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Research compoundMetabolic ResearchAOD9604In stock

AOD-9604

A synthetic 16-amino-acid peptide based on the tail end (C-terminal region) of human growth hormone. It was studied in rodents around 2000 and in six human safety trials by an Australian developer; little new peer-reviewed work has appeared since.

Evidence: limited · Rodent studies plus published human safety trials

At a glance

Class
Synthetic 16-amino-acid peptide (hexadecapeptide)
Developer
Metabolic Pharmaceuticals (Australia)
FDA status
Not approved by the FDA for any use
Human data
Published human safety data exist (pooled analysis, 2013); not summarized on this page.
Animal / lab data
Zucker rat and ob/ob mouse studies (2000–2001); receptor-binding cell assays

Where it’s been studied

123
  • 1Adipose tissueZucker (fa/fa) rats (2000); ob/ob (leptin-deficient) mice (2001)
  • 2Blood glucose and lipidsPlasma glycerol and glucose, ob/ob mice (2001)
  • 3Receptor bindinghGH-receptor-transfected cells (2001)

Mechanism studied

In mouse and cell studies, AOD9604 did not compete for the growth hormone receptor and did not trigger cell proliferation, unlike full growth hormone [2]. In ob/ob mice it increased fat oxidation and plasma glycerol, a marker of fat breakdown [2]. It raised expression of the beta-3 adrenergic receptor in fat, but mice lacking that receptor still showed acute increases in energy expenditure, so the exact pathway remains unresolved [3].

What the research shows

StudyModelReported resultSource
Ng et al., metabolic study [1]Rat
Zucker (fa/fa) rats, 19 days, vs untreated controls
Researchers measured lipolytic activity in adipose tissue and insulin sensitivity (clamp) versus untreated controls.Peer-reviewed
Horm Res 2000
Heffernan et al., fat oxidation [2]Mouse
ob/ob and lean mice, 14 days, compared with full hGH; plus receptor-binding cell assay
Reduced weight gain and raised fat oxidation and plasma glycerol; unlike hGH, no rise in blood glucose and no hGH-receptor bindingPeer-reviewed
Int J Obes 2001
Beta-3 receptor knockout study [3]Mouse
ob/ob mice and beta-3 adrenergic receptor knockout mice, 14 days
Raised beta-3 receptor RNA toward lean-mouse levels; chronic weight effect absent in knockout mice, acute energy expenditure increase retainedPeer-reviewed
Endocrinology 2001
Pooled human safety analysis [4]Human
Six randomized, double-blind, placebo-controlled trials (phase 1 to 2b), 893 adults, up to 24 weeks
Endpoints: safety and tolerability, including IGF-1, glucose tolerance and anti-drug antibodies. PublishedPeer-reviewed
J Endocrinol Metab 2013
Preclinical safety review [5]Review
Summary of genotoxicity tests and repeat-dose studies in rats and monkeys (unpublished GLP reports)
Collects the developer's toxicology program; underlying reports are not individually peer reviewedPeer-reviewed
J Endocrinol Metab 2014

Human trials are listed for research context only; outcomes are reported in the linked publications. Animal and lab results do not establish effects in humans.

Verified by third-party testing

CertificatePosted on the product page
TestingIndependent, third-party

Research-grade supply

PureLab supplies AOD-9604 for laboratory research. Lot-specific certificates of analysis are posted on the product page as they are issued.

View research-grade AOD-9604

More in Metabolic Research

Sources

  1. Ng FM et al. (2000). doi:10.1159/000053183 Source
  2. Heffernan M et al. (2001). doi:10.1038/sj.ijo.0801740 Source
  3. Heffernan M et al. (2001). doi:10.1210/endo.142.12.8522 Source
  4. Stier H et al. (2013) Source
  5. Moré MI et al. (2014). doi:10.14740/jem213w Source
For research use only. Not for human or veterinary use. Not a drug, food or cosmetic, and not intended to diagnose, treat, cure or prevent any disease. This library summarizes published research for educational purposes. PureLab Performance Inc.