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Pharmakon Plants Tabernanthe iboga
Apocynaceae · Gentianales · Angiosperms

Tabernanthe iboga

Iboga · eboka · éboga · bois sacré · sacred wood
Human history nineteenth-century documentation · older transmission histories · IUCN Least Concern · 2019 assessment

Botany

Accepted nameTabernanthe iboga Baill. Kew accepts the species; Henri Baillon published the name in Bulletin Mensuel de la Société Linnéenne de Paris 1:783 in 1888 (Baillon, 1888; POWO, 2026).
FamilyApocynaceae · subfamily Rauvolfioideae · tribe Tabernaemontaneae in current classifications.
OrderGentianales.
Native rangeWest-central tropical Africa south to Angola. Kew’s broad range includes the Congo Basin and Atlantic equatorial forest; floristic and ethnobotanical records centre especially on Gabon, Cameroon, Equatorial Guinea, Republic of the Congo, Democratic Republic of the Congo and Cabinda/Angola (POWO, 2026; Pope, 1969).
HabitatsMoist lowland evergreen forest and secondary forest, commonly in shaded understory and forest margins. Long cultivation beside houses, villages and ritual sites complicates a strict wild/cultivated distinction.
Local namesIboga, eboka/éboga and related forms occur across several regional languages; French-language sources commonly use bois sacré. Vernacular vocabularies can distinguish cultivated forms by fruit shape, potency, provenance or ritual valuation; names should not be assumed to map one-to-one onto botanical taxa (Pope, 1969; Fernandez, 1982; Samorini, 2025a).
SynonymyHistorical names placed in synonymy include Iboga vateriana, Tabernanthe albiflora, T. bocca, T. mannii, T. pubescens, T. subsessilis and T. tenuiflora. Vonk’s revision retained T. iboga and T. elliptica as the genus’s two species (Vonk, 1989; POWO, 2026).

Morphology and life history

An evergreen, much-branched shrub commonly about 1–3 m tall, occasionally developing into a small tree approaching 10 m. Opposite leaves are simple, narrow-elliptic to lanceolate, glossy dark green above and paler beneath. Like many Apocynaceae it exudes milky latex when injured. Small, fragrant, tubular flowers are white to yellowish or pink-tinged and borne in compact axillary clusters. The paired fruits mature yellow to orange and range from subglobose to elongate or fusiform; their fleshy pulp encloses numerous seeds. A thick yellowish root system supports the plant, while the outer root tissues are the principal harvested alkaloid source (Schultes and Hofmann, 1980; Pope, 1969).

The concentration of valued alkaloids in root cortex creates a conservation problem unlike leaf harvest: stripping or uprooting may debilitate or kill a slow-establishing shrub. Cultivated plants can be raised from seed and propagated vegetatively, but seed viability, provenance and years to substantial root formation affect restoration and supply. Cultivation is therefore both biological management and a social question about who controls land, germplasm, labour and ceremonial access (Ermakova et al., 2025; ICEERS, 2026).

Identification and taxonomic limits

Field useful

Opposite glossy leaves, milky latex, small salverform flowers and paired orange-yellow fruits support identification when reproductive material is available.

Dried trade

Powdered or chipped “iboga” root cannot be authenticated reliably by appearance. Commercial surveys have found wide alkaloid variation and substitution risks; voucher specimens and validated chemical methods are necessary (Bouso et al., 2020).

Vernacular forms

Descriptions of “male” and “female,” round- and long-fruited, or strong and weak iboga are important ethnobotanical classifications. They are not automatically equivalent to botanical sex, separate species or reproducible chemotypes.

Chemistry

Iboga contains a structurally elaborate ensemble of monoterpene indole alkaloids. Ibogaine is usually the most discussed constituent of root bark, but whole-root preparations also contain ibogamine, tabernanthine, ibogaline, iboxygaine, voacangine, coronaridine and further minor alkaloids. Abundance depends on tissue, plant, provenance, storage and method. Noribogaine is most important pharmacologically as the active human metabolite formed largely through CYP2D6, not as a synonym for the plant’s native alkaloid profile (Bading-Taika et al., 2018; Iyer et al., 2021).

