Noopept Stats & Data
CCOC(=O)CNC(=O)C1CCCN1C(=O)Cc1ccccc1PJNSMUBMSNAEEN-AWEZNQCLSA-NReceptor Profile
Receptor Actions
Tolerance & Pharmacokinetics
drugs.wikiTolerance Decay
Many report subtle tolerance after continuous daily use for weeks; limited to anecdotal evidence. Spacing doses (e.g., 2–3 days/week) or cycling may help maintain effect. Cross-tolerance within racetams is plausible but not quantified.
Cross-Tolerances
Experience Report Analysis
ErowidDemographics
Gender Distribution
Age Distribution
Reports Over Time
Effect Analysis
ErowidEffects aggregated from 13 experience reports (13 Erowid)
Effect Sentiment Distribution
Confidence Distribution
Positive Effects 7
Adverse Effects 3
Real-World Dose Distribution
62K DosesFrom 22 individual dose entries
Oral (n=11)
Form / Preparation
Most common forms and preparations reported
Redose Patterns
Redosing behavior across 10 reports
Harm Reduction
drugs.wikiPotency varies by supplier; unregulated market products have shown high rates of mislabeling in drug-checking programs for other substances—obtain third-party COAs and consider reagent or service-based testing when available. Start with 3–5 mg to assess sensitivity and avoid redosing within the first 2 hours to reduce risk of headaches, irritability, or insomnia. Insomnia is more likely with late-day dosing; avoid taking after mid-afternoon until you understand your response. Headaches are reported and often ascribed by users to cholinergic imbalance; while some find choline supplements helpful, controlled evidence is limited—add only if a consistent personal benefit is observed and keep doses modest. Combination with alcohol has produced unpleasant and risky experiences for some (confusion, dysphoria); if mixing, use minimal alcohol and avoid escalating either substance. Co-administration with phenibut or other CNS depressants can unpredictably blunt or intensify effects—space uses by at least 12–24 hours and avoid first-time combinations. Intranasal use is not recommended due to local irritation and uncertain bioavailability; oral or sublingual routes are safer and sufficient. If using daily, consider cycling (e.g., several weeks on followed by a similar or longer break) to limit tolerance and evaluate ongoing need; data are anecdotal and long-term safety is not established. Avoid in pregnancy/breastfeeding and in individuals with uncontrolled anxiety or sleep disorders until a cautious single low-dose trial in a safe setting demonstrates tolerability. Do not drive or operate machinery on first use or after dose changes, given interindividual variability and occasional paradoxical anxiety or sedation.
References
Data Sources
Cited References
- Bluelight: Noopept Megathread
- Drug Users Bible: Noopept
- DrugBank: Omberacetam
- Erowid: Noopept Vault
- Examine.com: N-Phenylacetyl-L-prolylglycine ethyl ester
- Gudasheva et al. 2002 - The original novel nootropic and neuroprotective agent noopept
- IJEST 2021 - Finding the optimal dosage for nootropic agent Noopept
- Neznamov & Teleshova 2009 - Comparative studies of Noopept and piracetam
- Ostrovskaya et al. 2018 - Pharmacokinetics of noopept and its active metabolite cycloprolyl glycine in rats
- PsychonautWiki: Omberacetam
- PubChem: 1-(2-Phenylacetyl)-L-prolylglycine ethyl ester
Drugs.wiki References
- DrugBank: Avotermin (DB11955) shows user-provided ID is a different drug
- Drug Users Bible: Noopept (dosage ranges, context)
- Erowid Experience Vaults (Noopept entries incl. with alcohol/phenibut)
- BlueLight: Noopept & The Placebo Effect (community trial write-up)
- SubstanceSearch: Noopept (onset/duration overview)
- Effect Index: Memory enhancement / thought-organization (lists Noopept among inducers)