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    Phenylpiracetam: Complete Research Guide to Fonturacetam

    A practical review of phenylpiracetam, a phenylated racetam with stimulant-like properties, limited Western clinical evidence, and explicit WADA prohibition as fonturacetam.

    Cognition
    Psychostimulant
    Physical Performance
    Medically reviewed byICL Medical TeamLast reviewed 23 May 2026Medical disclaimer

    Overview

    Phenylpiracetam, also called fonturacetam or carphedon, is a phenylated derivative of piracetam developed in the Soviet/Russian nootropic tradition. The added phenyl group changes potency and produces a more stimulant-like profile than classic piracetam. It is used in some countries as Phenotropil, but it is not FDA-approved in the United States.

    Mechanistically, phenylpiracetam is not fully mapped. Animal and pharmacology studies suggest effects on operant behavior, fatigue resistance, memory models, and possibly dopamine transporter-related activity for specific stereoisomers. The practical user experience often includes alertness, drive, cold tolerance, and reduced fatigue, but the human evidence base is not robust by modern standards.

    Phenylpiracetam is prohibited in sport by the World Anti-Doping Agency under the name fonturacetam. That matters for competitive athletes even when use is outside competition, because anti-doping rules can be strict and product contamination is common in the nootropic market. It should not be treated as a benign cognitive vitamin.

    This guide explains what is known, what is extrapolated, and what should stay cautious: stimulant-like side effects, tolerance, sleep disruption, anxiety, blood pressure concerns, sourcing risk, and the difference between Russian clinical use and FDA-reviewed approval.

    Quick facts

    Mechanism
    Phenylated racetam with stimulant-like nootropic activity
    Primary use
    Cognition and fatigue research
    Evidence
    limited
    FDA
    Not approved
    Route
    Oral capsules or tablets
    Typical results
    Acute stimulation and alertness with tolerance risk

    Chemical information

    Molecular mass
    218.26 g/mol
    Chemical formula
    C₁₂H₁₄N₂O₂

    Phenylpiracetam has molecular mass 218.26 g/mol and formula C12H14N2O2. It is a small racetam derivative, not a peptide, with a phenyl group attached to the piracetam scaffold.

    How Phenylpiracetam works

    Phenylpiracetam appears to combine racetam-like neuromodulatory effects with a stimulant-like behavioral profile. The phenyl substitution likely improves blood-brain barrier penetration compared with piracetam and may change interaction with monoamine systems. Evidence for precise receptor binding remains incomplete, so user-facing claims should stay conservative: alertness and fatigue resistance are more defensible than broad intelligence enhancement.

    Early Russian preclinical work reported stronger central neurotropic effects than piracetam, including activation of operant behavior and effects in amnesia and vestibular models. Later work on R-phenylpiracetam stereoisomers has explored dopamine transporter inhibition and anti-inflammatory or neuroprotective effects in animal models. These findings are interesting but do not define an approved clinical protocol.

    Compared with classic racetams, phenylpiracetam is more likely to feel stimulating. That can be useful in fatigue research but can also cause insomnia, irritability, anxiety, appetite suppression, and blood pressure concerns. Tolerance is a common user report, though formal tolerance studies are limited.

    The regulatory and sports context is unusually important. WADA lists fonturacetam as a prohibited stimulant. For athletes, even small exposures from mislabeled products can create consequences. For non-athletes, the same fact signals that phenylpiracetam has meaningful stimulant pharmacology and should not be stacked casually with other stimulants.

    • Phenylated racetam: Structural modification increases CNS activity compared with piracetam
    • Stimulant-like profile: Users may experience alertness, drive, and reduced fatigue
    • Monoamine uncertainty: Dopamine transporter findings exist but do not fully explain effects
    • WADA prohibition: Listed as fonturacetam under prohibited stimulants
    • Tolerance concern: Repeated use may rapidly reduce perceived benefit
    • Sleep impact: Late dosing can disrupt sleep and increase next-day fatigue

    Pharmacokinetics

    Published human PK information is limited and not comparable to FDA labels for approved stimulants. Claims about duration and dosing are often based on Russian product use or user reports rather than modern PK trials.

    ParameterValueSignificance
    RouteOralMost use involves capsules or tablets
    Half-lifeNot well established in open Western sourcesAvoid precise claims without formulation-specific data
    OnsetOften reported within hoursSubjective stimulation may guide unsafe redosing
    MetabolismLimited public human dataInteraction prediction is uncertain
    StereochemistryR- and S-isomers studiedIsomer-specific effects may differ from racemic products
    TestingRelevant to anti-dopingAthletes should avoid due to WADA listing

    Dosing & administration

    There is no FDA-approved phenylpiracetam dose. Russian clinical or product dosing practices should not be automatically applied to unregulated powders or imported capsules. Users should be especially cautious with product identity and stimulant stacking.

