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AB-FUBINACA

AB-FUBINACA molecule structureAB-FUBINACA molecule structure
Ab-fubi
Psychoactive Class

AB-FUBINACA is a synthetic cannabinoid of the indazolecarboxamide class.1 Originally developed by Pfizer in 2009citation needed as an analgesic, it was never pursued for human use and first surfaced in synthetic cannabinoid blends in Japan in 2012. It is a highly potent cannabinoid receptor agonist,2 and its extreme potencycitation needed—combined with its widespread inclusion in unregulated herbal blends—poses significant overdose risk, with fatalities reported.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~0.25 mg
Light0.25-0.5 mg
Moderate0.5-1.5 mg
Strong1.5-3 mg
Heavy3+ mg

Subjective Effects

Legacy content. A statistically backed ontology from Mindstate Design Labs is coming soon.

Effects vary widely by individual, dose, and context.

Physical

Perception of increased weightPerception of decreased weight

Cognitive

Auditory

Forked from Subjective Effect Documentation work byJosie Kins September 2015.

Reagent Testing

Expected colorimetric results for common reagent tests. Colors show reaction change over 1–2 minutes.

Mecke(ME)
white → black2
Marquis(MQ)
No reaction
No reaction
Mandelin(MD)
No reaction
No reaction
Liebermann(LB)
No reaction
No reaction
Powered by PROtestkit.eu

Pharmacology

Pharmacodynamics

AB-FUBINACA acts as a potent agonist at both major cannabinoid receptors, with notably high affinity and potency at CB1 (Ki of 0.9 nMcitation needed, EC50 of 1.8 nM3). It also binds CB2, though with lower affinity (Ki of 23.2 nM). Its pronounced CB1 activity at sub-nanomolar concentrations underlies its extremely high potency relative to many other cannabinoid receptor ligands.

Pharmacokinetics

Absorption & half-lifenot documented yetMetabolitesnone documented yet

Interactions

Interactions not written up yet

An unlisted combination is an unknown one, not a safe one. Check a dedicated combination chart before mixing.

Check TripSit

Tolerance

Tolerance timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.

Cross Tolerance

Cannabinoids (both synthetic and plant-derived)

Harm Potential

Addiction & Dependence

Psychological

Low

Classified as habit-forming. Psychological dependence may develop with regular use, similar to other synthetic cannabinoids.citation needed

Toxicity

Lethal Dosage

Its extremely high potency and inclusion in synthetic cannabinoid blends make it dangerous, and it has caused death in overdose, with use linked to hospitalizations and fatalities. In an August 2018 event in New Haven, Connecticut, over 100 people required emergency transport after using synthetic cannabis containing AB-FUBINACA, with several in critical or life-threatening condition; no deaths resulted from that incident, and first responders attributed those overdoses to opiate adulterants.

History & Culture

AB-FUBINACA was initially synthesized by Pfizer in 2009 during research into novel analgesic compounds.citation needed The pharmaceutical company never advanced the substance to human clinical trials, and it was subsequently abandoned as a potential medication.

Legality

International

AB-FUBINACA is included in Schedule II of the 1971 Convention on Psychotropic Substances. It was placed under international control in 2020.

By Country

Illegal14
United States flagUnited StatesIllegal
Austria flagAustriaIllegal
Brazil flagBrazilIllegal
Canada flagCanadaIllegal
China flagChinaIllegal
Denmark flagDenmarkIllegal
Finland flagFinlandBanned
Ireland flagIrelandIllegal
Japan flagJapanIllegal
Netherlands flagNetherlandsIllegal
Norway flagNorwayIllegal
Philippines flagPhilippinesIllegal
Singapore flagSingaporeIllegal
Thailand flagThailandIllegal
Controlled / restricted3
Australia flagAustraliaRestricted
Germany flagGermanyRestricted
Spain flagSpainRestricted

