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Research monograph

Pinealon[Glu-Asp-Arg; EDR peptide]

Compound snapshot

Class

Research peptide

FDA approved

No

Clinical development

Phase 2

Last reviewed

September 2026

Research areas

Cognition / Mood / Neuroprotection

Regulatory status

Research use only — not approved

Internet attention

Moderate

Registry query

Pinealon

A synthetic three-amino-acid peptide from the Russian short-peptide bioregulator program, promoted for brain ageing and cognition. It has not been established as a medicine by major regulators.

Reality check — what we actually know

Supported by human evidence

  • No adequately powered randomised human trials establish the outcomes this compound is marketed for.

Animal research only

  • Reduced oxidative-stress markers and necrotic cell death in cultured neuronal and other cells
  • Improved selected learning and stress measures in limited rodent studies
  • Studied in aged-rat models of hypoxia and hypothermia

Mechanistically plausible

  • Cell studies report changes in reactive-oxygen-species accumulation, ERK signalling and cell-cycle activity. Broader claims that the tripeptide directly regulates specific genes remain speculative and have not been independently validated.

Common internet claims

  • Online discussion frequently presents Pinealon as a proven treatment rather than a research compound.

Not established

  • Human efficacy for the outcomes commonly claimed
  • Optimal route, quantity and duration in humans
  • Long-term human safety

Evidence distribution

Each band is a live PubMed search for Pinealon, filtered to that kind of study. Top is the strongest evidence; the base is reasoning, not proof. A band with no records means that kind of study has not been published for this compound yet.

Mechanism and reported findings

Cell studies report changes in reactive-oxygen-species accumulation, ERK signalling and cell-cycle activity. Broader claims that the tripeptide directly regulates specific genes remain speculative and have not been independently validated.

  • Reduced oxidative-stress markers and necrotic cell death in cultured neuronal and other cells
  • Improved selected learning and stress measures in limited rodent studies
  • Studied in aged-rat models of hypoxia and hypothermia

Strength of the evidence: Very low certainty. Evidence is limited to cell and animal studies, much of it from the originating research network and Russian-language journals. No controlled human trial establishes cognitive or longevity benefit.

Safety and known cautions

No approved indication, established human safety profile or independently confirmed mechanism. It should not replace evaluation for memory change, cognitive decline, depression or neurological symptoms.

Evidence at a glance

No single score, on purpose. The line beside each bar shows how much reported outcomes vary between studies.

Human studiesLimited
Animal studiesMultiple studies
Lab / in-vitroMultiple studies
Clinical efficacyNot established
Long-term safetyNot established

Development stage

  1. Discovery
  2. Preclinical
  3. Phase 1
  4. Phase 2Current
  5. Phase 3
  6. Regulatory review
  7. Approved
Registered trials on ClinicalTrials.gov →

Primary sources

Education only — research summary, not dosing advice. Approved medicines are prescription-only; investigational compounds are not approved for human use.
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