★ Metabolic

Adipotide

Metabolic · 2mg × 10 vials

Vascular-homing peptidomimetic studied for targeted apoptosis of adipose endothelium in primate models. Development halted for renal toxicity.

✓ 99%+ Purity ✓ Lab Tested ✓ COA on Request ✓ Discreet Shipping ✓ Direct Support
📋 Certificate of Analysis Request the third-party COA via Telegram
Pricing
$180from · 10-vial kit
Shipping: $40 US · $60 international (10-vial kits only) · single vials $20, US only · free over $1,000
2mg × 10 vials$180
5mg × 10 vials$345
Order / Consult on Telegram →
short (hours, exact human PK not published)
Half-life
fat-loss
Class
Overview

What Is Adipotide?

Adipotide (also called FTPP, Fat-Targeting Proapoptotic Peptide, or Prohibitin-Targeting Peptide 1) is a synthetic chimeric peptidomimetic with two domains joined together. The N-terminal CKGGRAKDC sequence is a vascular homing peptide that binds prohibitin-1 and annexin A2 on the endothelial cells lining the blood vessels that supply white adipose tissue. Once the peptide docks and is internalised, the C-terminal D(KLAKLAK)2 sequence, built from D-amino acids for protease resistance, inserts into the mitochondrial outer membrane of those endothelial cells, disrupts membrane integrity, releases cytochrome c, and triggers caspase-driven apoptosis.

The endothelial cells die, the capillary bed supplying that fat depot collapses, and the downstream adipocytes die from ischaemia. The mechanism is therefore targeted destruction of the vascular scaffolding fat depends on, not direct killing of fat cells. In the 2011 Science Translational Medicine primate study from the Arap and Pasqualini laboratory, obese rhesus monkeys lost about 11% of body weight over four weeks.

The critical limitation is that prohibitin is not exclusive to adipose vasculature. It is also expressed on the endothelium of renal vasculature, particularly the proximal tubule, so the same apoptotic mechanism damages renal capillaries and produces tubular toxicity, proteinuria, and rising creatinine. The therapeutic window between adipose-vessel ablation and renal injury proved narrow in primates, and the Phase 1 human trial at MD Anderson was terminated for renal toxicity.

Published Safety Data

What the published studies measured.

What the studies show
Measured in clinical trials
  • Nephrotoxicity: dose-dependent renal tubular changes in primates including increased serum creatinine, decreased phosphorus and potassium, glucosuria, proteinuria, and increased transitional/renal epithelial cells in urine. In primate studies these were characterized as "mild, predictable, and reversible". In human Phase 1 (NCT01262664) the renal findings were unacceptable and the trial was terminated. No published human safety data otherwise.
  • Weight loss: 7-15% body weight reduction over 28 days in primate cohorts (mean ~10.6%), with ~38.7% reduction in total body fat
  • Insulin sensitivity improvement: significant in obese primates, glucose tolerance improvements occurred BEFORE measurable weight loss
  • Injection site reactions: not formally quantified, reported anecdotally outside trials
  • Human trial outcomes: NOT PUBLISHED beyond the termination notice. There is zero peer-reviewed human efficacy or safety data. This is the dominant evidence gap.
The Research

Peer-reviewed studies and clinical guidelines — tap any to read the source.

PubMed / Science TranslaBarbosa et al., A Peptidomimetic Targeting White Fat Causes Weight Loss and Improved Insulin Resistance in Obese Monkeys, 2011

pivotal primate study showing 10.6% weight loss and 38.7% fat loss over 28 days, with the renal toxicity signal characterized as mild and reversible

Read study ↗
PubMedResponse to Comment on Peptidomimetic Targeting White Fat, Science Translational Medicine 2012

Pasqualini/Arap response to early renal safety critiques

Read study ↗
ClinicalTrials.govNCT01262664 — Phase I Evaluation of Prohibitin Targeting Peptide 1 in Patients With Metastatic Prostate Cancer and Obesity

trial terminated, no published results

Read study ↗
Physician/research summaSuperpower — A Proapoptotic Peptide Targeting Adipose Vasculature

clinical commentary on mechanism, evidence gap, and the nephrotoxicity bottleneck

Read study ↗

Reconstitution & Storage

Storage: refrigerated, ~14-21 days after reconstitution; freshness matters because the proapoptotic D(KLAKLAK)2 sequence can lose potency if degraded

All products sold for research purposes only. Not for human or animal consumption. Must be 18+ to purchase. By placing an order you confirm compliance with all applicable local laws and regulations.