Semaglutide

In simple terms, semaglutide helps the body: feel full, eat less, control blood sugar.

SKU: BND3-SEMA Category:

Product Details

Parameter Specification
Purity ≥ 99% (HPLC, third-party tested)
Form Lyophilized peptide powder
Content 10 mg Semaglutide per vial
Packaging Glass vial with sterile closure
Storage Conditions Store lyophilized at 2–8 °C (desiccated, protect from light)
Molecular Formula C187H291N45O59
Molecular Weight ~4113.6 g·mol⁻¹
Amino Acid Sequence GLP-1 analog peptide with C18 fatty diacid side chain (modified for prolonged activity)
CAS Number 910463-68-2
Solubility Bacteriostatic water

Overview

Semaglutide is a synthetic analog of glucagon-like peptide-1 (GLP-1) and belongs to the class of GLP-1 receptor agonists (GLP-1RA). It is structurally modified to increase stability and extend its half-life, allowing prolonged biological activity. It represents a major advancement in: metabolic research, weight regulation, glucose control (Drucker, 2018).

What it is and how it works

Semaglutide mimics endogenous GLP-1 and works by: stimulating glucose-dependent insulin secretion, suppressing glucagon release, slowing gastric emptying, acting on appetite centers in the brain (Davies et al., 2017).

Effects confirmed by research

1. Weight loss

  • ~10–15% body weight reduction, reduced appetite, improved eating control (Wilding et al., 2021).

2. Glycemic control

  • lowers blood glucose, improves HbA1c, supports beta-cell function (Marso et al., 2016).

3. Cardiovascular effects

  • reduced cardiovascular risk, improved lipid profile.

4. Appetite regulation (CNS)

  • reduced hunger, increased satiety, altered food reward pathways.

5. Liver and metabolic effects

  • reduced liver fat, improved metabolic markers (Newsome et al., 2021).

Scientific description

Semaglutide is: a long-acting GLP-1 receptor agonist, regulator of: glucose metabolism, appetite signaling, metabolic health.

References

Drucker, D. J. GLP-1 mechanisms. Cell Metabolism. 2018. Davies, M., et al. Semaglutide pharmacology. Lancet Diabetes Endocrinol. 2017. Wilding, J. P. H., et al. STEP trial. NEJM. 2021. Marso, S. P., et al. SUSTAIN-6. NEJM. 2016. van Bloemendaal, L., et al. GLP-1 brain effects. Diabetes. 2014. Newsome, P. N., et al. Semaglutide in NASH. NEJM. 2021.