Ibogaine

C₂₀H₂₆N₂O
12-methoxyibogamine
Principal studied iboga alkaloid · long-acting polypharmacology

Ibogamine

C₁₉H₂₄N₂
Parent iboga alkaloid scaffold
Root-bark constituent · biological contribution incompletely resolved

Tabernanthine

C₂₀H₂₆N₂O
Methoxyibogamine positional isomer
Named from Tabernanthe · one component of whole-root chemistry

Voacangine

C₂₂H₂₈N₂O₃
Carbomethoxy-methoxy iboga alkaloid
Biosynthetic relative and semisynthetic ibogaine precursor

Distribution, biosynthesis and metabolism

One characterised powder contained 1.93% ibogaine by dry weight, with ibogaine contributing about one quarter of detected chromatographic alkaloid signal; that figure is a specimen result, not a species constant (Bading-Taika et al., 2018). Analysis of retail materials reported root-bark products ranging roughly 0.6–11.2% ibogaine, demonstrating why labels, colour and declared mass cannot establish composition (Bouso et al., 2020). Enzymatic studies identified coronaridine hydroxylation and methylation steps in the plant’s route to ibogaine and later reconstructed the pathway to voacangine, opening non-extractive routes to related alkaloids (Farrow et al., 2018; 2019).

In humans, ibogaine is lipophilic and is O-demethylated principally by CYP2D6 to noribogaine. Genetic metaboliser status, liver function and interacting medicines can change exposure. Ibogaine and noribogaine have different time courses and target profiles; noribogaine persists longer and has prominent serotonin-transporter and opioid-receptor activity. Neither compound is well represented by the shorthand “a 5-HT₂A psychedelic” (Glue et al., 2016; Knuijver et al., 2024).

Neuropharmacology and toxicology

Polypharmacology

Ibogaine interacts with NMDA, nicotinic acetylcholine, opioid and sigma receptors and with monoamine transporters, with affinities and functional effects varying by assay and concentration. No single target adequately explains the acute state or reported anti-addictive effects (Wasko, Witt-Enderby and Surratt, 2018; Iyer et al., 2021).

Cardiac hazard

Ibogaine and noribogaine inhibit hERG potassium channels and can prolong ventricular repolarisation. Bradycardia, QT/QTc prolongation, ventricular arrhythmia, torsades de pointes and sudden death are documented (Koenig and Hilber, 2015; Alper, Stajić and Gill, 2012).

Plasticity research

Animal and cell studies report neurotrophic or psychoplastogenic effects and reduced drug-seeking for some analogues. Translation to durable human benefit remains unproved, and non-hallucinogenic congeners are pharmacologically new drugs rather than safer iboga by definition (Cameron et al., 2021; Havel et al., 2024).

Whole plant

No controlled trial establishes equivalence among root bark, total-alkaloid extracts, purified ibogaine hydrochloride, noribogaine or synthetic analogues. Findings from one cannot be transferred automatically to another.

Tradition, ritual & cultural use

Oldest evidenced or proposed human use

Before writingOral histories Regional accounts frequently credit forest-dwelling Babongo and related communities with discovering iboga and transmitting it to neighbouring peoples. These narratives record relations among forest specialists, migrants and ritual institutions; they do not presently yield a datable single origin event (Fernandez, 1982; Samorini, 2025b).
1819 “eroga”Uncertain Thomas Bowdich described a violent medicine called “eroga” as a fungus growing on a decaying tree. The similar name makes this a possible distorted notice of iboga, but the organism and preparation do not securely identify T. iboga (Bowdich, 1819; Samorini, 2024a).
1864 reportBotanical / colonial Aubry-Lecomte, drawing on Griffon du Bellay’s Gabon collections, described iboga root chewed in small quantities by hunters and warriors to remain awake and identified it as an apocynaceous plant. This is the earliest clear printed notice (Aubry-Lecomte, 1864).
1888 descriptionTaxonomy Baillon formally named Tabernanthe iboga. Botanical description made the plant legible to colonial science but did not begin its local history (Baillon, 1888).
Late 19th–20th c.Institutional change Bweté/Bwiti forms moved among southern Gabonese peoples and into Fang-speaking regions, where ancestor institutions, colonial disruption and Christian imagery generated new branches. Dating differs by locality; “Bwiti” never designated a single unchanging church (Fernandez, 1982; Mary, 1983; Bonhomme, 2023).

