Pinealon

Peptideoral · inferred

Synthetic tripeptide (Glu-Asp-Arg / EDR) developed by the Khavinson group. Brain-penetrant peptide that modulates gene expression in CNS tissues. No published formal pharmacokinetic studies; as an ultrashort tripeptide, plasma half-life is estimated at minutes. Studied for neuroprotection against oxidative stress and cognitive decline.

Projected serum levels — 1 mg, once daily

Pinealon
Pinealon modeled serum levels, 1 mg once daily over 15 days Population-based pharmacokinetic estimate. Steady state reached after approximately 1 days. 0 0.25 0.50 0.75 1 Day 0 Day 4 Day 8 Day 11 Day 15 Time on a regular schedule ≈ steady state · day 1
Pinealon modeled serum levels with a loading dose of 1.3 mg, then 1 mg once daily The first dose is larger so levels approach steady state faster. 0 0.25 0.50 0.75 1 Day 0 Day 4 Day 8 Day 11 Day 15 Time on a regular schedule

Maintenance schedule: 1 mg once daily (oral).

Loading schedule: 1.3 mg on day 1, then 1 mg once daily — reaching therapeutic levels sooner.

Modeled steady state after ~1 days: peak ≈ 0.019 mg, trough ≈ 0.000 mg body load. Population-based estimate over 15 days for a 1 mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.

Key facts

Category
Peptide
Route modeled
Oral
Model confidence
inferred
Half-life
7 min
Common dose
1 mg
Suggested maximum
10 mg/day
Reference dose range
0.50–10 mg (single dose)
Suggested cadence
once daily

Research behind this entry

  1. Pinealon increases cell viability by suppression of free radical levels and activating proliferative processes Khavinson VK et al. · Rejuvenation Research, 2011 DOI

    Demonstrated Pinealon (EDR) increases cell viability by suppressing reactive oxygen species and activating proliferative processes in neuronal cell cultures under oxidative stress.

  2. Pinealon protects the rat offspring from prenatal hyperhomocysteinemia Khavinson VK et al. · International Journal of Clinical and Experimental Medicine, 2011 DOI

    Showed prenatal Pinealon administration protected offspring from hyperhomocysteinemia-induced neurodevelopmental damage, improving cognitive function and cerebellar neuron resistance to oxidative stress.

2 published studies referenced in the app, each with a plain-language summary.