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Omberacetam (Noopept)

Synthetic Dipeptide | Cognitive Enhancement Nootropic

Emerging Research
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What is Omberacetam (Noopept)?

Omberacetam (also called Noopept) is a small synthetic dipeptide-like compound studied in the nootropic research literature for its effects on memory and learning pathways, at doses reported to be far smaller than older compounds in its class. Once absorbed, it's converted into an active byproduct that researchers study for its influence on glutamate signaling and BDNF levels. It's sold here strictly as a research chemical for laboratory study, not for use in people or animals.

Key terms:

Omberacetam (Noopept) is a synthetic dipeptide.

Omberacetam (also called Noopept or GVS-111) is a lab-made two-amino-acid compound, N-phenylacetyl-L-prolylglycine ethyl ester. It was developed in Russia in 1996 and studied for strong effects on thinking and for neuroprotection (shielding nerve cells from damage). Its structure differs from the racetams, but it is grouped with them as a nootropic. It is a prodrug: the body converts it into an active byproduct called cycloprolylglycine (CPG). Research suggests it may support memory, learning, and neuroplasticity by increasing BDNF and NGF (nerve-growth signals) and by adjusting glutamate signaling — at doses 1,000 times lower than piracetam.

Key research areas

  • Primary administration route with rapid oral bioavailability
  • Convenient dosing with peak absorption within 7 minutes
  • Well-studied in clinical trials
  • Enhances memory consolidation and retrieval
  • Supports neuroplasticity through BDNF/NGF upregulation
  • Effective at doses 1000x lower than piracetam

Researched dosing

This table shows how researchers have structured study dosing schedules for Omberacetam — published research methodology and dose ranges, not personal usage instructions.

PhaseDoseFrequencyRoute
Cognitive studies (lower dose)10mg1-2 times dailyOral (sublingual or swallowed)
Standard cognitive studies10-20mg2-3 times dailyOral, taken with or without food
Higher-dose cognitive studies20-30mg2-3 times dailyOral, cycled 4-8 weeks
Cognitive-recovery studies20mgTwice dailyOral (as studied in clinical trials)
Lower-dose tolerability studies5-10mgOnce dailySublingual for enhanced absorption

Commonly cycled 8 weeks on, 2+ weeks off.

How it works

At the cell level, Omberacetam research looks at how its active byproduct (cycloprolylglycine) interacts with glutamate receptors and cholinergic signaling — the proposed basis for the memory- and learning-related effects reported in the literature.

Rapidly absorbed orally and converted to active metabolite cycloprolylglycine (CPG) which modulates AMPA/NMDA glutamate receptors and enhances cholinergic neurotransmission

Research applications

This section lists the body systems and research areas scientists have studied for Omberacetam — largely memory, learning, and neuroprotection research — a summary of what's been investigated in the literature, not medical claims about people.

Cognitive

Most studied

Improved memory consolidation and retrieval through enhanced synaptic plasticity and neurotrophic factor expression. Faster acquisition of new information via AMPA receptor modulation and enhanced long-term potentiation. Sustained attention improvements through acetylcholine sensitization and glutamatergic enhancement.

Neuroprotective

Well studied

Demonstrates significant neuroprotective effects against Alzheimer's disease-related pathology, attenuating apoptosis and reducing tau hyperphosphorylation in human neuronal cells exposed to amyloid-beta toxicity.

Neuroplasticity

Early research

Elevates BDNF and NGF mRNA levels in the hippocampus, supporting synaptic plasticity and long-term neuroplasticity benefits.

Dosage reference

Doses used in research
10–20 mg per dose
Frequency in studies
1-3 times daily, morning and early afternoon preferred
Handling
Reconstituted solution — research use only; not for administration
Timeline reported in studies
Onset 20-60 minutes, peak 2 hours, duration 3-5 hours
Storage
Room temperature, protect from moisture and light
Cycle length
4-8 weeks continuous use recommended
Break between cycles
2-4 weeks break between cycles to prevent tolerance

Interactions

This list shows which other nootropic-research compounds scientists study alongside Omberacetam, and notes that a dietary choline source is often included in study designs to offset a commonly reported research finding (mild headache).

