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    Noopept molecular structure

    Noopept Stats & Data

    gvs-111 omberacetam sgs-111
    NPS DataHub
    MW318.37
    FormulaC17H22N2O4
    CAS157115-85-0
    IUPACEthyl 1-(phenylacetyl)-L-prolylglycinate
    SMILESCCOC(=O)CNC(=O)C1CCCN1C(=O)Cc1ccccc1
    InChIKeyPJNSMUBMSNAEEN-AWEZNQCLSA-N
    Others
    Half-Life Likely short for parent compound (often cited ~0.5 hour); human PK data are sparse and effects outlast plasma levels, suggesting active metabolites.

    Receptor Profile

    Receptor Actions

    Modulators
    AMPA receptor positive allosteric modulator
    Acetylcholine modulator
    Other
    Prodrug (metabolizes to cycloprolylglycine)

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Likely short for parent compound (often cited ~0.5 hour); human PK data are sparse and effects outlast plasma levels, suggesting active metabolites.
    Addiction Potential
    Low; not considered classically addictive. Some users report psychological reliance with daily use and cognitive 'dullness' on cessation; formal dependence data in healthy users are lacking.

    Tolerance Decay

    Full tolerance 0h Half tolerance 7d Baseline ~14d

    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

    Piracetam
    20% ●○○
    Aniracetam
    20% ●○○

    Experience Report Analysis

    Erowid
    13 Reports
    2012–2023 Date Range
    12 With Age Data
    10 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 13 experience reports (13 Erowid)

    13 Reports
    10 Effects Detected
    7 Positive
    3 Adverse
    0 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 7

    Stimulation 53.8% 70%
    Focus Enhancement 38.5% 70%
    Empathy 30.8% 70%
    Music Enhancement 23.1% 70%
    Color Enhancement 23.1% 70%
    Euphoria 23.1% 70%
    Introspection 23.1% 70%

    Adverse Effects 3

    Anxiety 69.2% 70%
    Confusion 23.1% 70%
    Memory Suppression 23.1% 70%

    Real-World Dose Distribution

    62K Doses

    From 22 individual dose entries

    Oral (n=11)

    Median: 20.0mg 25th: 10.0mg 75th: 27.5mg 90th: 30.0mg
    mg/kg median: 0.308 mg/kg 75th: 0.401

    Form / Preparation

    Most common forms and preparations reported

    Redose Patterns

    Redosing behavior across 10 reports

    20.0% Redosed
    1.3 Avg Doses

    Harm Reduction

    drugs.wiki

    Potency 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.

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