Peoples, territories and traditions

Ritual practice, shamanism and healing

The relevant specialists are variously nganga, lineage elders, harpists, singers, dancers, attendants and office-holders; translating every role as “shaman” erases this division of ritual labour. Initiation makes a banzi/banzie through collective supervision rather than private intoxication. Preparation can include seclusion, fasting, bathing, confession, bodily marking and instruction. During the central night or sequence of nights, the initiate commonly reclines near the ceremonial action while attendants monitor bodily condition, sustain music and ask what is being seen. The event culminates in public recognition, teaching and return to ordinary social relations (Fernandez, 1972; 1982).

InitiationA large, ritually judged ingestion of root material may be distributed through the night. The initiate’s passage is narrated as death, encounter and rebirth. This entry omits quantities: ethnographic authority is not a reproducible toxicological protocol.
Nocturnal worshipSmaller amounts can sustain wakefulness during recurring ngoze services of song, dance, teaching and collective remembrance. Stimulant and visionary uses exist on a continuum but have different ritual purposes (Fernandez and Fernandez, 2001).
Diagnosis and healingIn healing cults, illness may involve spirits, ancestors, broken relations, envy, place or bodily disorder. Vision is tested through questions, divination and later consequences; seeing an image is not yet a diagnosis (Bonhomme, 2005).
Forest and medicineIboga may accompany other plant medicines, baths and protective preparations. The species is a privileged sacrament but not the total pharmacopeia of any documented community.

Fernandez described the ritual aim as a return to “the path of life and death” and “the work of the ancestors” (Fernandez and Fernandez, 2001, pp. 235–269). These compact phrases locate healing in genealogy and obligation: the initiate does not simply acquire an extraordinary private state but is re-situated between the dead and unborn, village and forest, personal biography and collective history.

Cosmology & key terms

Plural origin narratives

There is no single canonical iboga myth. In a widely reported Mitsogo narrative cycle, a woman—named or associated with Disumba in some tellings—first consumes iboga, crosses into the world of the dead and is subsequently killed or sacrificed. Her remains become ritual instruments or founding substances; her voice becomes the ngombi harp. A male culture hero returns with knowledge, relics or the means to build the first temple. Versions redistribute agency, gender and guilt, and later Fang tellings may identify figures through Christian names or biblical history (Fernandez, 1982; Samorini, 2024b).

The plant’s downward-growing root readily participates in a vertical cosmology of earth and ancestors, while the all-night ceremony moves through darkness toward dawn. Yet “underworld,” “death” and “rebirth” are analytical translations of locally elaborated places, persons and routes. Bweté cosmology is also historical: ancestors legitimise fertility and descent, Christian symbols can articulate colonial encounter, and national or urban predicaments enter sermon, song and vision (Fernandez, 1982; Mary, 1983).

Art, sound and ceremonial space

Music as visionary technique

Music supplies pulse, direction, memory and interpersonal control across a state that can last far longer than the most image-rich phase. Repeated ostinati, accelerating dance, antiphonal singing and instrumental timbres can be heard as voices, vehicles or presences. The ensemble also keeps the surrounding community awake and able to witness the initiate. Phenomenology is therefore jointly produced by alkaloids, darkness, fatigue, sound, expectation, bodily position and questioning; the chemistry is necessary to describe the drug state but insufficient to describe the ritual world (Fernandez, 1972; Maas and Strubelt, 2003).

Visionary phenomenology

Onsetoften 1–3 h · variable plant material and context
Visionary phasecommonly several hours · eyes-closed, narrative imagery
Evaluative phaseroughly 8–20 h · wakeful autobiographical review
Residual coursefatigue, stimulation or disequilibrium may persist 24–72 h

Durations are approximate syntheses from ibogaine studies and ethnographic descriptions, not a timetable for root bark. Plant composition, metabolism, co-administered substances, fasting and ceremonial pacing all alter the course. Traditional initiations may surround the acute pharmacology with two or more days of preparation, night work and recovery (Fernandez, 1982; Kohek et al., 2020).

