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Evidence: CCognitive EnhancementLongevity

Pinealon: Benefits, Dosage & FDA Status

Pinealon (EDR)

A short tripeptide developed in Russia for cognitive aging and oxidative stress. Limited Western clinical evidence.

FDA Status

Not FDA-approved — Russian-origin research peptide

Typical Dose

5–10 mg daily for 10–20 days (subcutaneous, cycled)

Evidence Grade

CPrimarily preclinical or anecdotal

Half-Life

Minutes

Routes of Administration

subcutaneous, intranasal

First Synthesized

2000s

Clinics Indexed

9 providers have offered Pinealon in our tracked directory.

Mechanism of Action

EDR tripeptide reported to penetrate BBB, modulate gene expression, and reduce neuronal oxidative damage.

Key Reported Benefits

Benefits listed reflect commonly reported effects from clinical trials and practitioner use. Individual response varies. Evidence-grade C indicates primarily preclinical or anecdotal.

Reported Side Effects

  • Generally well-tolerated

Contraindications

  • Pregnancy

Commonly Stacked With

Regulatory & Safety Context

FDA status: Not FDA-approved — Russian-origin research peptide

This page is for educational purposes only and does not constitute medical advice. Peptide use outside of an FDA-approved indication should be discussed with a licensed medical professional. Source quality, cold-chain storage, and injection hygiene all materially affect safety outcomes.

See state-by-state legality: US peptide legality by state →

References

Selected primary literature on Pinealon. Full PubMed records linked. Additional citations are available on request.

  1. PubMed PMID 22039583

Last reviewed: 2026-04-30

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