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Source comparison

AOD 9604 vs hGH vs Other Lipolytic Peptides

AOD 9604 Beta-3 adrenergic agonism Beta-3 adrenergic receptor None Neutral Isolated lipolysis studies without growth confounders hGH (191aa) GH receptor activation → JAK2-STAT5 → IGF-1 synthesis Growth hormone receptor Significant (2-3× baseline) Hyperglycaemi

This comparison does not assign a generated winner or score.

  • AOD 9604
  • Beta-3 adrenergic agonism
  • Beta-3 adrenergic receptor
  • None
  • Neutral
  • Isolated lipolysis studies without growth confounders
  • hGH (191aa)
  • GH receptor activation → JAK2-STAT5 → IGF-1 synthesis
  • Growth hormone receptor
  • Significant (2-3× baseline)
  • Hyperglycaemic (insulin resistance)
  • Anabolic signalling, IGF-1 pathway research
  • CJC-1295
  • GHRH analogue → pulsatile GH release
  • GHRH receptor (pituitary)
  • Moderate (pulsatile)
  • Variable (depends on GH response)
  • Physiological GH pulsatility models
  • Hexarelin
  • Ghrelin receptor agonist → GH secretion
  • GHSR-1a (ghrelin receptor)
  • Moderate
  • Orexigenic (appetite stimulation)
  • Ghrelin pathway and appetite regulation studies
  • Ipamorelin
  • Selective ghrelin receptor agonist
  • GHSR-1a
  • Mild
  • Minimal
  • GH secretagogue research with low side-effect profile
  • Bottom Line
  • AOD 9604 is the only option in this table that stimulates fat breakdown without activating growth hormone pathways. Making it ideal for lipolysis-specific protocols where IGF-1 or glucose confounders would invalidate results.
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