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.
Every box carries a batch number. Look it up and you get the analytical data for the exact vials you received.
Batch lookup →Mitochondrial ORF of the 12S rRNA type-c
A 16-amino-acid peptide encoded in mitochondrial DNA rather than the nuclear genome — a mitochondrial-derived peptide studied as an exercise mimetic.
MOTS-c is translated from a short open reading frame within the mitochondrial 12S rRNA gene, making it one of a small class of mitochondrially encoded hormones. Published work reports that it targets skeletal muscle, regulates the folate–methionine cycle, activates AMPK, and improves insulin sensitivity in rodent models of diet-induced obesity. It is described in the literature as exercise-induced, with treatment of aged mice reported to improve physical capacity and produce adaptations resembling those of physical activity. A pro-diabetogenic mtDNA polymorphism within MOTS-c has been characterised in East Asian populations.
Prices in USD per sealed box of 10 vials. Bulk pricing available from 10 boxes — see wholesale.
| Vial strength | Box | Price | |
|---|---|---|---|
| 10mg | 10 vials |
$151.20
$15.12 per vial
|
Order 10mg |
| 40mg | 10 vials |
$532
$53.20 per vial
|
Order 40mg |
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.
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.
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