Semax — synergistic Selank — synergistic NA-Semax-Amidate — compatible Cerebrolysin — compatible Dihexa — compatible Choline Sources — synergistic

Reconstitution & storage

Omberacetam is typically studied as tablets, capsules, or a measured powder rather than an injectable, so this section covers precise measurement and choline-pairing notes instead of a mixing procedure.

  1. Omberacetam is typically supplied as tablets (10mg), capsules, or powder form
  2. For powder: Use precision scale capable of measuring milligrams accurately
  3. Consider pairing with a choline source (Alpha-GPC 300mg or CDP-Choline 250mg) to prevent headaches
  4. Store the reconstituted solution refrigerated (2–8°C), labeled with the date and concentration, for laboratory research use only.

Lyophilized: Room temperature, use within Not specified

Reconstituted: 2-6°C, use within Not specified

Quality indicators

These are the visual and lab-report checks researchers use to confirm an Omberacetam sample is pure and correctly identified before it goes into a study.

White crystalline powder - Omberacetam should be white to off-white crystalline powder without discoloration

Third-party testing - Certificate of analysis showing purity ≥98% with HPLC verification

Proper packaging - Sealed containers protected from moisture with desiccant packets

Accurate dosing - Tablets/capsules should contain stated amount (typically 10mg per unit)

Headache potential - May cause headaches if taken without adequate choline - supplement accordingly

Discoloration or clumping - Yellow discoloration or excessive clumping may indicate degradation or contamination

What to expect

This timeline summarizes what research literature reports at each stage of a study — research context for comparing studies, not a personal-results promise.

Days 1-3

Subtle cognitive clarity and mild focus enhancement; possible initial headache if not using choline

Week 1

Noticeable improvement in memory recall and verbal fluency; adjust dosing as needed

Week 2-3

Enhanced learning capacity and sustained attention; mood stabilization effects may emerge

Week 4-6

Peak cognitive benefits with improved stress resilience and mental stamina

Week 6-8

Sustained effects; consider cycle break to maintain sensitivity

Safety notes

This section covers handling cautions and regulatory notes for Omberacetam in a laboratory setting — research-use-only scope and interaction flags drawn from the literature, not medical safety advice for people.

  • Start with 10mg once daily to assess individual response before increasing dose
  • Always pair with a choline source (Alpha-GPC or CDP-Choline) to prevent headaches
  • Avoid evening dosing as cognitive stimulation may interfere with sleep
  • Do not combine with other strong cholinergic or glutamatergic compounds without caution
  • Not recommended for pregnant or breastfeeding women due to lack of safety data
  • Individuals with liver conditions should consult healthcare provider before use

Regulatory status

  • Not approved by the FDA for any indication.
  • Supplied and described for laboratory research use only — not for human or veterinary use.

Community data

Community Poll

How would you rate your overall experience with this peptide?

1284 votes · Community data

Community Insights

82%reported positive results
68%noticed effects within 2 weeks
91%would recommend to others

Based on data the community reported. Not clinical proof.

References

  1. In vitro · Multiple concentrations · Not specified

    Omberacetam demonstrated significant neuroprotective effects against Alzheimer's disease-related pathology, attenuating apoptosis and reducing tau hyperphosphorylation in human neuronal cells exposed to amyloid-beta toxicity.

  2. Rat · 0.5mg/kg IP · Single dose

    Acute administration elevated BDNF mRNA levels by up to 1.4-fold and NGF mRNA by 1.3-fold in hippocampus within 3 hours post-injection, demonstrating rapid neurotrophic activity supporting neuroplasticity.

  3. Human · 20mg daily vs Piracetam 1200mg · 56 days

    Patients with cognitive impairment from vascular cerebral damage or post-traumatic injury showed universal improvement on measured parameters. MMSE scores increased from 26 to 29 in the Omberacetam group with 1.8-fold fewer side effects compared to piracetam.