux, C. W. Pharmacological profile of once-weekly injectable semaglutide for chronic weight management. Expert Rev. Clin. Pharmacol. 15, 251–268 (2022). https://doi.org/10.1080/17512433.2022.2070473
4
Rubino, D. et al. Effect of continued weekly subcutaneous semaglutide vs placebo on weight loss maintenance in adults with overweight or obesity: the STEP 4 randomized clinical trial. JAMA 325, 1414–1425 (2021). https://doi.org/10.1001/jama.2021.3224
5
Lambers Heerspink, H. J. et al. Semaglutide in patients with overweight or obesity and chronic kidney disease without diabetes: a randomized double-blind placebo-controlled clinical trial. Nat. Med. 31, 278–285 (2025). https://doi.org/10.1038/s41591-024-03327-6
6
This product is synthesized via solid-phase peptide synthesis (SPPS) and tested to ≥99% purity by HPLC with identity confirmed by mass spectrometry. A Certificate of Analysis (COA) is available for every batch. Learn about our full quality and testing process →

Quality & Purity

This product is synthesized via solid-phase peptide synthesis (SPPS) and tested to ≥99% purity by HPLC with identity confirmed by mass spectrometry. A Certificate of Analysis (COA) is available for every batch. Learn about our full quality and testing process →

Tested for purity. Verified for identity. Every batch is analyzed by HPLC for ≥99% purity and confirmed by mass spectrometry. Learn about our quality process →