Recurrent experiential sequence

Somatic thresholdIntense bitterness and oral numbness may be followed by nausea, vomiting, tremor, oscillating heat and cold, buzzing or roaring, heaviness and severe ataxia. Lying still with eyes closed often becomes necessary. Somatic distress is prominent rather than incidental.
Oneiric displayRapid, film-like sequences; faces, animals, ancestors and deceased relatives; distant landscapes, processions, luminous beings and frightening scenes. Imagery is often described as representational and narrative rather than the continuously geometric field typical of some serotonergic psychedelics (Kohek et al., 2020).
Autobiographical replayChildhood episodes, trauma, relationships and morally charged decisions may be reviewed from a detached “observer” position. Scenes can feel shown by an intelligent interlocutor, ancestor or the plant, and may answer questions posed by attendants.
EvaluationAs images recede, prolonged wakefulness supports analytic review, remorse, forgiveness, purpose or plans for change. Contemporary treatment narratives often identify this evaluative phase as central to perceived benefit (Rodríguez-Cano et al., 2023).
ReturnEmotional openness and cognitive clarity may coexist with exhaustion, insomnia and bodily instability. Ritual return is socially marked; clinical “integration” is a later institution with different concepts and authorities.

Accounts and interpretation

Kohek and colleagues’ interviews with twenty ibogaine users identified physical, sensory, visual, auditory, cognitive, adverse and after-effect domains, including ancestors and entities, landscapes, horrific scenes, self-analysis, empathy, catharsis, ego dissolution and spiritual states (Kohek et al., 2020). A separate qualitative study of underground treatment emphasised autobiographical memory, interpersonal and transpersonal experience, preparation, integration and motivation for lifestyle change (Rodríguez-Cano et al., 2023). These samples are self-selected and do not establish frequency in all users.

> It was like watching my life as a film, but I could stop and speak to the people in it. — — paraphrased composite of recurrent interview descriptions; Kohek et al. (2020), not a verbatim single-participant quotation

The composite is labelled because striking internet quotations often lose provenance. Ethnographically, an image of a dead relative may be recognised as ancestral communication; psychologically, it may be coded as autobiographical memory or grief processing; neurologically, it remains a subjective report correlated with a drug state. The descriptions can coexist as different explanatory registers without being collapsed into one another.

In 2026, analysis of post-session narratives from thirty male Special Operations veterans reported four recurring domains: dialogic trauma reappraisal and guided replay; altered self and mystical connectedness; emotional resolution through forgiveness, love and purpose; and embodied healing or clarity (Olash et al., 2026). The cohort had received magnesium–ibogaine with complementary care in Mexico. Its language cannot be treated as Bwiti phenomenology or as controlled evidence that a particular vision caused clinical change.

Contemporary status

Conservation, harvest and economies

T. iboga is globally assessed as Least Concern, reflecting its broad range rather than abundance at every harvest site (BGCI and IUCN SSC Global Tree Specialist Group, 2019). Forest loss, destructive root harvest and international demand can nevertheless produce local scarcity. Gabonese ceremonial markets, village cultivation, cross-border wild harvest, internet retail, retreat tourism and pharmaceutical research form overlapping economies with very unequal prices and authority (Ermakova et al., 2025; INTERPOL, 2023).

Global assessment

Least Concern is not a certificate of sustainable trade. Population trend, harvest mortality, provenance and replacement rates remain poorly quantified.

Trafficking

INTERPOL documented illicit extraction and transnational trafficking of iboga among natural psychotropics. A 2026 participatory report states that officially legal export from Gabon was again prohibited while illicit networks continued (INTERPOL, 2023; ICEERS, 2026).

Cultivation

Community nurseries, non-destructive root management, seed provenance and benefit-sharing can reduce pressure, but sustainability claims require traceable land and harvest data.

Alternative supply

Semisynthesis from Voacanga africana, biosynthesis and efficient total synthesis may reduce pharmaceutical demand for iboga root. They do not by themselves support Gabonese cultivators or maintain ritual access (Farrow et al., 2019; Iyer et al., 2025).

