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Noopept

Aliases: GVS-111 · N-fenilacetil-L-prolilglicin etil ester

Last verified: 2026-09-23

Approved drugLimited evidencePeptidesMedium interest

The short version

A dipeptide nootropic (prodrug of cycloprolylglycine) — approved in Russia for cognitive disorders. Anxiolytic and neuroprotective, structurally a "peptide piracetam". Key fact: Russian trials for mild cognitive impairment and post-TBI; scarce Western research.

Identity & type

Molecular type
peptide
Origin
A dipeptide nootropic (prodrug of cycloprolylglycine) — approved in Russia for cognitive disorders.

Mechanism of action

Metabolized to cycloprolylglycine → modulation of glutamatergic (AMPA) and cholinergic systems, increased BDNF/NGF, antioxidant.

not confirmed in humans

Dosing & routes

Official / clinical context

Approved drug — indications, dosing and warnings are defined by the official label. 10–30 mg/day orally (2×10 mg most common).

Regulator-approved labeling and published study designs — never a recommendation.

Community-reported practice

10–30 mg/day orally (2×10 mg most common). Mild but consistent effects: clearer focus, verbal fluency, reduced fog; some report headache and irritability at higher doses.

Unverified self-reports. Not medical advice. Not endorsement.

Expected effects (community)

Mild but consistent effects: clearer focus, verbal fluency, reduced fog; some report headache and irritability at higher doses.

Protocol — official vs community

Official / label

Approved in Russia (and some CIS markets) for mild cognitive impairment and post-traumatic brain injury sequelae: 10–30 mg/day orally, given as 10 mg 2–3× daily.

Duration: Russian label practice uses treatment courses of 1.5–3 months; some label schemes run 3 months on, then a month off.

A dipeptide prodrug of cycloprolylglycine. Western regulators have never reviewed it; the supporting trial base is predominantly Russian and low-visibility internationally.

Community (anecdotal)

10–30 mg/day oral, split into 2 doses; sublingual use of the same powder is common for perceived faster onset.

Cycle:
Many nootropic users follow the Russian course logic (8–12 weeks on); others take it daily for years.
Break:
1–4 weeks between courses for adherents of the course model.

One of the most-discussed Russian nootropics in Western communities. Reported effects are subtle and subjective; the structured course pattern comes from the Russian label, not from biohacker invention.

Human evidence

Russian trials for mild cognitive impairment and post-TBI; scarce Western research.

Preclinical evidence

The preclinical phase was completed and submitted to regulators as part of registration; pharmacology and toxicology details are part of the official label.

Known risks

  • Rare: headache, irritability, sleep disturbance if taken late.characterized

Teal: characterized in clinical/labeling contexts. Amber: theoretical or reported outside controlled settings.

Unknowns & evidence gaps

  • Long-term human safety
  • Optimal dose and pharmacokinetics

Frequently asked questions

References