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Noopept

Omberacetam; GVS-111; N-phenylacetyl-L-prolylglycine ethyl ester

2 min read · Updated July 27, 2026 · 6 references

Curated by PeptideInfo Wikilast reviewed how we verify

In brief · TL;DR
Limited/early human data — not approved

Noopept is a synthetic prolylglycine-derived small molecule with limited, mostly Russian-language clinical literature and a larger preclinical literature; robust human efficacy and safety are not established.

Evidence: Only small/early human studies; not approved.

  • Small and open human studies provide low-certainty evidence
  • Animal mechanisms do not establish clinical cognitive benefit
  • No FDA/EMA-approved regimen is asserted
↓ Read the full referenced entry below

Noopept is a synthetic prolylglycine-derived small molecule with limited, mostly Russian-language clinical literature and a larger preclinical literature; robust human efficacy and safety are not established.

Overview

Noopept, also called omberacetam or GVS-111, is a synthetic prolylglycine derivative. It is often called a peptide or dipeptide, but PubChem classifies a defined small molecule. The evidence base combines animal work with a few small or open clinical reports, mostly published in Russian.

Low-certainty human evidence

Published human signals are not equivalent to replicated randomized evidence, and they do not establish broad cognitive enhancement.

Identity and chemistry

PropertyVerified value
PubChem CID180496
Molecular formulaC17H22N2O4
Molecular weight318.4 g/mol
CAS number157115-85-0

The chemical name is N-phenylacetyl-L-prolylglycine ethyl ester. This identity distinguishes the molecule from endogenous peptides and from unrelated products sold under nootropic labels.

Proposed mechanisms

Rat studies reported changes in hippocampal NGF and BDNF messenger RNA after administration. Mouse and cell models have examined memory, amyloid-related endpoints, oxidative stress and cholinergic effects. These are mechanistic hypotheses from models; they do not establish the mechanism or magnitude of effect in humans.

Human evidence

A 2008 Russian-language clinical report described EEG changes in patients with cognitive symptoms of vascular or post-traumatic origin. A later open prospective report enrolled 60 post-stroke patients and reported improved cognitive-test results after two months relative to controls. The abstract describes an open design, limited reporting and surrogate outcomes. These limitations make the findings preliminary and difficult to generalise.

Evidence-integrity note

A 2021 PubMed record concerning Noopept’s antioxidant effects is marked retracted. It is retained in the references solely as an integrity warning and is not used to support efficacy or mechanism. Retraction screening matters because citation count alone can otherwise exaggerate the evidence base.

Clinical and regulatory context

This review does not establish an FDA or EMA marketing authorisation. Regional availability or historical use cannot be translated into global approval, and the cited human papers do not provide the evidence package expected for a modern broad indication.

Safety and dosing

Long-term human safety, interaction risk and adverse-event incidence remain insufficiently characterised in the reviewed sources. One open study used 20 mg daily for two months, but that is a study method, not a regulator-approved or general regimen.

No established dose

The page intentionally does not convert exploratory study exposure into self-use guidance.

Evidence conclusion

Noopept has more than purely animal evidence, but the human layer is small, open and incompletely reported. Better controlled, independently replicated trials with transparent safety reporting are needed before clinical cognitive claims can be considered reliable.

References

  1. 1.
    PubChem Compound Summary: Noopept (CID 180496) source
  2. 2.
    Clinical and EEG study in cognitive impairment source
  3. 3.
    Open prospective post-stroke study source
  4. 4.
    Rat hippocampal NGF and BDNF expression study source
  5. 5.
    Mouse olfactory-bulbectomy model source
  6. 6.
    Retracted Noopept article record source

Frequently asked questions

What is Noopept?
Noopept is a synthetic prolylglycine-derived small molecule with limited, mostly Russian-language clinical literature and a larger preclinical literature; robust human efficacy and safety are not established.
Is Noopept approved as a medicine, and where?
No. Noopept is not an approved medicine anywhere. It is handled as a research chemical, with only limited or early-stage human data.
What is Noopept studied for?
Noopept is most often discussed in the context of cognition, mood & sleep. Being studied for an area does not mean it is proven or approved for it.
Does Noopept have human clinical trials?
Only to a limited extent. A small number of early-stage human studies exist, but the evidence is preliminary and Noopept is not approved.

Educational disclaimer. This article summarizes published research for informational purposes and is not medical advice. Noopept is a research chemical not approved for human use. Consult a qualified healthcare professional before making health decisions.

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