AOD-9604
Technical Monograph
AOD-9604 is a synthetic peptide fragment of the C-terminal region (residues 177-191) of human growth hormone (hGH). Equipped with a tyrosine substitution at the N-terminus to stabilize the molecule, it exclusively replicates the lipolytic properties of native hGH without conferring somatotropic or insulin-resistant side effects.
Mechanism of Action
AOD-9604 upregulates the expression of the strictly lipolytic β3-adrenergic receptors in adipose tissue. It intensely stimulates lipolysis and inhibits lipogenesis within adipocytes. It lacks the binding domains required for full GH receptors, producing no IGF-1 elevation.
Pharmacological Detail
Triggers downstream activation of hormone-sensitive lipase (HSL) primarily via targeted engagement with β3-adrenoreceptors.
Pharmacodynamics
Selectively acts upon adipose sites characterized by high beta-3 receptor density. Causes robust triglyceride hydrolysis.
Pharmacokinetics
Rapid plasma clearance with sustained metabolic transcription shifts persisting for 24-48 hours.
Preclinical Observations & In Vitro Data
Consistently demonstrated high-velocity weight loss in obese phenotype animal models without negative metabolic derangements.
Observed Timeline of Action
| Timeframe | Pharmacological Effect |
|---|---|
| 2-4 hours | Measurable uptick in systemic free fatty acid (FFA) mobilization. |
| Day 14 | Initial observable reduction in specific adipocyte volume via histology. |
Abstract Highlights
- Demonstrates isolated lipolytic activity strictly devoid of generalized anabolic effects
- Activates β3-adrenergic pathways directly within white adipose tissue
- Does not alter systemic glucose metabolism or insulin sensitivity
References
Chemical Specifications
Material Handling & Stability
Strict Notice
THIS COMPOUND IS PRODUCED FOR LABORATORY RESEARCH PURPOSES ONLY. NOT FOR HUMAN CONSUMPTION. MATERIAL DATA SHEETS AND LABORATORY GUIDELINES SHOULD BE CONSULTED PRIOR TO HANDLING.