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Research-onlyVendors pendingFacts verified · 2026-05-25

Pinealon

Also known as edr peptide · Wikipedia

Pinealon is a synthetic tripeptide with the sequence Glu-Asp-Arg (EDR), one of the short 'bioregulator' peptides from the Khavinson family developed at the St. Petersburg Institute of Bioregulation and Gerontology. It is marketed in Russian and Eastern European literature for cognitive support, neuroprotection, and memory, with most published evidence coming from a single research group. Mechanistic studies report reduced oxidative stress, decreased neuronal apoptosis, and modulation of gene expression including S100B and dendritic-spine recovery in Alzheimer's disease models. No FDA approval and no clinical trials are registered on ClinicalTrials.gov. Treat all efficacy claims with caution. Also known as: EDR peptide.

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Mechanism of action

Pinealon is the synthetic tripeptide Glu-Asp-Arg (EDR), one of the short 'bioregulator' peptides characterized by Khavinson and colleagues [Khavinson 2021, PMID 34071923]. The proposed mechanism is direct sequence-specific binding to gene-promoter regions to modulate transcription of neuroprotective factors including S100B [Ilina 2020, PMID 33396470].

Pinealon is the synthetic tripeptide Glu-Asp-Arg (EDR), one of the short 'bioregulator' peptides characterized by Khavinson and colleagues [Khavinson 2021, PMID 34071923]. The proposed mechanism is direct sequence-specific binding to gene-promoter regions to modulate transcription of neuroprotective factors including S100B [Ilina 2020, PMID 33396470]. Preclinical studies in cerebellar granule cells, PC12 cells, and primary hippocampal neurons report dose-dependent suppression of ROS, reduced caspase-3 activation, and preservation of mitochondrial membrane potential under oxidative or amyloid-beta stress [Khavinson 2011, PMID 21978084]. In 5xFAD Alzheimer mouse models, EDR restored mushroom dendritic spines toward normal density. The receptor target has not been validated by independent Western pharmacology.

Pharmacokinetic properties

Half-life

unknown (no rigorous human PK data published)

Routes

intramuscular · subcutaneous · oral · intranasal

Bioavailability

Khavinson group claims oral bioavailability; no Western PK validation. Small tripeptide size may permit some intestinal absorption but data is sparse.

Amino-acid sequence

Glu-Asp-Arg

Use & research dosing

No FDA-approved dose exists (research framing only). Self-experimentation protocols commonly use 100-200 mcg/day subcutaneously or intramuscularly in 10-20 day courses, sometimes repeated 2-4 times per year. Russian small observational reports have used 0.2 mg orally twice daily for 20-30 days. No standardized dosing exists outside the Khavinson institute literature, and no rigorous human PK or dose-response data is published in indexed Western journals.

Research-use framing only. SavePeptides sells nothing for human consumption. Doses above reflect reported research / self-experimentation ranges, not clinical recommendations.

Editorial perspective

Essentially all published Pinealon evidence originates with the Khavinson group at the St. Petersburg Institute of Bioregulation and Gerontology, which holds patents on the bioregulator-peptide class and commercializes them — a notable conflict of interest. The hypothesized mechanism (direct binding of a 3-residue peptide to gene promoters) is biophysically unusual and has not been independently replicated. Treat all efficacy claims with skepticism and prefer to use Pinealon as a hypothesis-generating compound rather than a validated therapeutic.

— SavePeptides editorial desk · last updated 2026-05-25

Cautions & contraindications

Before researching this compound, note:

  • not FDA-approved; no completed human efficacy trials registered on ClinicalTrials.gov
  • all positive efficacy claims rest on a single research group (Khavinson, St. Petersburg) with commercial interest in the bioregulator class — limited independent replication
  • approximately half of source publications are Russian-language only and not peer-reviewed by Western standards
  • no rigorous human pharmacokinetic data published
  • pregnancy and lactation safety entirely unknown
  • research-chemical supply chain — purity, identity, and endotoxin testing vary widely
  • long-term safety not characterized
  • interactions with conventional cognitive medications not studied

Facts verified

2026-05-25

Confidence

low

What this means

  • evidence base is primarily Russian-language / Khavinson institute
  • no independent replication of efficacy claims
  • no completed human trials on ClinicalTrials.gov

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