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 →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.
Retatrutide activates three receptors from one molecule: GLP-1, GIP and glucagon. The glucagon arm is what distinguishes it from dual agonists — it is proposed to add an energy-expenditure component on top of the appetite and gastric-emptying effects of GLP-1/GIP agonism. A 48-week phase 2 obesity study reported mean weight reductions of 22.8% and 24.2% at the 8 mg and 12 mg doses. Separate phase 2a work reported reductions in liver fat content in metabolic dysfunction-associated steatotic liver disease. Gastrointestinal events were the most frequently reported adverse effects across trials.
Price is per single sealed vial, in USD. Buying several — volume pricing.
| Vial strength | Price | |
|---|---|---|
| 5mg | $75 | Order 5mg |
| 10mg | $118 | Order 10mg |
| 15mg | $153 | Order 15mg |
| 20mg | $168 | Order 20mg |
| 30mg | $208 | Order 30mg |
| 50mg | $333 | Order 50mg |
| 60mg | $338 | Order 60mg |
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.
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.
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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