Law, access and benefit-sharing

InternationalIbogaine is not scheduled by the 1961 or 1971 UN drug conventions. National law therefore varies. T. iboga is not listed in the CITES Appendices as of August 2026 (INCB, 2026; CITES, 2026).
GabonRitual use remains culturally recognised, while access to wild populations and export are regulated. Gabon’s Nagoya Protocol framework makes prior informed consent, authorised access and benefit-sharing central to legal genetic-resource trade. Pilot Nagoya-compliant exports occurred in 2023–24; the 2026 policy report records a subsequent official export prohibition pending legal development (CBD, 2026; ICEERS, 2026).
United StatesIbogaine remains a federal Schedule I substance and no ibogaine medicine is FDA-approved. An executive order of 18 April 2026 directs agencies to facilitate research and a Right-to-Try pathway for eligible patients, including necessary Schedule I permissions; it does not itself deschedule ibogaine or establish efficacy (DEA, 2025; The White House, 2026).
France / UKFrance controls iboga and ibogaine as narcotics. In the United Kingdom ibogaine is not named in the standard controlled-drugs list, but production, supply, import or export for psychoactive use may fall under the Psychoactive Substances Act 2016. Legal status depends on jurisdiction and conduct; this is not legal advice.
Treatment travelClinics and retreats operate in Mexico, Costa Rica, Brazil, South Africa, New Zealand and elsewhere under differing medical, pharmaceutical and consumer-protection rules. “Not scheduled” is not equivalent to licensed therapy.

Patents and translation

Howard Lotsof’s 1985 US patent 4,499,096 claimed a method of interrupting narcotic addiction with ibogaine; later patents extended claims across cocaine, alcohol, nicotine and polysubstance dependence (Lotsof, 1985). Contemporary portfolios concern noribogaine, purified formulations, salts, analogues, methods of treatment and potentially less cardiotoxic congeners. A patent grants limited claims in a jurisdiction; it does not establish safety, approval, ownership of T. iboga as a species or ownership of Bwiti knowledge. The policy issue is how invention, prior art, genetic-resource access and benefits to source communities are documented (Bonhomme, 2023).

Clinical and neuroscience research

Open-label and observational studies in opioid-dependent participants report rapid reduction of withdrawal and craving and, in some cohorts, reduced subsequent use. They also contain selection bias, variable psychosocial care and limited controls; one New Zealand cohort included a death during treatment (Brown and Alper, 2018; Noller, Frampton and Yazar-Klosinski, 2018; Mash et al., 2018). A monitored open-label safety study documented frequent QTc prolongation and clinically important bradycardia, reinforcing rather than resolving cardiac risk (Knuijver et al., 2022). The registered Phase I/IIa opioid-withdrawal study NCT05029401 has not had its status verified within two years and is treated by ClinicalTrials.gov as unknown/closed (ClinicalTrials.gov, 2026).

The research frontier is active but asymmetrical: sophisticated chemistry and human neuroimaging now coexist with sparse population ecology, limited pharmacognosy of ceremonial material and relatively little funded scholarship led by Gabonese practitioners and scientists. A species monograph must keep these evidentiary scales visible.

Bibliography

Harvard style (Cite Them Right) · DOI and stable-record links · 54 sources

Archaeology & history

01 · 6 sources
Aubry-Lecomte, C.E. (1864) ‘Note sur quelques poisons de la côte occidentale d’Afrique’, Revue Maritime et Coloniale, 12, pp. 464–468.
colonial botanical record
Bonhomme, J. (2023) ‘From Bwiti to ibogaine and back: a transnational history of Tabernanthe iboga’, in Langlitz, N. et al. (eds.) Expanding Mindscapes. Cambridge, MA: MIT Press, pp. 189–214. Available at: https://doi.org/10.7551/mitpress/14417.003.0014.
DOI checked
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Bowdich, T.E. (1819) Mission from Cape Coast Castle to Ashantee. London: John Murray, p. 422.
ambiguous early record
Pope, H.G. (1969) ‘Tabernanthe iboga: an African narcotic plant of social importance’, Economic Botany, 23, pp. 174–184. Available at: https://doi.org/10.1007/BF02860623.
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Samorini, G. (2024a) ‘Studies on the iboga cults. I. The ancient documents’, Antrocom Online Journal of Anthropology, 20(1), pp. 93–114. Available at: samorini.it.
open article
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Samorini, G. (2025b) ‘Studies on the iboga cults V: historical aspects’, Antrocom Online Journal of Anthropology, 21(1).
specialist synthesis

Botany & taxonomy

02 · 4 sources
Baillon, H.E. (1888) ‘Tabernanthe iboga’, Bulletin Mensuel de la Société Linnéenne de Paris, 1, p. 783.
protologue
BGCI and IUCN SSC Global Tree Specialist Group (2019) ‘Tabernanthe iboga’, The IUCN Red List of Threatened Species, e.T120678584A143718006. Available at: iucnredlist.org.
global assessment
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Plants of the World Online (POWO) (2026) ‘Tabernanthe iboga Baill.’ Royal Botanic Gardens, Kew. Available at: powo.science.kew.org (Accessed: 7 August 2026).
accepted taxonomy
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Vonk, G.J.A. (1989) ‘Revision of the genus Tabernanthe (Apocynaceae)’, Mededelingen Landbouwhogeschool Wageningen, 89(4), pp. 1–18.
taxonomic revision

