Adrafinil
Adrafinil is a eugeroic stimulant of the benzhydryl class that acts as a prodrug for modafinil.citation needed Discovered in 1974 by chemists at the French pharmaceutical company Laboratoires Lafon during screening for analgesic compounds, it was formerly marketed under the brand name Olmifon. It promotes wakefulness and alertness without amphetamine-like effects. Long-term use is not advised due to potential liver stress from elevated hepatic enzymes associated with its metabolism.
Dosage & Duration
Dosage
Doses are population estimates that vary widely between individuals.
Duration
Subjective Effects
Legacy content. A statistically backed ontology from Mindstate Design Labs is coming soon.
Effects vary widely by individual, dose, and context.
Physical
The physical effects of adrafinil can be broken down into several components.
Cognitive
The cognitive effects of adrafinil can be broken down into several components.
Pharmacology
Pharmacodynamics
Adrafinil is a prodrug that is primarily converted to modafinil in vivo, producing nearly identical pharmacological effects once the active metabolite has accumulated to sufficient concentrations.citation needed In animal studies, its locomotor-stimulating effects are blocked by α1-adrenergic and α2-adrenergic receptor antagonists, suggesting involvement of postsynaptic adrenergic signaling in its wakefulness-promoting activity. However, neither adrafinil nor modafinil has been found to bind the α1-adrenergic receptor directly, and the evidence for adrenergic agonism is considered weak. Modafinil has been identified as a weak, atypical inhibitor of the dopamine transporter, and this action may account for some or all of its pharmacological effects.
Pharmacokinetics
Adrafinil is metabolized hepatically and may follow one of two pathways: the primary route converts it to the active metabolite modafinil, while a secondary route produces inactive modafinilic acid directly without prior conversion to modafinil.citation needed This dual pathway may account for adrafinil's lower potency relative to modafinil. Modafinil is itself further metabolized to inactive modafinilic acid and modafinil sulfone. As a prodrug, adrafinil requires time for its active metabolite to accumulate to effective concentrations in the bloodstream.
Caution
Use cautionThese combinations are not usually physically harmful, but may produce undesirable effects, such as physical discomfort or overstimulation. Extreme use may cause physical health issues. Synergistic effects may be unpredictable. Care should be taken when choosing to use this combination.
Tolerance
Tolerance timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.
Benzhydryl eugeroics (modafinil, armodafinil)
Harm Potential
Addiction & Dependence
Psychological
LowAdrafinil is considered not addictive with a low potential for abuse. It does not appear to be capable of causing psychological dependence among most users.
Toxicity
Prolonged use may cause elevated liver enzymes and slight hepatotoxicity due to the requirement for hepatic metabolism to convert adrafinil to its active metabolite modafinil; occasional use at typical doses appears to carry minimal hepatic risk.
Psychosis Risk
Mania has been reported as a side effect, particularly in individuals with a predisposition to mood disorders such as bipolar disorder. Confusion, aggression, and overstimulation may also occur but are described as transitory effects that resolve upon discontinuation.citation needed
Seizure Risk
Adrafinil is contraindicated in individuals with epilepsy.citation needed
History & Culture
Discovery and Development
Adrafinil was discovered in 1974 by two chemists working at the French pharmaceutical company Laboratoires Lafon.citation needed The compound emerged unexpectedly during a screening program aimed at identifying novel analgesic agents. Rather than demonstrating pain-relieving…
Legality
International
World Anti-Doping Agency Prohibited List (2004)1
By Country
References
Source Pages
Citations
- Ameline A, Gheddar L, Raul JS, & Kintz P. (2020). Identification of adrafinil and its main metabolite modafinil in human hair. Self-administration study and interpretation of an authentic case. 5(4), 322-326. https://doi.org/10.1080/20961790.2019.17044821
- Poisons Standard. tga.gov.au (n.d.). https://www.tga.gov.au/resources/publication/publications/poisons-standard-february-20261
- Internationales Übereinkommen gegen Doping im Sport, Anlage I (Verbotsliste 2026; BGBl. III Nr. 219/2025). ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/Dokumente/BgblAuth/BGBLA_2025_III_219/BGBLA_2025_III_219.pdf1
- Internationales Übereinkommen gegen Doping im Sport, Anlage I (Verbotsliste 2026; BGBl. III Nr. 219/2025). ris.bka.gv.at (n.d.). https://ris.bka.gv.at/Dokumente/Bundesnormen/NOR40275236/NOR40275236.html1
- Internationales Übereinkommen gegen Doping im Sport, Anlage I (Verbotsliste 2026; BGBl. III Nr. 219/2025). ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/NormDokument.wxe?Abfrage=Bundesnormen&Gesetzesnummer=20011421&Paragraf=1&Uebergangsrecht=1
- Lei nº 14.597/2023, art. 175, VIII; Lista Proibida 2026 do Código Mundial Antidopagem. planalto.gov.br (n.d.). https://www.planalto.gov.br/ccivil_03/_ato2023-2026/2023/lei/l14597.htm1
- Lei nº 14.597/2023, art. 175, VIII; Lista Proibida 2026 do Código Mundial Antidopagem. gov.br (n.d.). https://www.gov.br/abcd/pt-br/composicao/atletas/substancias-e-metodos-proibidos/arquivos-lista-de-substancias-proibidas/lista_proibida_2026_pt-br_v-3semlogo.pdf/%40%40download/file1
- Lei nº 14.597/2023, art. 175, VIII; Lista Proibida 2026 do Código Mundial Antidopagem. gov.br (n.d.). https://www.gov.br/esporte/pt-br/noticias-e-conteudos/esporte/abcd-divulga-lista-de-substancias-e-metodos-proibidos-20261
- 2026年兴奋剂目录公告;《反兴奋剂条例》. sport.gov.cn (n.d.). https://www.sport.gov.cn/kjs/n5084/c29328536/part/29328879.pdf1
- 2026年兴奋剂目录公告;《反兴奋剂条例》. samr.gov.cn (n.d.). https://www.samr.gov.cn/zw/zfxxgk/fdzdgknr/bgt/art/2023/art_ab59ecfc91ce456399fcf3357ea54622.html1
Further Reading
Article Status
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Recent changes8 human edits · latest
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13 August 2026
Lyrea · Updated the article
24 January 2026
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
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