Tirzepatide
Dual GIP and GLP-1 receptor agonist with the deepest weight-change effect of any approved incretin.
Long-acting GLP-1 receptor agonist — the reference compound for incretin-based metabolic research.
| SKU | Per vial | Pack | |
|---|---|---|---|
| SM5 | 5 mg | 10 vials / box | |
| SM10 | 10 mg | 10 vials / box | |
| SM15 | 15 mg | 10 vials / box | |
| SM20 | 20 mg | 10 vials / box | |
| SM30 | 30 mg | 10 vials / box |
Pricing is quoted directly and is competitive at every tier — message us with the SKUs you want and quantities for a quote.
Replies within 36 hours. Cryptocurrency (preferred) or card / money-app with a processing fee. COA for this batch available on request.
Semaglutide is a 31-amino-acid glucagon-like peptide-1 (GLP-1) analogue engineered with a C18 fatty-diacid side chain that binds albumin, extending its half-life to roughly one week. It activates the GLP-1 receptor, which is expressed in pancreatic islets, the gastrointestinal tract and hypothalamic appetite circuits.
In the 68-week STEP 1 trial (n = 1,961), once-weekly semaglutide 2.4 mg produced a mean body-weight change of −14.9% versus −2.4% with placebo in adults with overweight or obesity 1. It is among the most extensively characterised peptides in the metabolic literature and serves as the benchmark against which newer incretin compounds are compared.
Sequence, formula and CAS data are provided for identification. Batch-specific purity, mass-spec and HPLC data are on the Certificate of Analysis — ask for it with your order.
Citations retrieved from PubMed (NCBI). Links open the publisher record via DOI and the PubMed abstract.
Dual GIP and GLP-1 receptor agonist with the deepest weight-change effect of any approved incretin.
Triple GIP / GLP-1 / glucagon receptor agonist — the next generation of incretin research.
Co-formulated amylin analogue and GLP-1 agonist in a single vial — the CagriSema research model.