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Yopo (Anadenanthera peregrina): the cohoba tree, its history and its chemistry
Topic: DMT
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Yopo is Anadenanthera peregrina, a tree of the Caribbean and tropical South America whose seeds were the source of a ritual snuff called cohoba by the Taíno and yopo by peoples of the Orinoco. Chemical analyses of its seeds most often report bufotenine as the main tryptamine, with DMT, and in some samples 5-MeO-DMT, also reported. Bufotenine has well-described effects on the heart and blood vessels. In Canada, DMT is in Schedule III of the Controlled Drugs and Substances Act; bufotenine, 5-MeO-DMT and the tree itself are not named.
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Yopo is a tree before it is anything else. It is a legume related to acacias and mimosas, and its seeds have a long, documented place in the ritual life of Indigenous peoples of northern South America and, before the colonial era, the Caribbean. This guide covers the plant, its names, the historical and ethnographic record, and what chemists have reported finding in it.
Education only, not guidance
This article describes botany, history, published chemistry and law. It gives no amounts, preparation, sourcing or instructions, and it describes traditional use only as recorded history. Nothing here is a recommendation. Evidence labels used below: established (shown in peer-reviewed or primary sources and not seriously disputed), preliminary (early, small or indirect) and unresolved (an open question).
What is yopo?
Yopo is the common name of *Anadenanthera peregrina* (L.) Speg., a shrub or tree in the pea family, Fabaceae. Plants of the World Online, run by the Royal Botanic Gardens, Kew, accepts the name and says the species grows mainly in the seasonally dry tropical biome. Its native range runs from the Caribbean to southern tropical America: Bolivia, northern, northeastern and southeastern Brazil, Colombia, the Dominican Republic, French Guiana, Guyana, Haiti, the Leeward Islands, Puerto Rico, Suriname, Trinidad and Tobago, Venezuela and the Windward Islands (POWO). Evidence: established.
The tree has carried many scientific names. Linnaeus first described it in 1753 as *Mimosa peregrina*; it was later placed in *Acacia*, *Niopa* and *Piptadenia*, and older chemistry papers call it *Piptadenia peregrina*. One synonym, *Inga niopo*, preserves the name niopo that Humboldt and Bonpland recorded (POWO). Much of the research below was published under the old names. Evidence: established.
A 2024 review describes the genus’s pods as long and flat, holding thin, flat, round and shiny brown or black seeds (Lema, 2024). The same review notes that *A. peregrina* was introduced to the Greater Antilles in pre-Hispanic times, while Kew lists the Caribbean islands as part of its native range (POWO). A 1994 review also describes the species as probably naturalized in the West Indies (Chamakura, 1994). Whether people carried the tree to the islands is still open. Evidence: unresolved.
Yopo, cohoba, cebil and vilca: which plant is which?
The genus *Anadenanthera* has two species, and their names are often mixed up online. *A. peregrina* is known as yopo, parica or cohoba, and is found in Colombia, Venezuela, Guyana, Brazil and Paraguay. Its relative *A. colubrina* is known as vilca or willka in Peru, Bolivia and Chile, and as cebil in Argentina, and grows mainly in seasonally dry forests between 0 and 30 degrees south (Lema, 2024). A 2022 research synthesis draws the same line: snuffs called cohoba and yopo come from *A. peregrina* in northern South America, and those called vilca, huilca and cibil from *A. colubrina* further south (Ermakova et al., 2022). Evidence: established.
| Anadenanthera peregrina | Anadenanthera colubrina | |
|---|---|---|
| Common names | Yopo, cohoba, parica, niopo | Vilca or willka (Peru, Bolivia, Chile); cebil (Argentina) |
| Where it grows | Caribbean to southern tropical America (Kew); northern South America | Seasonally dry forests between 0 and 30 degrees south |
| Best-known record | Taíno cohoba in the Caribbean; yopo among Orinoco peoples | Andean archaeology: snuff tubes, trays and pouches |
Most of the archaeology people quote as “ancient DMT” concerns *A. colubrina*, vilca, in the Andes. We cover those finds, from Chavín de Huántar to a Bolivian ritual bundle, in ancient DMT and snuff archaeology, and do not repeat them here.
What do early colonial sources say about cohoba?
The first written account of cohoba comes from Ramón Pané, who travelled with Columbus on his second voyage and described its ceremonial use in Hispaniola as early as 1496. In his account the snuff was used by priests to communicate with spirits. Many early writers then confused cohoba with tobacco snuff, and it was only in 1916 that the botanist W. E. Safford identified its source as *Piptadenia peregrina*, now *Anadenanthera peregrina* (Chamakura, 1994). Evidence: established for the record; the colonial accounts are written by outsiders and carry their biases.
Archaeology in the Caribbean has since added physical evidence. In 2014, researchers reported starch grains consistent with those in modern cojoba (*A. peregrina*) seeds on a coral milling base from a small precolonial habitation site in eastern Puerto Rico, in a context dated to about AD 1150–1250. It was the first such find in the West Indies. The authors propose that the seeds were used there mainly to help a healer divine the cause of illness (Pagán-Jiménez and Carlson, 2014). Evidence: the starch identification is established; the healing interpretation is the authors’, and preliminary.

Use of the snuff in the islands did not survive the colonial period. The ethnobotanist Richard Evans Schultes wrote in 1976 that it disappeared with the destruction of the Indigenous populations of the West Indies (Chamakura, 1994). That loss is part of the history, and it is a reason to treat surviving traditions on the mainland with care.
How is yopo recorded among Orinoco peoples?
