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Bacteriostatic Water 10ml

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AOD9604 6mg

AOD-9604, lipolytic peptide fragment, which was derived from human growth hormone (HGH) during the late 1990s was modified from HGH residues 176-191. This modified compound primarily works as an element for fat burning and obesity treatment, while the exact mechanism by which this happens is still under research. It stimulates the breakdown (metabolism) of fat stores and inhibits the formation of fats without any detected side effects, affecting blood sugar levels or causing abnormal growth. In addition, the peptide shows several, apparently independent, positive effects on cartilage regeneration, improvement of metabolism or heart activity, confirmed by research.

€37.99

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Molecular Formula:

Molecular Weight:

1815.1

Monoisotopic Mass:

1813.86035961

Polar Area:

815

Complexity:

3710

XLogP:

-4.8

Heavy Atom Count:

126

Hydrogen Bond Donor Count:

28

Hydrogen Bond Acceptor Count:

28

Rotatable Bond Count:

45

PubChem LCSS:

Aod-9604 Laboratory Chemical Safety Summary

Description of AOD-9604

A synthetically produced peptide AOD-9604 consists of 15 amino acids. It is derived fragment of human growth hormone (fragment 176-191) known mainly for its lipolytic qualities, thanks to which it can perfectly stimulate body fat burning without negative side effects, that are mainly perceived by using common weight loss drugs. Study has shown that it has a very good tolerability and safety, thus the immune system does not form any antibodies against the AOD-9604 peptide. Other great benefit seems to be that blood sugar levels are not affected. However, several studies have also shown that chronic treatment with AOD-9604 had no adverse effect on insulin sensitivity of researched animals. So, the peptide does not appear to affect IGF-1 or insulin levels at all.

Now we would like to bring you closer to the effects of the peptide, which have been researched and confirmed in studies.

[1] [2]

Research Confirmed Effects

1. Lipid Metabolism & Adipose Biology in Preclinical Models

AOD9604 has been evaluated in animal models and in mechanistic study designs that quantify lipid-metabolism–associated readouts, including changes in lipid handling markers and adipose-tissue–linked endpoints under controlled dosing paradigms. Comparative studies have also examined AOD9604 alongside full-length hGH to differentiate fragment-driven activity profiles from broader somatotropic signaling frameworks.

2. Receptor-Pathway Independence Testing in Genetic Models

Preclinical studies have used genetic mouse models (including β3-adrenergic receptor knock-out designs) to evaluate whether lipid-metabolism–linked readouts observed with AOD9604 are maintained when specific adrenergic signaling components are absent. These designs are used to support hypothesis generation regarding pathway attribution and to refine mechanistic models of lipid mobilization in vivo.

3. Joint Tissue Biology in Osteoarthritis-Associated Animal Models

AOD9604 has been investigated in rabbit osteoarthritis models using intra-articular experimental designs, including conditions with and without hyaluronic acid. These studies quantify preclinical endpoints relevant to joint-tissue response and structural pathology within the constraints of the model system, supporting laboratory investigation of cartilage-associated signaling environments and matrix remodeling biology.

4. Cardiometabolic Biomarker Mapping in Mechanistic Frameworks

Reviews discussing obesity-related research compounds have considered mechanistic relationships between adipose biology, lipid handling, and downstream cardiometabolic biomarker panels in preclinical settings. In RUO workflows, AOD9604 can be used as a probe within such frameworks to examine how modulation of lipid metabolism correlates with selected pathway-level markers under controlled experimental conditions.

Pathway / Mechanistic Context

AOD9604 is used in mechanistic study designs to map signaling and biochemical endpoints associated with lipid metabolism and adipose tissue function. Experimental readouts may include changes in lipid turnover markers, adipocyte-associated transcriptional programs, and pathway-proximal signals linked to nutrient handling. Comparative designs may include full-length hGH as a reference ligand to contextualize fragment-derived effects within broader somatotropic signaling networks, while avoiding confounding interpretation from pleiotropic endocrine pathways.

Preclinical Research Summary

Preclinical investigations have assessed AOD9604 in obese mouse models and in β3-adrenergic receptor knock-out mice, using lipid-metabolism endpoints and body composition–adjacent measurements to support mechanistic hypothesis testing regarding adipose biology pathways.

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Sergii

07.12.2025

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AOD9604 6mg

€37.99

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