Noopept
Omberacetam (N-phenylacetyl-L-prolylglycine ethyl ester, GVS-111)
Small dipeptide-derivative nootropic developed in Russia by JSC LEKKO in 1996. Marketed in Russia, Belarus, Ukraine, and several CIS states as a prescription cognitive enhancer for mild cognitive impairment, post-concussion syndrome, and asthenia. In the US it sits in a regulatory gray zone: FDA-classified as an unapproved drug analog of piracetam, but widely sold as a 'dietary supplement' or 'research chemical' online. Hungary scheduled it as a controlled psychoactive substance in 2020.
At a glance
- Half-life
- ~30 min Parent Noopept t½ ~30 min in plasma. Active metabolite cycloprolylglycine has a longer functional duration (~3-4 h) and is responsible for sustained subjective effects. Effective duration of action 4-6 h per dose.
- Routes
- Oral · Sublingual
- Vial sizes
- 10 mg · 20 mg
- Evidence base
- 3 studies 2 human · 1 review
Mechanism
Prodrug: rapidly metabolized to the active metabolite cycloprolylglycine (CPG), an endogenous dipeptide. CPG appears to act on AMPA / NMDA glutamate receptor subunits (positive modulation), upregulate BDNF and NGF expression, activate HIF-1α, and provide anti-oxidant + anti-glutamate-excitotoxicity protection. Structurally NOT a classic racetam despite being marketed alongside them. Better anxiolytic and autonomic effect vs piracetam in MCI. In a post-stroke MCI trial (20 mg/day for 8 weeks), cognitive improvement was reported.
Dosing
Any amounts shown here are reported from published studies only. 2 of 3 catalogued studies involved human subjects. COMPOUND does not publish its own dosing guidance.
Where a study reports an amount, it appears in that study's entry below, attributed to the source.
Published evidence
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Human RCT 2009
Comparative studies of Noopept and piracetam in the treatment of patients with mild cognitive disorders
Russian comparative trial: Noopept 20 mg/day vs piracetam 1200 mg/day in mild cognitive impairment. Both improved cognition; Noopept showed better anxiolytic + autonomic effect.
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Human observational 2011
Noopept in the treatment of mild cognitive impairment in patients with stroke
Open-label Russian clinical study: Noopept 20 mg/day x 8 weeks improved cognitive scores and reduced anxiety in post-stroke MCI patients.
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Review 2008
The original novel nootropic and neuroprotective agent noopept
Comprehensive review by the developing lab: mechanism, PK, preclinical and clinical findings.
Reported side effects
- Headache
- Occasional Mild · Often dose-related. Choline supplementation (alpha-GPC, CDP-choline) may reduce.
- Irritability / restlessness
- Occasional Mild · Reported with higher doses (>30 mg/day) or chronic use.
- Insomnia
- Occasional Mild
- Mild blood pressure elevation
- Rare Mild · Per Russian PI: caution in uncontrolled hypertension.
- Allergic skin reaction
- Rare Moderate · Per Russian PI.
Interactions
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Caffeine Synergy
Subjective synergy with caffeine + L-theanine. No formal PK study.
Storage
Tablets / powder stable at room temp, protect from moisture and light. Shelf-life 3 years.