Chemistry & pharmacology

03 · 11 sources
Alper, K.R., Stajić, M. and Gill, J.R. (2012) ‘Fatalities temporally associated with the ingestion of ibogaine’, Journal of Forensic Sciences, 57(2), pp. 398–412. Available at: https://doi.org/10.1111/j.1556-4029.2011.02008.x.
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Bading-Taika, B. et al. (2018) ‘Phytochemical characterization of Tabernanthe iboga root bark and its effects on dysfunctional metabolism and cognitive performance in high-fat-fed C57BL/6J mice’, Journal of Food Bioactives, 3, pp. 111–123. Available at: https://doi.org/10.31665/JFB.2018.3154.
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Bartlett, M.F., Dickel, D.F. and Taylor, W.I. (1958) ‘The alkaloids of Tabernanthe iboga. Part IV: the structures of ibogamine, ibogaine, tabernanthine and voacangine’, Journal of the American Chemical Society, 80(1), pp. 126–136. Available at: https://doi.org/10.1021/ja01534a036.
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Bouso, J.C. et al. (2020) ‘An analytical study of iboga alkaloids contained in Tabernanthe iboga-derived products offered by ibogaine treatment providers’, Revista de Psiquiatria Clínica, 47(2), pp. 45–51. Available at: https://doi.org/10.1590/0101-60830000000231.
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Farrow, S.C. et al. (2018) ‘Cytochrome P450 and O-methyltransferase catalyze the final steps in the biosynthesis of the anti-addictive alkaloid ibogaine from Tabernanthe iboga’, Journal of Biological Chemistry, 293(36), pp. 13821–13833. Available at: https://doi.org/10.1074/jbc.RA118.004060.
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Farrow, S.C. et al. (2019) ‘Biosynthesis of an anti-addiction agent from the iboga plant’, Journal of the American Chemical Society, 141(33), pp. 12979–12983. Available at: https://doi.org/10.1021/jacs.9b05999.
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Havel, V., Kruegel, A.C., Bechand, B. et al. (2024) ‘Oxa-iboga alkaloids lack cardiac risk and disrupt opioid use in animal models’, Nature Communications, 15, 8118. Available at: https://doi.org/10.1038/s41467-024-51856-y.
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Iyer, R.N., Favela, D., Zhang, G. and Olson, D.E. (2021) ‘The iboga enigma: the chemistry and neuropharmacology of iboga alkaloids and related analogs’, Natural Product Reports, 38(2), pp. 307–329. Available at: https://doi.org/10.1039/D0NP00033G.
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Iyer, R.N., Zhou, X., Akins, N.S. et al. (2025) ‘Efficient and modular synthesis of ibogaine and related alkaloids’, Nature Chemistry, 17, pp. 412–420. Available at: https://doi.org/10.1038/s41557-024-01714-7.
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Koenig, X. and Hilber, K. (2015) ‘The anti-addiction drug ibogaine and the heart: a delicate relation’, Molecules, 20(2), pp. 2208–2228. Available at: https://doi.org/10.3390/molecules20022208.
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Wasko, M.J., Witt-Enderby, P.A. and Surratt, C.K. (2018) ‘DARK classics in chemical neuroscience: ibogaine’, ACS Chemical Neuroscience, 9(10), pp. 2475–2483. Available at: https://doi.org/10.1021/acschemneuro.8b00294.
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Clinical research & neuroscience

