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Adipotide (FTPP)

Adipotide is a ligand-directed peptidomimetic: a cyclic CKGGRAKDC motif binds prohibitin on the endothelial cells that line white-adipose-tissue blood vessels, and a fused proapoptotic D(KLAKLAK)2 sequence disrupts mitochondrial membranes once internalized. This triggers apoptosis of the fat's vascular supply, producing ischemic atrophy of white fat depots rather than appetite suppression. The same delivery to renal tissue underlies the dose-dependent, reversible kidney effects seen in primates.

Molecular Profile
linear
25 AA Sequence
Evidence grade (Preclinical): Animal or in-vitro studies; no controlled human trials. This grade reflects the overall quality of available research on this compound and does not constitute a clinical recommendation.
CAS
859216-15-2
Mol. weight
2557.2 g/mol
Formula
C111H206N36O28S2
Chain length
25 aa
Sequence
CKGGRAKDC-GG-(D)(KLAKLAK)2 (cyclic targeting motif + proapoptotic D-peptide)
Onset and duration

Metabolic effects build over days to weeks of consistent use.

Storage and reconstitution

Store the lyophilized powder refrigerated (2 to 8 C), or frozen for long-term storage, protected from light. After reconstitution with bacteriostatic water, keep refrigerated and use within about 4 weeks.

Clinical Evidence

What the literature says

Scientific Overview

According to PubMed, adipotide induced targeted apoptosis in white-fat blood vessels and produced rapid weight loss and improved insulin resistance in obese Old World monkeys, but at higher doses caused predictable, reversible renal proximal-tubule changes (Barnhart KF et al., Sci Transl Med 2011). Human data are limited to a Phase 1 dose-finding/safety study (NCT01262664) in patients with obesity and metastatic prostate cancer; development has not advanced publicly. It is investigational only.

Pharmacokinetics

Routes
Subcutaneous

Last reviewed: 2026-06-15

Research Guide

How users approach this compound

The following reflects patterns observed in research literature and community protocols. This is not medical advice and does not constitute a clinical recommendation.

Typical Dose Range Observed

0.03 mg
0.03 mg/kg once daily subcutaneous (Phase 1)

Research Protocols

Common Dosages

Phase 1 (human, safety)

0.03 mg/kg
Once daily SC for 28 days

Dose-finding/safety only (NCT01262664); investigational

Dosages listed are common research protocols found in peer-reviewed literature and clinical trials. Individual results and requirements may vary significantly in a research context.

Reported Uses

Key Research Benefits

  • Preclinical: targeted destruction of white-fat vasculature causing fat loss
  • Preclinical: weight loss and improved insulin resistance in obese monkeys
  • Mechanistically distinct from appetite-based fat-loss agents

Potential Side Effects

Reversible kidney (renal proximal tubule) dysfunction at higher doses
Injection-site effects
Long-term human safety unknown

Considerations and Cautions

  • No established human safety; not for use outside research
  • Renal impairment (dose-dependent renal toxicity seen in primates)
  • Pregnancy or breastfeeding (no data)

Labs to monitor

Educational context only, not a testing mandate. Any bloodwork decisions belong with your clinician.

Dose Calculator

Peptide Reconstitution Calculator

mg

Total amount of peptide in the vial.

mL

Volume of water used to mix.

mcg

Draw to this mark

10 Units

or 0.10 mL on a U-100 syringe

Concentration:2.50 mg/mL
Peptide per Unit:25.00 mcg/unit
*Always double-check your calculations. This tool is for educational purposes only.

Adipotide (FTPP) by goal

Read Adipotide (FTPP)'s profile filtered through specific research goals.

Related Tools

Not medical advice

Information on DoseVault is for educational purposes only and is not a substitute for medical advice, diagnosis, or treatment from a qualified healthcare provider.