peptides
R E T A 40mg
R E T A is a GLP-3 class research peptide investigated in laboratory models for incretin-pathway signaling, energy expenditure, and body-composition endpoints. Supplied lyophilized at 99%+ HPLC purity.
Research-observed benefits
- ›GLP-3 class incretin signaling
- ›Body-composition endpoints
- ›Energy-expenditure research
- ›Glycemic-marker models
Findings reported in in-vitro / preclinical research literature. Not therapeutic claims.
CAS Number
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Purity
99%+
Molecular Formula
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Stock
500 units
Order type
Purchase option
Quantity
Total
$110
For in-vitro research only. Not for human consumption, diagnostic, or therapeutic use. Storage at -20°C recommended for lyophilized peptides.
R E T A 40mg — Full Research Breakdown
Tailored information for researchers. All content is for in-vitro / preclinical research context only — not medical advice.
Mechanism of Action
GLP-3 class multi-receptor incretin agonist. Engages incretin and glucagon-family receptors simultaneously, combining satiety and insulinotropic signaling with increased energy expenditure in laboratory models.
How It Helps
The multi-receptor profile is why researchers use it to model body-composition and metabolic-rate endpoints that single-receptor agonists do not reproduce.
Half-Life
Long-acting; supports weekly intervals in study designs
Onset of Effects
Metabolic-marker shifts commonly observed within 2–4 weeks in model systems.
Storage
Lyophilized: –20°C. Reconstituted: 2–8°C, 28 days. Protect from light.
Stacks Well With
- ›Cagrilintide (amylin satiety pathway)
- ›Tesamorelin (body composition)
Research-Observed Side Effects
- •Nausea
- •Reduced appetite
- •Transient GI discomfort
- •Injection-site reaction
Translational Cautions
- •Gastroparesis models
- •Prior sensitivity to incretin analogs
Research Highlights
- ▸Multi-receptor agonism produces larger composition changes than single-pathway comparators in published models.
- ▸Glucagon-receptor engagement is associated with increased energy expenditure alongside appetite suppression.
- ▸Titration-style designs are used to characterize tolerability across concentrations.