COMPOUNDS / PEPTIDE / PINEALON
PEPTIDE

PINEALON

LOW RISK
BEST FOR:Neuroprotection●●●●●○○○○○5/10
PINEALON · GLU-ASP-ARG · GLUTAMYL-ASPARTYL-ARGININE · ПИНЕАЛОН · PINEALON PEPTIDE
PeptideNeuroprotectiveGeroprotectorRussianAntioxidantBioregulator

Synthetic tripeptide (Glu-Asp-Arg) with neuroprotective, antioxidant, and geroprotective properties developed in Russia.

ROUTE / DOSAGE
LOW100mcg
STANDARD100-200mcg
HIGH300mcg
Note: Typically 1-2 capsules daily; designed for oral bioavailability as a short peptide bioregulator
CYCLE
10-30 day course repeat after 3-6 months
BIOAVAILABILITY
Moderate oral (designed for oral activity as short peptide) high subq/im
ACTIVE DURATION
4-6h per dose (cumulative effects over course) (subjective)
STORAGE
Oral capsules: room temperature dry away from light. Injectable: refrigerate 2-8°C protect from freezing
HALF-LIFE
15-30min (plasma)
DURATION BREAKDOWN
Total10-30 days (course duration)
Onset1-3 days
Come up3-7 days
Peak2-4 weeks
Offset1-2 weeks post-course
After effectsweeks-months (sustained geroprotective effects reported)
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
6 documented
Neuroprotective against oxidative stress
Reduces reactive oxygen species accumulation
Improves cognitive function and spatial memory
Geroprotective and anti-aging effects
Reduces neuroinflammation under hypoxia
Modulates cell cycle and DNA gene expression
§ 02 — RISKS
No randomized controlled clinical trials exist; evidence is almost entirely preclinical
Prooxidant activity observed at certain doses in one human study
Long-term safety profile unknown
Limited pharmacokinetic and bioavailability data in humans
Potential inhibition of hematopoiesis noted in one small human study
§ 03 — INTERACTIONS
Interaction data not yet available for this compound.
§ 04 — SCIENCE

Pinealon was developed at the Saint-Petersburg Institute of Bioregulation and Gerontology by Khavinson and colleagues. In vitro studies demonstrate dose-dependent reduction of ROS in cerebellar granule cells, neutrophils, and PC12 cells, with accompanying decreases in necrotic cell death. Animal studies show improved cognitive function and spatial learning in offspring of rats with prenatal hyperhomocysteinemia, as well as neuroprotective effects under acute hypoxia and hypothermia in aged rats. A small human study (n=32) in patients with chronic polymorbidity and organic brain syndrome showed geroprotective and anabolic effects, though Vesugen outperformed Pinealon. Evidence is almost entirely preclinical with very limited human data; no randomized controlled trials exist.

§ 06 — SOURCES
[1]
PubMed PMID 41490200
pubmed.ncbi.nlm.nih.gov ↗
[2]
PubMed PMID 22567179
pubmed.ncbi.nlm.nih.gov ↗
[3]
PubMed PMID 21978084
pubmed.ncbi.nlm.nih.gov ↗
[4]
PubMed PMID 28509493
pubmed.ncbi.nlm.nih.gov ↗
[5]
PubMed PMID 25051764
pubmed.ncbi.nlm.nih.gov ↗
[6]
PubMed PMID 26390612
pubmed.ncbi.nlm.nih.gov ↗
[7]
PubMed PMID 22117547
pubmed.ncbi.nlm.nih.gov ↗
[8]
PubMed PMID 28539017
pubmed.ncbi.nlm.nih.gov ↗
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