04 · 11 sources
Brown, T.K. and Alper, K. (2018) ‘Treatment of opioid use disorder with ibogaine: detoxification and drug use outcomes’, The American Journal of Drug and Alcohol Abuse, 44(1), pp. 24–36. Available at: https://doi.org/10.1080/00952990.2017.1320802.
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Cherian, K.N., Kulas, J.A., Evans, L.K. et al. (2024) ‘Magnesium–ibogaine therapy in veterans with traumatic brain injuries’, Nature Medicine, 30, pp. 373–381. Available at: https://doi.org/10.1038/s41591-023-02705-w.
DOI checked
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ClinicalTrials.gov (2026) ‘A study of oral ibogaine in opioid withdrawal’, NCT05029401. Available at: clinicaltrials.gov (Accessed: 7 August 2026).
status unknown
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Esperança, M.P., Ataíde, A., Vieira-Coelho, M.A. and Borges, J.P. (2026) ‘Ibogaine: therapeutic potential, cardiac safety, and clinical considerations in substance use disorder treatment’, Molecules, 31(3), 545. Available at: https://doi.org/10.3390/molecules31030545.
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Glue, P. et al. (2016) ‘Ascending single-dose, double-blind, placebo-controlled safety study of noribogaine in opioid-dependent patients’, Clinical Pharmacology in Drug Development, 5(6), pp. 460–468. Available at: https://doi.org/10.1002/cpdd.254.
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Knuijver, T. et al. (2024) ‘The pharmacokinetics and pharmacodynamics of ibogaine in opioid use disorder patients’, Journal of Psychopharmacology, 38(5), pp. 481–488. Available at: https://doi.org/10.1177/02698811241237873.
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Knuijver, T., Schellekens, A.F.A., Belgers, M. et al. (2022) ‘Safety of ibogaine administration in detoxification of opioid-dependent individuals: a descriptive open-label observational study’, Addiction, 117(1), pp. 118–128. Available at: https://doi.org/10.1111/add.15448.
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Lissemore, J.I., Cao, S., Kulas, J.A. et al. (2025) ‘Magnesium–ibogaine therapy effects on cortical oscillations and neural complexity in veterans with traumatic brain injury’, Nature Mental Health, 3, pp. 918–931. Available at: https://doi.org/10.1038/s44220-025-00463-x.
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Mash, D.C., Duque, L., Page, B. and Allen-Ferdinand, K. (2018) ‘Ibogaine detoxification transitions opioid and cocaine abusers between dependence and abstinence: clinical observations and treatment outcomes’, Frontiers in Pharmacology, 9, 529. Available at: https://doi.org/10.3389/fphar.2018.00529.
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Noller, G.E., Frampton, C.M. and Yazar-Klosinski, B. (2018) ‘Ibogaine treatment outcomes for opioid dependence from a twelve-month follow-up observational study’, The American Journal of Drug and Alcohol Abuse, 44(1), pp. 37–46. Available at: https://doi.org/10.1080/00952990.2017.1310218.
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Sridhar, M. et al. (2026) ‘Neural correlates of ibogaine: evidence from functional neuroimaging of military veterans’, Biological Psychiatry: Cognitive Neuroscience and Neuroimaging, 11(6), pp. 624–633. Available at: https://doi.org/10.1016/j.bpsc.2026.02.001.
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Ethnography, ritual & cosmology

05 · 10 sources
Bonhomme, J. (2005) Le miroir et le crâne: parcours initiatique du Bwete Misoko (Gabon). Paris: CNRS Éditions.
Misoko initiation
Fernandez, J.W. (1972) ‘Tabernanthe iboga: narcotic ecstasis and the work of the ancestors’, in Furst, P.T. (ed.) Flesh of the Gods. New York: Praeger, pp. 237–260.
ethnography
Fernandez, J.W. (1982) Bwiti: An Ethnography of the Religious Imagination in Africa. Princeton, NJ: Princeton University Press. Available at: JSTOR.
foundational ethnography
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Fernandez, J.W. and Fernandez, R.L. (2001) ‘“Returning to the path”: the use of iboga[ine] in an equatorial African ritual context and the binding of time, space, and social relationships’, The Alkaloids: Chemistry and Biology, 56, pp. 235–247. Available at: https://doi.org/10.1016/S0099-9598(01)56017-4.
DOI checked
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Maas, U. and Strubelt, S. (2003) Music in the Iboga Initiation Ceremony in Gabon: Polyrhythms Supporting a Pharmacotherapy. Berlin: VWB.
music / ceremony
Mary, A. (1983) La naissance à l’envers: essai sur le rituel du Bwiti fang au Gabon. Paris: L’Harmattan.
Fang ritual
Raponda-Walker, A. and Sillans, R. (1962) Rites et croyances des peuples du Gabon. Paris: Présence Africaine.
regional ethnography
Samorini, G. (2024b) ‘Studies on the iboga cults. III. Iboga and Bwiti mythology’, Antrocom Online Journal of Anthropology, 20(2). Available at: antrocom.net.
open article
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Samorini, G. (2025a) ‘Studies on the iboga cults VII: the traditional Bwiti’, Antrocom Online Journal of Anthropology, 21(2).
comparative synthesis
The Metropolitan Museum of Art (2026) ‘Ngombi (arched harp), Fang/Kele peoples, Gabon, object 89.4.3527’. Available at: metmuseum.org (Accessed: 7 August 2026).
material culture
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Law, policy & patents

