
Ozempic / Wegovy Analog
Semaglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist that has demonstrated significant efficacy in metabolic research. It works by mimicking the GLP-1 hormone, which stimulates insulin secretion and reduces glucagon secretion in a glucose-dependent manner. Our pharmaceutical-grade semaglutide is produced via solid-phase peptide synthesis (SPPS) with rigorous quality control at every stage.
B2B Wholesale Only · For Research Use Only · COA Provided with Every Order
Semaglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist that has demonstrated significant efficacy in metabolic research. It works by mimicking the GLP-1 hormone, which stimulates insulin secretion and reduces glucagon secretion in a glucose-dependent manner. Our pharmaceutical-grade semaglutide is produced via solid-phase peptide synthesis (SPPS) with rigorous quality control at every stage.
His-Aib-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Lys-Glu-Phe-Ile-Ala-Trp-Leu-Val-Arg-Gly-Arg-NH₂
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Peer-reviewed scientific literature on Semaglutide from PubMed, NEJM, The Lancet, and other authoritative sources.
Research Use Only. The following citations are provided for informational purposes and represent independent scientific research. These studies do not constitute medical advice or claims about our products. All products are sold for research purposes only and are not intended for human use.
Wilding JPH, Batterham RL, Calanna S, et al.
New England Journal of Medicine, 384: 989–1002 (2021)
Participants receiving semaglutide lost a mean of 14.9% of body weight vs. 2.4% with placebo (p<0.001). 86.4% of semaglutide participants achieved ≥5% weight loss.
Lincoff AM, Brown-Frandsen K, Colhoun HM, et al.
New England Journal of Medicine, 389: 2221–2232 (2023)
Semaglutide reduced the risk of major adverse cardiovascular events by 20% (HR 0.80; 95% CI 0.72–0.90; p<0.001) compared to placebo over a mean follow-up of 39.8 months.
Ryan DH, Lingvay I, Colhoun HM, et al.
Obesity, 28: 1050–1061 (2020)
The STEP program demonstrated consistent and clinically meaningful weight reductions with semaglutide 2.4 mg across diverse patient populations, establishing a new benchmark for pharmacological obesity treatment.
Citations sourced from PubMed / NCBI, New England Journal of Medicine, The Lancet, Nature, and other peer-reviewed publications. DOI links lead to original publisher pages.

Dual GIP/GLP-1 receptor agonist. Widely used in metabolic and weight management research.

Triple-agonist candidate for advanced metabolic regulation and adiposity research.

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