Adipotide
Also known as FTPP, Prohibitin-targeting peptide 1, CKGGRAKDC-GG-D(KLAKLAK)2
A preclinical pro-apoptotic peptidomimetic that homes to white-fat blood vessels and triggers their death, causing fat loss in animal studies — but with dose-limiting kidney toxicity.
Typical use cases
Dosing guidelines
Titration
Typically flat-dosed in short cycles (e.g. ~28 days) in animal studies; no human titration scheme exists.
Reconstitution
10 mg vial: add ~2 mL bacteriostatic water (~5 mg/mL); swirl gently.
Injection sites
Subcutaneous, rotate sites (abdomen/thigh) — route used in animal research.
Storage & handling
Lyophilized: stable months cool/dark, longer frozen. Reconstituted: refrigerate (2–8 °C).
Side effects
- Renal tubular toxicity (proteinuria/glucosuria)
- Dehydration / increased urination
- Injection-site reaction
- Electrolyte disturbance
Research summary
Adipotide (FTPP) is a chimeric peptide joining a prohibitin/annexin-A2 homing domain (CKGGRAKDC) to a pro-apoptotic D-peptide that disrupts mitochondrial membranes in the endothelium of white adipose tissue, pruning the fat's blood supply. In a 2011 obese-rhesus-monkey study animals lost roughly 10% body weight over ~28 days with improved insulin sensitivity; earlier work showed similar effects in obese mice. Evidence is entirely preclinical (mouse and non-human primate) — there are no completed human efficacy trials, and studies documented dose-dependent renal tubular changes (proteinuria, glucosuria) that flag a narrow therapeutic window. Educational only — not medical advice.
Key references
- Kolonin et al., Nature Medicine (2004) — adipose vasculature-targeting peptide in obese mice
- Barnhart et al., Science Translational Medicine (2011) — adipotide causes weight loss in obese monkeys
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Educational reference only — not medical advice. Dosing figures are commonly-cited ranges, not prescriptions. Consult a qualified clinician.
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