06 · 9 sources
CITES (2026) ‘Appendices I, II and III’. Available at: cites.org (Accessed: 7 August 2026).
current list
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Convention on Biological Diversity (CBD) (2026) ‘Access and Benefit-Sharing Clearing-House: Gabon’. Available at: absch.cbd.int (Accessed: 7 August 2026).
Nagoya implementation
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Drug Enforcement Administration (DEA) (2025) ‘Broomfield man sentenced to 48 months for ibogaine distribution’, 25 September. Available at: dea.gov.
current US status
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Ermakova, A.O. et al. (2025) ‘Of shrub, cactus, vine and toad: psychedelic species conservation and sustainability’, Frontiers in Conservation Science, 6, 1569528. Available at: https://doi.org/10.3389/fcosc.2025.1569528.
Verified
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ICEERS (2026) Charting a Path Forward for Iboga: Phase 3 Report. Barcelona: International Center for Ethnobotanical Education, Research and Service.
participatory policy report
International Narcotics Control Board (INCB) (2026) Green List: List of Psychotropic Substances under International Control. Vienna: United Nations.
treaty schedule
INTERPOL (2023) Illicit Trafficking of Natural Psychotropics. Lyon: INTERPOL.
official analytical report
Lotsof, H.S. (1985) ‘Rapid method for interrupting the narcotic addiction syndrome’, US Patent US4499096A, granted 12 February. Available at: Google Patents (Accessed: 29 July 2026).
The White House (2026) ‘Accelerating medical treatments for serious mental illness’, Executive Order 14401, 17 April. Available at: whitehouse.gov (Accessed: 29 July 2026).
primary policy
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Visionary phenomenology

07 · 3 sources
Kohek, M., Ohren, M., Hornby, P., Alcázar-Córcoles, M.Á. and Bouso, J.C. (2020) ‘The ibogaine experience: a qualitative study on the acute subjective effects of ibogaine’, Anthropology of Consciousness, 31(1), pp. 91–119. Available at: https://doi.org/10.1111/anoc.12119.
DOI checked
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Olash, C., Pahngur, M., Evans, L.K. et al. (2026) ‘Accelerated recovery using magnesium ibogaine: characterizing the subjective experience of its rapid healing from neuropsychiatric disorders’, npj Mental Health Research, 5, 8. Available at: https://doi.org/10.1038/s44184-026-00185-7.
DOI checked
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Rodríguez-Cano, B.J. et al. (2023) ‘Underground ibogaine use for the treatment of substance use disorders: a qualitative analysis of subjective experiences’, Drug and Alcohol Review, 42(2), pp. 401–414. Available at: https://doi.org/10.1111/dar.13587.
DOI checked
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Cross-correlations

Bwiti–Iboga ComplexCeremonial complex page: institutions, initiation, healing cults, regional branches, music and contemporary transformation. PRIMARY CULTURAL COMPLEX
Voacanga africanaRelated Apocynaceae tree containing voacangine; an important semisynthetic source for ibogaine chemistry but not a botanical substitute for iboga’s Gabonese ritual history. CHEMICAL / SUPPLY RELATION
Rauvolfia vomitoriaWest-central African medicinal relative containing different indole-alkaloid ensembles; shared family chemistry does not imply shared sacramental use. PHYTOCHEMICAL RELATIVE
Clinical Psychedelic RitualModern clinics, monitoring, psychometrics and integration constitute a distinct institutional complex around purified ibogaine and analogues. CONTEMPORARY TRANSLATION
Tabernanthe ellipticaThe other species retained in Vonk’s revision of the genus; not interchangeable with T. iboga in pharmacognosy or ethnographic attribution. TAXONOMIC SIBLING