Weight Management

Adipotide

CKGGRAKDC-GG-D(KLAKLAK)2 · Prohibitin-targeting peptide · fat-destroying peptide

Adipotide is a radically aggressive, experimental peptidomimetic engineered to physically eradicate white adipose tissue. Rather than simply suppressing appetite like a GLP-1, it is designed to assassinate the very blood supply feeding fat cells. While it demonstrated shockingly rapid and massive fat loss in primate models, it is essentially a highly targeted biological weapon that carries profound, severe risks of renal toxicity and kidney damage.

Not FDA-approved - research chemical
Reviewed by CalcMyPeptide Editorial Team
Last updated: August 2026Evidence: Low1 peer-reviewed citation
Typical research dose
0.5-1 mg/kg (research)
Frequency
Per study protocol
Half-life
Short - minutes to hours
Common vials
5 mg
Molecular weight
~3200 Da (estimated)

Use-case scores

0–10 against the evidence we have, not a gym ranking. Hidden domains do not apply here.

  • Metabolic / weight1.5/10

    Primate fat-loss plus renal toxicity in the published file. Not a cutting peptide. Mechanism with a hard safety haircut.

Compound card

Class
Prohibitin-targeting peptidomimetic (CKGGRAKDC-GG-D(KLAKLAK)2 class)
Formula
Custom pro-apoptotic peptide
Status
Not FDA-approved · research use
Dose it
5 mg + 2 mL BAC water → 2.5 mg/mL · 500 mcg ≈ 20 units (U-100)
Open in calculator

How it works

Adipotide (CKGGRAKDC-GG-D(KLAKLAK)2) is a pro-apoptotic peptide that selectively targets the vasculature feeding white adipose tissue. It binds to prohibitin on the surface of fat blood vessels and delivers a cell-killing D(KLAKLAK)2 sequence, causing mitochondrial disruption and apoptosis of the endothelial cells supplying fat depots. This cuts off nutrient supply to adipocytes, causing fat cell death and rapid weight loss. Phase I/II primate studies showed 11% body weight reduction over 4 weeks - one of the most aggressive mechanisms of any anti-obesity agent.

Source: PMID: 22100857

Research Use Cases

  • ✓Obesity (Preclinical Only): High

Dosing

PhaseDoseFrequencyNotes
Primate Research Dose~35 mg/kgDaily for 4 weeks (IV, primate model)No human clinical dose established. Research use only.

Administration

Route / form
Intravenous or subcutaneous (preclinical)
Timing
No established human protocol
Empty stomach?
No - Food timing is not critical.

Timeline

Week 1-4 (primate)
~11% body weight loss in obese rhesus monkeys. Rapid with renal toxicity signals at high doses.

Who it is for

Obesity (Preclinical Only)

High

Dramatic fat loss via vascular apoptosis mechanism - but renal toxicity observed in primates at therapeutic doses.

Reconstitution

VialWaterConcentrationExample dose
5 mg lyophilized2 mL BAC2.5 mg/mLDo not community-dose this. Identity only.

Change vial size or water volume? Open the reconstitution calculator.

Safety & Considerations

RESEARCH ONLY. Renal toxicity observed in primate studies at effective doses. No human clinical trials have been approved. Not for human use.

Regulatory & Legal Status

FDA Status (US)
Research Only
WADA Status (2026)
Not Listed

Not currently on the WADA 2026 Prohibited List. Policies may change - verify before competition.

Classification

Research Chemical

US Compounding: Not eligible / not available

⚠️ This information is for educational purposes only and may not reflect the most current regulatory updates. Always verify with official FDA, WADA, and jurisdiction-specific sources before use.

Limits of current evidence

  • Renal injury is the reason this is not a toy.
  • This site will not treat obesity from an adipotide page.

Verdict

Adipotide is a targeted pro-apoptotic peptidomimetic aimed at white-fat vasculature. Kidney toxicity showed up in animals. It is not a consumer fat-loss peptide.

Interactions & Contraindications

RESEARCH ONLY. Renal toxicity observed in primate studies at effective doses. No human clinical trials have been approved. Not for human use.

Frequently Asked Questions

Has adipotide been tested in humans?▼
No. Phase I primate studies showed significant weight loss but also renal toxicity at therapeutic doses, which has limited progression to human trials.
How does adipotide differ from GLP-1 drugs?▼
GLP-1 agonists suppress appetite centrally. Adipotide physically destroys the blood vessels feeding fat tissue via targeted apoptosis - a completely different and more aggressive mechanism.

References

  1. Kim DH et al. “"Targeted elimination of senescent cells by adipotide".” Science Translational Medicine (2011).

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