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AOD-9604 — 5mg

$65.00Price
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Research-grade AOD-9604, a synthetic 16-amino-acid peptide fragment (Tyr-hGH 176-191) derived from the C-terminal domain of human growth hormone. Studied for selective lipolytic activity, adipose metabolism, and fat cell signaling independent of IGF-1 receptor activation. 5mg lyophilized powder, 99%+ purity verified by Janoshik Analytical via HPLC and mass spectrometry.


  • For laboratory research use only.

  • Not for human or veterinary use.

  • Not intended for diagnosis, treatment, cure, or prevention of any disease.

  • Use only in controlled laboratory settings by qualified personnel following appropriate safety procedures.

  • AOD-9604 (Anti-Obesity Drug 9604) is a synthetic hexadecapeptide corresponding to residues 176-191 of human growth hormone, with a tyrosine substitution at the N-terminus and an intramolecular disulfide bridge (Cys7-Cys14). Originally developed by Metabolic Pharmaceuticals Ltd. in Australia during the 1990s, AOD-9604 was designed to isolate growth hormone's lipolytic properties while excluding the broader metabolic and growth-promoting effects associated with full-length hGH. It completed six human clinical trials involving over 900 participants. AOD-9604 is frequently studied alongside Durham Peptides' metabolic research compounds including Semaglutide and Tirzepatide.


    BENEFITS


    • Selective lipolytic activity — studied for fat metabolism independent of IGF-1 receptor activation

    • Growth hormone fragment — retains the hGH 176-191 lipolytic region without somatotropic effects

    • Disulfide-stabilized — Cys7-Cys14 bridge provides conformational stability

    • Extensive clinical history — studied in over 900 human subjects across Phase I-IIb trials

    • Distinct mechanism — operates independently of the hGH receptor


    WHAT RESEARCHERS LOOK AT


    • β₃-adrenergic receptor upregulation in adipocyte models

    • Lipolysis and lipogenesis inhibition in white and brown adipose tissue

    • Comparative analysis vs. full-length hGH on lipolytic activity

    • IGF-1 independence and selective metabolic effects

    • Cartilage regeneration and joint biology in preclinical models

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