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    Adrafinil molecular structure

    Adrafinil Stats & Data

    Olmifon Crl 40028
    NPS DataHub
    MW289.36
    FormulaC15H15NO3S
    CAS63547-13-7
    IUPAC2-Benzhydrylsulfinyl-~{N}-hydroxyacetamide
    SMILESONC(=O)CS(=O)C(c1ccccc1)c1ccccc1
    InChIKeyCGNMLOKEMNBUAI-UHFFFAOYSA-N
    Psychoactive Class Stimulant

    Pharmacology

    DrugBank
    State Solid

    Description

    Adrafinil is a mild central nervous system stimulating drug typically employed to relieve excessive sleepiness and inattention in geriatric patients. It is also been used off-label to prevent fatigue or falling asleep for extended periods of time. Adrafinil does not currently have FDA approval and is thus unregulated in the United States. It was marketed in France and elsewhere in Europe under the trade name Olmifon until September 2011 when France's FDA equivalent reassessed the drug and withdrew marketing permission. Adrafinil is metabolized to modafinil.

    Pharmacodynamics

    Adrafinil is a prodrug; it is primarily metabolized in vivo to modafinil, resulting in nearly identical pharmacological effects. Unlike modafinil, the active metabolite must accumulate before the drug is able to act. Oral adrafinil without food usually begins to act within 45 minutes to 1 hour.

    Indication

    Used to relieve excessive sleepiness and inattention in elderly patients.

    Receptor Profile

    Receptor Actions

    Inhibitors
    Atypical dopamine reuptake inhibitor
    Other
    prodrug of modafinil

    History & Culture

    1974–1985

    Adrafinil was discovered in 1974 by two chemists working at the French pharmaceutical company Laboratoires Lafon. The compound emerged unexpectedly during a screening program aimed at identifying novel analgesic agents. Rather than demonstrating pain-relieving properties, pharmacological studies revealed that adrafinil produced psychostimulant-like effects in animals, including hyperactivity and sustained wakefulness. Two years after the initial discovery, in 1976, researchers identified modafinil as the primary active metabolite responsible for adrafinil's wakefulness-promoting effects. Modafinil demonstrated greater potency than its parent compound in animal studies and was subsequently selected for parallel clinical development alongside adrafinil. The first human trials of adrafinil were conducted between 1977 and 1978, specifically investigating its potential for treating narcolepsy. Alexander Shulgin published the first detailed account of the compound's synthesis and pharmacology in 1980 in the journal Communications in Psychopharmacology. Despite this publication, adrafinil remained an extremely obscure chemical for nearly two decades. The drug reached the French market in 1984 under the trade name Olmifon, with approval for narcolepsy treatment following in 1985.

    1994–2011

    While adrafinil was establishing its presence in European markets, its more potent metabolite modafinil continued through clinical development, receiving approval in France in 1994 and subsequently in the United States in 1998. Both compounds were marketed simultaneously, though modafinil gained significantly more international traction. In 2001, the American pharmaceutical company Cephalon acquired Laboratoires Lafon, gaining control of both adrafinil and modafinil products. A decade later, in September 2011, Cephalon voluntarily discontinued Olmifon following a reassessment by French regulatory authorities that determined the drug had an unfavorable risk-benefit ratio. While adrafinil was withdrawn from the legitimate pharmaceutical market, modafinil continued to be marketed globally. Following its pharmaceutical discontinuation, adrafinil gained renewed attention in the late 1990s and early 2000s as a commercially produced research chemical and purported nootropic supplement, particularly in markets where it remained unscheduled.

    Effect Profile

    Curated + 42 Reports
    Stimulant 7.0

    Strong stimulation, focus, and anxiety/jitters with low euphoria

    Stimulation / Energy×3
    109.9
    Euphoria / Mood Lift×2
    31.8
    Focus / Productivity×2
    108.1
    Anxiety / Jitters×1
    105.1
    Catalog Erowid

    Experience Report Analysis

    Erowid
    42 Reports
    2001–2020 Date Range
    17 With Age Data
    14 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 42 experience reports (42 Erowid)

    42 Reports
    14 Effects Detected
    7 Positive
    5 Adverse
    2 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 7

    Stimulation 59.5% 70%
    Focus Enhancement 40.5% 70%
    Euphoria 11.9% 70%
    Tactile Enhancement 11.9% 70%
    Empathy 9.5% 70%
    Music Enhancement 9.5% 70%
    Color Enhancement 7.1% 70%

    Adverse Effects 5

    Anxiety 23.8% 70%
    Headache 19.0% 70%
    Muscle Tension 11.9% 70%
    Nausea 7.1% 70%
    Increased Heart Rate 7.1% 70%

    Dose-Response Correlation

    How effect frequency changes across dose levels

    View data table
    Effect Common (n=11)
    Stimulation 81.8%
    Sedation 63.6%
    Anxiety 27.3%
    Increased Heart Rate 18.2%
    Psychosis 18.2%
    Focus Enhancement 18.2%
    Headache 18.2%
    Appetite Suppression 18.2%

    Dose–Effect Mapping

    Experience Reports

    How reported effects shift across dose tiers, based on 42 experience reports.

    Limited tier coverage — most reports fall within the Common range. Effects at other dose levels may not be represented.

    Oral dose range: 300.0–600.0 mg (median 300.0 mg)
    Effect Common (n=11)
    stimulation
    82%
    sedation
    64%
    anxiety
    27%
    increased heart rate
    18%
    psychosis
    18%
    focus enhancement
    18%
    headache
    18%
    appetite suppression
    18%

    Dosage Distribution

    Dose distribution from experience reports

    Median: 300.0 mg IQR: 300.0–600.0 mg n=21

    Real-World Dose Distribution

    62K Doses

    From 45 individual dose entries

    Oral (n=39)

    Median: 300.0mg 25th: 300.0mg 75th: 600.0mg 90th: 900.0mg
    mg/kg median: 4.628 mg/kg 75th: 7.544

    Form / Preparation

    Most common forms and preparations reported

    Body-Weight Dosing

    Dose relative to body weight from reports with weight data

    Median: 4.724 mg/kg IQR: 3.937–7.5 mg/kg n=20

    Redose Patterns

    Redosing behavior across 27 reports

    7.4% Redosed
    1.1 Avg Doses

    Legal Status

    World Anti-Doping Agency Prohibited List (2004)
    Country Status Notes
    France Withdrawn from market Originally approved for sale in 1981 and marketed under the trade name Olmifon as a prescription medication. In September 2011, the French regulatory authority (ANSM) reassessed the drug and withdrew marketing permission due to an unfavorable risk-benefit ratio.
    Laos Unregulated Reportedly available over-the-counter, though uncommon in practice.
    New Zealand Prescription only Classified as a prescription medicine following a 2005 recommendation by the Medical Classification Committee to MEDSAFE NZ, partly due to concerns about potential misuse as a party drug.
    South Africa Unregulated Reportedly available over-the-counter, though uncommon in practice.
    United States Unscheduled Not a controlled substance, meaning possession without a prescription or license is legal. However, the FDA considers adrafinil an unapproved drug and has taken multiple enforcement actions against companies selling it. In 2017, the FDA rejected a New Dietary Ingredient pre-market notification, stating it could not be concluded safe. Warning letters were issued in 2019, and criminal actions were undertaken in 2019 and 2022 against sellers. In 2023, an Arizona company was fined $2.4 million for introducing misbranded drugs including adrafinil into interstate commerce. Products containing adrafinil are subject to FDA import alerts, and the Department of Defense prohibits military service members from using adrafinil-containing products.
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