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COGNITIVEPEPTIDE PROFILE

Noopept

Also known as GVS-111, Omberacetam, N-phenylacetyl-L-prolylglycine ethyl ester

Noopept (INN: Omberacetam) is a synthetic dipeptide derivative developed in Russia by the Zakusov Research Institute of Pharmacology. Its chemical structure is N-phenylacetyl-L-prolyl-glycine ethyl ester, representing the ethyl ester prodrug of the endogenous cycloprolylglycine (CPG) dipeptide. Effective at doses approximately 1000-fold lower than piracetam by weight, it is among the most potent studied nootropic compounds. It was developed for cognitive impairment associated with aging, vascular disorders, and traumatic brain injury.

Last updated June 25, 2026

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Noopept: quick citable summary

Noopept is listed by PeptaHub as a cognitive peptide with a research only legal-status classification. The page summarizes mechanism, research context, common routes, safety notes, and references for writers and AI answer engines.

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PeptaHub. “Noopept: Mechanism, Research Context, Safety.” peptahub.com, 2026. https://peptahub.com/peptides/noopept. Licensed CC BY 4.0.

License: Creative Commons Attribution 4.0 International. Link back to https://peptahub.com/peptides/noopept.

SAMEAS / EXTERNAL IDS
Noopept CAS: 157115-85-0
QUICK ANSWER

What is Noopept?

Noopept (Omberacetam) is a synthetic dipeptide derivative roughly 1000-fold more potent than piracetam. It acts via AMPA receptor modulation and BDNF/NGF upregulation, registered as a prescription drug in Russia though no FDA-regulated trials exist.

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Overview

Noopept (INN: Omberacetam) is a synthetic dipeptide derivative developed in Russia by the Zakusov Research Institute of Pharmacology. Its chemical structure is N-phenylacetyl-L-prolyl-glycine ethyl ester, representing the ethyl ester prodrug of the endogenous cycloprolylglycine (CPG) dipeptide. Effective at doses approximately 1000-fold lower than piracetam by weight, it is among the most potent studied nootropic compounds. It was developed for cognitive impairment associated with aging, vascular disorders, and traumatic brain injury.

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Mechanism of action

After oral absorption, Noopept is hydrolyzed to its active metabolite cycloprolylglycine (CPG), which modulates AMPA-type glutamate receptors and facilitates long-term potentiation in hippocampal circuits. Noopept also increases cerebral NGF (nerve growth factor) and BDNF expression, supporting neuronal survival and synaptic density. Additional mechanisms include modulation of voltage-dependent calcium channels and calcium-activated potassium channels, regulating neuronal excitability. Research has identified HIF-1 (hypoxia-inducible factor-1) DNA-binding activity as another proposed primary mechanism, potentially providing neuroprotection under hypoxic or ischemic conditions. Antioxidant activity via inhibition of intracellular reactive oxygen species accumulation contributes to its neuroprotective profile.

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Reported study ranges

PurposeRouteReported rangeFrequency
cognitive enhancement researchoral1030 mgtwice daily

Reported ranges are for research context only. Consult a qualified healthcare professional before using any peptide.

Convert Noopept research-range units

Need to convert mg to mcg, dose volume, or U-100 syringe units? The Noopept dose calculator is preloaded with these ranges, or use the general dose unit converter.

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Research summary

Russian preclinical studies across multiple animal models document cognitive enhancement, reduced anxiety, and neuroprotection against ischemia, oxidative stress, and amyloid toxicity. In cultured human cortical neurons from normal and Down syndrome tissue, GVS-111 protected against hydrogen peroxide damage with an IC50 of 1.21 microM and outperformed piracetam, vitamin E and other antioxidants (Int J Dev Neurosci 2003) — a cell culture result, not a clinical one. The compound retains nootropic activity after oral administration in rats. On the human side, Neznamov and Teleshova compared Noopept against piracetam in patients with mild cognitive disorders from vascular or traumatic brain disease and reported comparable or better results for Noopept; the study was not placebo-controlled. No FDA-regulated clinical trial has been completed as of 2026.[1][2][3][4][5][6]