References

Source Pages

  1. Erowid Experience Vaults: AB-FUBINACA
  2. PsychonautWiki: AB-FUBINACA
  3. Wikipedia

Citations

  1. Michael Hsin-Hung Chen, Aybike Dip, Mostafa Ahmed, Michael L. Tan, Jeffrey P. Walterscheid, Hua Sun, Ba-Bie Teng, & Ashraf Mozayani. (2016). Detection and Characterization of the Effect of AB-FUBINACA and Its Metabolites in a Rat Model. Journal of Cellular Biochemistry, 117(4), 1033–1043. https://doi.org/10.1002/jcb.254211
  2. Samuel D. Banister, Michael Moir, Jordyn Stuart, Richard C. Kevin, Katie E. Wood, Mitchell Longworth, Shane M. Wilkinson, Corinne Beinat, Alexandra S. Buchanan, Michelle Glass, Mark Connor, Iain S. McGregor, & Michael Kassiou. (2015). Pharmacology of Indole and Indazole Synthetic Cannabinoid Designer Drugs AB-FUBINACA, ADB-FUBINACA, AB-PINACA, ADB-PINACA, 5F-AB-PINACA, 5F-ADB-PINACA, ADBICA, and 5F-ADBICA. ACS Chemical Neuroscience, 6(9), 1546–1559. https://doi.org/10.1021/acschemneuro.5b001121
  3. Sunjoo Kim, Dong Kyun Kim, Yongho Shin, Ji-Hyeon Jeon, Im-Sook Song, & Hye Suk Lee. (2020-10-08). In Vitro Interaction of AB-FUBINACA with Human Cytochrome P450, UDP-Glucuronosyltransferase Enzymes and Drug Transporters. Molecules, 25(19), Article 4589. https://doi.org/10.3390/molecules251945891234
  4. World Health Organization. (2019). AB-FUBINACA: Critical Review Report. https://ecddrepository.org/sites/default/files/2023-04/final_ab-fubinaca.pdf1
  5. Dan Vergano. (2018). Experts Are Worried About A New Wave Of Dangerous Synthetic Cannabis. BuzzFeed News. https://www.buzzfeednews.com/article/danvergano/synthetic-marijuana-spice-ab-fubinaca-overdoses1
  6. Customs (Prohibited Imports) Regulations 1956. legislation.gov.au (n.d.). https://www.legislation.gov.au/F1996B03651/2026-03-26/2026-03-26/text/original/epub/OEBPS/document_1/document_1.html1
  7. Suchtgiftverordnung, Anhang IV. ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/eli/bgbl/ii/1997/374/ANL4/NOR402674551
  8. RDC ANVISA nº 999, de 24 de novembro de 2025. gov.br (n.d.). https://www.gov.br/anvisa/pt-br/assuntos/medicamentos/controlados/RDC9992025.pdf/@@display-file/file1
  9. Schedule II, Controlled Drugs and Substances Act. laws-lois.justice.gc.ca (n.d.). https://laws-lois.justice.gc.ca/eng/acts/C-38.8/section-sched95540.html?wbdisable=true1
  10. 我国管制毒品目录(2026年7月更新,540种+三大类), Shenzhen Public Security Bureau, published 17 July 2026. ga.sz.gov.cn (n.d.). https://ga.sz.gov.cn/SZJDZX/SZBMFW/content/post_12898420.html1

Further Reading

  1. NCBI: Overview of Synthetic Cannabinoids ADB-FUBINACA and AMB-FUBINACA
  2. NCBI: The short-acting synthetic cannabinoid AB-FUBINACA induces physical dependence in mice
  3. Trecki et al. 2015: Synthetic Cannabinoid-Related Illnesses and Deaths
  4. WHO Expert Committee on Drug Dependence: AB-FUBINACA Critical Review

Article Status

  • Josie Kins avatar
    Step 1 · Automated synthesis

    An autonomous workflow built by Josie Kins compiled this article's foundation from information published across the web.

  • Step 2 · First-pass reviewPending

    Not yet reviewed — this article is pending editorial review by Lyrea.

  • Step 3 · Citation reviewPending

    No one has reviewed this article's citations yet. That second pass checks each claim against the source it cites.

Recent changes7 human edits · latest

Times are UTCNewest first

24 January 2026

  1. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  2. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  3. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  4. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  5. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  6. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  7. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

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