99%+ Purity

AOD-9604

Modified HGH fragment

CAS Number

221231-10-3

Molecular Weight

1815.08 g/mol

Available Forms
Lyophilized Powder
Available Sizes
2mg5mg10mg

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99%+ Purity

HPLC verified purity standards

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Research Areas
Lipolysis ResearchAdipose MetabolismBody CompositionMetabolic Studies

Modified HGH fragment for metabolic research. AOD-9604 is a synthetic peptide fragment of human growth hormone (hGH 176-191) studied for its effects on fat metabolism without the growth-promoting effects of full HGH.

AOD-9604 Research Compound

Research Use Only

This product is intended for laboratory research purposes only. It is not intended for human or veterinary use, food, cosmetic, household, or agricultural applications. Not for human consumption.

Overview

AOD-9604 (Anti-Obesity Drug-9604) is a synthetic peptide fragment corresponding to the C-terminal portion of human growth hormone (amino acids 176-191). Developed by Metabolic Pharmaceuticals, this modified fragment was designed to retain the fat-reducing properties of HGH while eliminating its growth-promoting and diabetogenic effects. Although clinical trials for obesity treatment did not meet primary endpoints, AOD-9604 remains an active research compound for studying fat metabolism mechanisms.

Molecular Characteristics

PropertyValue
Molecular FormulaC78H123N23O23S2
Molecular Weight1815.08 g/mol
CAS Number221231-10-3
SequenceTyr-Leu-Arg-Ile-Val-Gln-Cys-Arg-Ser-Val-Glu-Gly-Ser-Cys-Gly-Phe
Amino Acids16
StructureContains disulfide bridge (Cys⁷-Cys¹⁴)
Purity≥99% (HPLC)

Mechanism of Action

AOD-9604 affects lipid metabolism through specific pathways:

Lipolytic Activity

  • Stimulation of lipolysis in adipose tissue
  • Activation of beta-3 adrenergic receptors
  • Hormone-sensitive lipase (HSL) activation
  • Free fatty acid release enhancement

Anti-Lipogenic Effects

  • Inhibition of lipogenesis
  • Reduction of fat accumulation
  • Modulation of fatty acid synthase
  • Altered adipocyte metabolism

Distinct from Full HGH

  • No IGF-1 elevation
  • No hyperglycemic effects
  • No growth promotion
  • Limited to C-terminal region activity

Potential Additional Effects

  • Cartilage regeneration research
  • Osteoarthritis models
  • Tissue repair studies

Research Applications

Adipose Tissue Research

  • Lipolysis mechanism studies
  • Adipocyte function research
  • Fat depot differences
  • Obesity models

Metabolic Studies

  • Energy expenditure research
  • Substrate oxidation
  • Metabolic rate assessment
  • Insulin sensitivity effects

Body Composition

  • Fat mass reduction models
  • Lean mass preservation studies
  • Regional fat distribution
  • Long-term effects

Cartilage/Joint Research

  • Chondrocyte studies (GRAS status in Australia)
  • Osteoarthritis models
  • Cartilage repair mechanisms

Available Formats

SizeFormatCatalog Code
2mgLyophilizedAOD-2
5mgLyophilizedAOD-5
10mgLyophilizedAOD-10

Handling & Storage

  • Store lyophilized peptide at -20°C
  • Protect from light and moisture
  • Reconstitute with bacteriostatic water
  • Reconstituted solution stable at 2-8°C for up to 3 weeks
  • Contains disulfide bridge (avoid reducing agents)
  • Avoid repeated freeze-thaw cycles

Quality Specifications

  • Purity: ≥99% by HPLC
  • Appearance: White lyophilized powder
  • Solubility: Soluble in water
  • Disulfide Bridge: Intact (verified)
  • Endotoxin: Less than 1 EU/mg
  • Certificate of Analysis provided

Clinical Trial History

PhaseOutcome
Phase ISafety established
Phase IIaPositive signals
Phase IIb/IIIDid not meet primary endpoint for obesity
CurrentResearch continues; GRAS for joint health (Australia)

References

  1. Heffernan MA, et al. "The effects of human GH and its lipolytic fragment (AOD9604) on lipid metabolism following chronic treatment in obese mice and rats." Endocrinology. 2001.
  2. Ng FM, et al. "Metabolic studies of a synthetic lipolytic domain (AOD9604) of human growth hormone." Horm Res. 2000.
  3. Stier H, et al. "AOD9604, a synthetic C-terminal fragment of human growth hormone: a phase II study in obese patients." Int J Obes. 2008.

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