📄This section cites 6 peer-reviewed sources. View all references →
§ 04b

Evidence grading

Each claimed benefit is graded by the strength of available evidence. Grades reflect study quality, not effect size.

preliminary
Enhances memory/cognitionNeznamov Neurosci Behav Physiol 2009: Russian comparative study against piracetam in patients with mild cognitive disorders from vascular or traumatic brain disease. Not placebo-controlled and not replicated under ICH-GCP conditions
preliminary
Upregulates NGF and BDNFOstrovskaya Bull Exp Biol Med 2008: rat hippocampus. Rodent finding, no human data
preliminary
Neuroprotection against oxidative stressPelsman Int J Dev Neurosci 2003: cultured human cortical neurons, normal and Down syndrome, IC50 1.21 microM against H2O2 damage. Cell culture only
preliminary
Attenuates tau hyperphosphorylation2014 J Biomed Sci AD cellular model showed apoptosis and tau reduction in vitro

Strong = multiple RCTs · Moderate = limited trials or observational · Preliminary = animal or in vitro only · Insufficient = anecdotal or no published data

§ 05

Side effects

Headache (common, especially without choline supplementation)
Irritability at high doses
Brain fog or fatigue
Sleep disturbance if dosed late
Rare: nausea

Side effects vary by individual. This is not an exhaustive list. Report unusual symptoms to a healthcare professional.

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Common stacks

Peptides commonly paired with Noopept for synergistic effects.

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Sourcing & access

Research compound

Noopept is classified as a research compound. Regulatory status varies by jurisdiction. Always verify current legal status and source from vendors providing third-party certificates of analysis (COA).

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Frequently asked questions

Noopept (Omberacetam, GVS-111) is a synthetic dipeptide derivative developed in Russia as a prodrug of cycloprolylglycine. It is one of the most potent studied nootropics, effective at doses approximately 1000-fold lower than piracetam by weight.

After oral absorption, Noopept is hydrolyzed to cycloprolylglycine (CPG), which modulates AMPA glutamate receptors and facilitates long-term potentiation in hippocampal circuits. It also increases NGF and BDNF expression, modulates calcium and potassium channels, and activates HIF-1 DNA-binding for neuroprotection under hypoxic conditions.

Common side effects include headache (especially without choline supplementation), irritability at high doses, brain fog or fatigue, and sleep disturbance if dosed late. It is a registered prescription drug in Russia but is not FDA-approved; it is unscheduled in the UK and many other jurisdictions.

The Russian registered dose is 10 mg twice daily for a course of 1.5 to 3 months, and that is also the dose used in the comparative study against piracetam. Higher intakes and the sublingual or intranasal routes circulate in user reports but are not supported by the label or by a trial.

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Research references

  1. Neuroprotective properties of nootropic dipeptide GVS-111 in in vitro oxygen-glucose deprivation, glutamate toxicity and oxidative stressAndreeva NA, Stel'mashuk EV, Isaev NK, et al.Bull Exp Biol Med, 2000PubMed
  2. Noopept stimulates the expression of NGF and BDNF in rat hippocampusOstrovskaya RU, Gudasheva TA, Zaplina AP, et al.Bull Exp Biol Med, 2008PubMed
  3. Neuroprotective effect of novel cognitive enhancer noopept on AD-related cellular model involves the attenuation of apoptosis and tau hyperphosphorylationOstrovskaya RU, Vakhitova YV, Kuzmina USh, et al.J Biomed Sci, 2014PubMed
  4. Proline-containing dipeptide GVS-111 retains nootropic activity after oral administrationOstrovskaya RU, Mirsoev TK, Romanova GA, et al.Bull Exp Biol Med, 2001PubMed
  5. GVS-111 prevents oxidative damage and apoptosis in normal and Down's syndrome human cortical neuronsPelsman A, Hoyo-Vadillo C, Gudasheva TA, et al.Int J Dev Neurosci, 2003PubMed
  6. Comparative studies of Noopept and piracetam in the treatment of patients with mild cognitive disorders in organic brain diseases of vascular and traumatic originNeznamov GG, Teleshova ESNeurosci Behav Physiol, 2009PubMed
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