GLP's ⏱ Half-life: ~10-30 minutes

Peptide YY

Peptide YY (PYY / Peptide Tyrosine Tyrosine)

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Half-Life
~10-30 minutes
Purity
≥95%
Mol. Weight
4,049.55 Da
Form
Lyophilized powder

What is Peptide YY?

Peptide YY is a key satiety hormone released from the gut after eating. It plays a central role in the “gut-brain axis” that controls appetite. Research interest centers on its potential as a therapeutic target for obesity, either through direct administration or by enhancing endogenous PYY release through dietary interventions.

Dosage Information (Research Use)

Research doses: IV infusion at 0.8 pmol/kg/min in clinical studies. No standardized subcutaneous dosing established. Research compound only.

Reconstitution & Handling

Reconstitute with sterile water per manufacturer instructions.

Half-Life & Pharmacokinetics

~10-30 minutes

Reported Observations in Literature

Nausea at higher doses, transient increase in heart rate, abdominal discomfort. Generally well-tolerated in research settings at physiological doses.

Key Research References

  • Batterham RL et al. “Gut hormone PYY3-36 physiologically inhibits food intake.” Nature. 2002;418:650-4

How Peptide YY Works

Peptide YY (PYY) is released from intestinal L-cells after meals, acting on Y2 receptors in the arcuate nucleus of the hypothalamus to suppress appetite. PYY3-36, the primary circulating form, crosses the blood-brain barrier and directly inhibits NPY/AgRP neurons while activating POMC/CART neurons. It also slows gastric emptying and reduces gastric acid secretion.

Research Applications

🔬 Obesity and weight management
🔬 Appetite regulation and satiety
🔬 Type 2 diabetes and metabolic syndrome

Research Findings

Infusion studies show PYY3-36 reduces caloric intake by ~30% in both lean and obese individuals. Obese subjects have lower baseline PYY levels, suggesting a physiological role in obesity. Combination approaches with GLP-1 agonists show additive appetite suppression.

Dosage & Administration

Research doses: IV infusion at 0.8 pmol/kg/min in clinical studies. No standardized subcutaneous dosing established. Research compound only.

Safety & Side Effects

Nausea at higher doses, transient increase in heart rate, abdominal discomfort. Generally well-tolerated in research settings at physiological doses.

Important: All safety information is derived from published research, primarily animal studies. No controlled human clinical trial data exists unless explicitly noted. This compound is sold for research purposes only.

Quick Facts

Molecular Weight 4,049.55 Da
Half-Life ~10-30 minutes
Purity ≥95%
Form Lyophilized powder
Storage Lyophilized: -20°C. Reconstituted: 2-8°C.

Key Research References

  • Batterham RL et al. "Gut hormone PYY3-36 physiologically inhibits food intake." Nature. 2002;418:650-4

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