Retatrutide
LY3437943, triple GIP/GLP-1/glucagon receptor agonist
A single-molecule triple agonist at the GIP, GLP-1 and glucagon receptors — the most-discussed metabolic research peptide of the current cycle.
Scan the QR code on your vial, or type the batch number, and you get the analytical data for the exact vial you received.
Verify your vial →LY3298176, dual GIP/GLP-1 receptor agonist
A unimolecular dual agonist of the GIP and GLP-1 receptors, and the compound behind the SURMOUNT and SURPASS trial programmes.
Tirzepatide is a 39-amino-acid synthetic peptide engineered as a single molecule that activates both the GIP and GLP-1 receptors, with a C20 fatty diacid moiety conferring once-weekly pharmacokinetics. The SURMOUNT-1 trial reported substantial and sustained weight reduction over 72 weeks in participants with obesity, and three-year data in participants with obesity and prediabetes reported markedly lower progression to type 2 diabetes versus placebo. Gastrointestinal adverse events were the most common finding and were generally mild-to-moderate and transient.
Price is per single sealed vial, in USD. Buying several — volume pricing.
| Vial strength | Price | |
|---|---|---|
| 2mg | $75.60 | Order 2mg |
| 5mg | $46 | Order 5mg |
| 10mg | $66 | Order 10mg |
| 15mg | $78 | Order 15mg |
| 20mg | $93 | Order 20mg |
| 30mg | $118 | Order 30mg |
| 40mg | $148 | Order 40mg |
| 50mg | $163 | Order 50mg |
| 60mg | $208 | Order 60mg |
| 80mg | $621.60 | Order 80mg |
| 100mg | $705.60 | Order 100mg |
Links open peer-reviewed sources on PubMed. These are provided so you can read the primary literature yourself. Citing a study is not a claim that this compound is safe or effective for any use in humans.
LY3437943, triple GIP/GLP-1/glucagon receptor agonist
A single-molecule triple agonist at the GIP, GLP-1 and glucagon receptors — the most-discussed metabolic research peptide of the current cycle.
TH9507, trans-3-hexenoyl-GHRH(1-44)
A stabilised GHRH(1-44) analog and the only GH-axis compound with regulatory approval specifically for reducing visceral adipose tissue.
A small-molecule NNMT inhibitor studied in adipocyte metabolism and NAD+ salvage research.
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