
RETA ยท 40 mg / vial
$350
Low stockTriple-agonist research peptide targeting GLP-1, GIP and glucagon receptors.
Retatrutide is a next-generation triple agonist that simultaneously activates the GLP-1, GIP and glucagon receptors โ the three incretin and energy-balance pathways most central to how the body regulates appetite, insulin and fat storage. In clinical research it has produced some of the largest weight reductions ever recorded for a peptide therapeutic, alongside meaningful improvements in glycaemic control, liver fat and cardiometabolic markers.
Think of it as flipping three switches at once. Switch one tells your brain you're full, so you eat less. Switch two helps your body use sugar properly, so less of it gets stored as fat. Switch three turns up your body's own furnace, so you burn more energy all day โ even the stubborn belly and liver fat.
Recommended: use a single-use, sterile drawing syringe and needle for reconstitution โ available in the accessories section.
For in-vitro research only โ not for human or veterinary consumption.
Deep dive ยท properties
Common questions
Semaglutide is a single agonist (GLP-1). Tirzepatide is a dual agonist (GLP-1 + GIP). Retatrutide adds a third receptor โ glucagon โ which is what appears to drive the additional fat-loss and hepatic-fat effects observed in phase-2 trials.
The molecule is engineered with a fatty-acid side chain that binds albumin, extending its half-life to roughly six days โ long enough for a single weekly dose to maintain steady exposure.
Most published protocols step from 2 mg โ 4 mg โ 8 mg โ 12 mg weekly, moving up every four weeks as GI tolerance allows.
Published research
New England Journal of Medicine, 2023
NEJM, 2023
Nature Medicine, 2024
Linked purely for research context. Sold for laboratory use only.
Often studied alongside
Retatrutide
$350 ยท 40 mg / vial