New — Free Peptide Starter Guide (2026): 13 chapters, 34 cited studies

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ToolsCompareAdipotide vs Dermorphin

Adipotide vs Dermorphin

Side-by-side comparison of key properties, dosing, and research.

Fat Loss & Metabolic
Adipotide
Recovery & Repair
Dermorphin
Summary
Adipotide (FTPP) is a chimeric proapoptotic peptide that selectively targets and destroys blood vessels feeding white adipose tissue. It binds prohibitin on the vasculature of fat tissue, delivering a proapoptotic sequence that induces cell death in fat-specific blood vessels, causing targeted fat tissue regression.
Dermorphin is a naturally occurring heptapeptide opioid isolated from the skin of South American phyllomedusine frogs. It is one of the most potent endogenous mu-opioid receptor agonists known, approximately 30-40 times more potent than morphine by weight. Explored for pain management and fatigue modulation.
Half-Life
Estimated 2-4 hours
Estimated 30-60 minutes (longer than endorphins due to D-Ala)
Admin Route
Subcutaneous, Intravenous (research)
Subcutaneous (research), Intrathecal (research), Intranasal (research)
Research
Typical Dose
Not established for humans; primate studies used 0.1-1 mg/kg
Not established for human use; research doses vary widely
Frequency
Daily for 4 weeks (research protocol)
Not established
Key Benefits
  • Targeted reduction of white adipose tissue
  • Promotes fat vasculature apoptosis without systemic toxicity
  • Demonstrated significant fat loss in primate studies
  • Potential for visceral and subcutaneous fat reduction
  • Novel non-hormonal mechanism distinct from GLP-1 agonists
  • Explored for obesity and metabolic syndrome
  • Potent analgesia superior to morphine on a per-weight basis
  • May reduce perception of fatigue in high-intensity activity
  • Longer-lasting than endogenous opioids due to D-amino acid substitution
  • Research tool for mu-opioid receptor pharmacology
  • Potential therapeutic application in refractory pain
Side Effects
  • Renal toxicity observed in primate studies (transient, dose-dependent)
  • Dehydration and electrolyte imbalances in research
  • Weight regain upon cessation
  • Limited human data; side effect profile largely from animal studies
  • High addiction and dependence potential (mu-opioid agonism)
  • Respiratory depression at high doses
  • Nausea, vomiting, constipation
  • Sedation and cognitive impairment
  • +2 more
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