    Because tolerance and insomnia are common practical issues, daily use is hard to justify from the evidence base. Any research-style use should separate phenylpiracetam from caffeine, amphetamines, modafinil, yohimbine, or other stimulants until individual response is clear.

    Competitive athletes should avoid phenylpiracetam entirely unless an anti-doping professional has reviewed the situation. WADA lists fonturacetam explicitly, and no cognitive benefit is worth an avoidable anti-doping violation.

    Important: These dosing ranges are not FDA-approved. Any use should be under qualified medical supervision.

    Calculate dose & reconstitution

    Side effects & safety

    Phenylpiracetam has less severe dependence literature than phenibut, but its stimulant-like profile, uncertain long-term safety, and WADA status call for restraint. It is not FDA-approved and should not be used to push through illness, sleep deprivation, or cardiovascular symptoms.

    Common

    • Insomnia
    • Irritability
    • Headache
    • Anxiety or jitteriness
    • Reduced appetite
    • Dry mouth

    Serious / potential risks

    • Marked blood pressure or heart rate elevation in susceptible users
    • Panic or agitation when stacked with stimulants
    • Positive anti-doping test risk
    • Unknown long-term neuropsychiatric effects
    • Contamination or substitution from unregulated suppliers

    Drug interactions

    Interaction data are limited; risk assessment is based on stimulant-like effects and pharmacology.

    MedicationInteractionRecommendation
    Amphetamine or methylphenidateAdditive stimulation and cardiovascular strainAvoid unsupervised stacking
    Modafinil or armodafinilIncreased insomnia, anxiety, and overstimulationUse caution
    MAO inhibitorsTheoretical monoamine-related riskAvoid without physician guidance
    CaffeineMore jitteriness and sleep disruptionStart low or avoid combining
    AntihypertensivesStimulant effects may complicate blood pressure controlMonitor blood pressure

    Storage & handling

    Lyophilized (powder)

    • Store at -20°C to 4°C (freezer or refrigerator)
    • Protect from light and moisture
    • Stable for 12–24 months when stored properly
    • Keep in original sealed container until reconstitution

    Reconstituted solution

    • Refrigerate at 2–8°C after reconstitution
    • Use bacteriostatic water for multi-dose reconstitution
    • Typical stability: 14–28 days refrigerated
    • Do not freeze reconstituted solution

    Cost & availability

    SourceCostNotes
    Nootropic vendorsVariable capsule or powder pricingQuality and authenticity vary
    Imported productsMarket dependentRegulatory and customs status may vary
    Sports compliancePotential career costWADA-prohibited status is the main issue for athletes

    The bottom line

    Phenylpiracetam is best understood as a stimulant-leaning racetam with limited high-quality Western clinical data. It may improve alertness and fatigue in some users, but it is not FDA-approved, can disrupt sleep and anxiety, and is prohibited in sport as fonturacetam.

    Best for

    • Researchers studying racetam analogs
    • Short-term fatigue and vigilance research
    • Users who can monitor sleep and blood pressure
    • Non-athletes aware of stimulant risk

    Not for

    • Competitive athletes
    • People with uncontrolled hypertension
    • Anxiety-prone stimulant responders
    • Daily unsupervised cognitive enhancement

    Related compounds

    Frequently asked questions

    References

    1. [1] Bobkov IuG, Morozov IS, Glozman OM, Nerobkova LN, Zhmurenko LA. Pharmacological characteristics of a new phenyl analog of piracetam--4-phenylpiracetam. Biulleten Eksperimentalnoi Biologii i Meditsiny (1983). PMID: 6403074
    2. [2] Malykh AG, Sadaie MR. Piracetam and piracetam-like drugs: from basic science to novel clinical applications to CNS disorders. Drugs (2010). doi: 10.2165/11319230-000000000-00000 PMID: 20166767
    3. [3] Vavers E, Zvejniece L, Svalbe B, et al.. Neuroprotective and anti-inflammatory activity of DAT inhibitor R-phenylpiracetam in experimental models of inflammation in male mice. Inflammopharmacology (2020). doi: 10.1007/s10787-020-00705-7 PMID: 32279140
    4. [4] Thevis M, Sigmund G, Schiffer AK, Schanzer W. Determination of stimulants and narcotics in doping control analysis. Drug Testing and Analysis (2009).
    5. [5] World Anti-Doping Agency. The Prohibited List: International Standard. WADA (2025).
    6. [6] Gualtieri F, Manetti D, Romanelli MN, Ghelardini C. Design and study of piracetam-like nootropics, controversial members of the problematic class of cognition-enhancing drugs. Current Pharmaceutical Design (2002).