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

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ToolsCompareAdipotide vs Thymagen

Adipotide vs Thymagen

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

Fat Loss & Metabolic
Adipotide
Immune Support
Thymagen
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.
Thymagen is a dipeptide bioregulator (Glu-Asp) developed by Professor Vladimir Khavinson, tissue-specific for the thymus gland. It supports T-lymphocyte maturation, thymic function, and immune system normalization. As the thymus involutes with age (thymic atrophy), immune competence declines. Thymagen is used to support immune restoration, particularly in aging, post-illness recovery, and immunodeficiency states.
Half-Life
Estimated 2-4 hours
Short (minutes); sustained gene-regulatory effects
Admin Route
Subcutaneous, Intravenous (research)
SubQ, Oral
Research
Typical Dose
Not established for humans; primate studies used 0.1-1 mg/kg
10 mg per day
Frequency
Daily for 4 weeks (research protocol)
Daily for 10–30 days
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
  • Supports thymic epithelial cell function and T-cell maturation
  • May partially restore thymic output reduced by age-related atrophy
  • Normalizes T-lymphocyte subpopulation balance
  • Supports immune recovery after illness, surgery, or chemotherapy
  • Anti-aging effects on thymic tissue
  • Complementary to Thymosin Alpha-1 and Thymalin in immune protocols
  • May improve vaccine responsiveness in older individuals
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
  • Generally well tolerated
  • Mild injection site reactions
  • No significant immunological adverse events reported
Stacks With