On the mainland, European descriptions of niopo or yopo go back to Alexander von Humboldt and Aimé Bonpland, who recorded it among peoples of the Orinoco region of Colombia and Venezuela in 1801, and to the British botanist Richard Spruce, who described it in 1851 (Chamakura, 1994). A 2007 review in a Spanish neurology journal states that *Anadenanthera* snuff is still used by several Indigenous groups of the Orinoco basin, where it is known as yopo, and in the Brazilian and Colombian Amazon (Carod-Artal and Vázquez Cabrera, 2007). Evidence: established.
Modern ethnography shows the practice as living culture, not a relic. A 2011 study of the Piaroa and Cuiva of the Orinoco found that yopo is tied to the performance of narratives central to each group’s cosmology and identity. For the Cuiva, it is also a way of resisting persecution. Among the Piaroa, attitudes are shaped by shamanic ethics and by missionary activity: some lay people see yopo as a relic of the past, while shamans regard it as necessary to their work (Rodd and Sumabila, 2011). Evidence: established for these two communities; it does not describe every group that uses yopo.
What chemicals have analyses found in yopo?
The short version: bufotenine (5-hydroxy-DMT) is the compound most consistently reported in the seeds, DMT turns up as a minor or variable compound, and 5-MeO-DMT appears in some samples and in the bark. A 2024 review sums up the genus this way: the effects are attributed mainly to DMT, bufotenine and 5-MeO-DMT, particularly in the seeds (Lema, 2024). A 2020 toxicology review adds that DMT is a minor alkaloid in the bark, pods and beans of both *Anadenanthera* species (Malaca et al., 2020). Evidence: established that all three have been reported; the proportions vary widely.
The individual studies tell a more interesting story. Bufotenine was first isolated from the plant’s seeds in 1954, in material from Puerto Rico (Stromberg, 1954). A 1963 paper reported N-methyltryptamine, 5-methoxy-N-methyltryptamine and 5-MeO-DMT from the bark, not the seeds (Legler and Tschesche, 1963). The table below lists what each analysis reported, as summarised in a 1994 forensic review that read the originals (Chamakura, 1994).
| Year | Study | Material | What was reported |
|---|---|---|---|
| 1954 | Stromberg | Seeds from Puerto Rico | Bufotenine isolated: the first report from this plant (title of the paper and Chamakura) |
| 1955 | Fish, Johnson and Horning | Seeds and pods | Seeds: bufotenine, bufotenine oxide and DMT oxide. Pods: DMT |
| 1963 | Legler and Tschesche | Bark | N-methyltryptamine, 5-methoxy-N-methyltryptamine and 5-MeO-DMT (title of the paper); Chamakura adds that DMT was also found in the bark |
| 1967 | Holmstedt and Lindgren | Seeds from Puerto Rico and from western Brazil | Puerto Rico seeds: bufotenine as the main compound. Western Brazil seeds: 5-MeO-DMT as the main compound. DMT a minor compound in both |
| 1977 | Schultes and colleagues | Seeds collected by Spruce in 1854 | Only bufotenine, about 120 years after collection |
| 1977 | Schultes and colleagues | Fresh seeds from Puerto Rico, then the same seeds two years later | At first bufotenine, DMT, 5-MeO-DMT and a trace beta-carboline, in a ratio of about 80:19:1; two years later, only bufotenine |
Two lessons come out of that record. First, origin matters: the same species gave a bufotenine-dominant result from Puerto Rico and a 5-MeO-DMT-dominant result from western Brazil in the same 1967 study. Second, storage matters: the 1977 team saw the minor alkaloids disappear from stored seeds and stressed that storage time, plant part, soil, season and climate all need recording when seeds are analysed (Chamakura, 1994). Evidence: established for the reported results; they are a handful of samples, not a survey of the species.
So is yopo a “DMT plant”? Chemically, it is better described as a bufotenine plant in which DMT and sometimes 5-MeO-DMT also occur. For how these molecules differ, see what is bufotenin and 5-MeO-DMT vs DMT; for DMT across the natural world, see where DMT comes from in nature.
What does research report about yopo’s effects and risks?
The historical accounts are dramatic. Pané wrote that the snuff was so strong that people lost consciousness, and a priest, José Gumilla, writing in 1741, described yupa as driving people out of their minds. Humboldt attributed its stimulating effect to the lime mixed with it, which later writers called an error (Chamakura, 1994). These are outsiders’ descriptions, and they say little about what participants experienced or valued. Evidence: historical record, not clinical data.
The laboratory record centres on bufotenine, and much of it is about the body rather than the mind. The 1994 review quotes a 1950s remark by Dr. Isbell, a researcher of tryptamines, describing bufotenine as having powerful and dangerous effects on the heart and circulation: high blood pressure, a heart-rhythm disturbance in which the upper chambers stop beating, and a striking blue or purple colour of the upper body. It also summarises a 1956 injection study by Fabing and Hawkins in which volunteers developed chest tightness and a purple facial colour (Chamakura, 1994). Doses are not reproduced here. Evidence: established that these effects were reported in early studies; the studies were small and old.
Newer work points the same way. In a 2023 laboratory study, bufotenin increased the force and rate of heart-muscle contraction in mouse hearts engineered to carry the human serotonin 5-HT4 receptor, and increased the contraction force of isolated human atrial tissue (Neumann et al., 2023). That is tissue in a dish, not people, but it gives a mechanism for the cardiovascular effects described decades ago. Evidence: preliminary.
Whether bufotenine itself is psychedelic is still argued. The 1994 review collects both sides: a 1950s study by Turner and Merlis that could not produce intoxication in volunteers with snuff powders at amounts they tolerated, a reference text ranking bufotenine as having weak if any hallucinogenic potential, and the view that it does not easily cross from the blood into the brain (Chamakura, 1994). Our bufotenin explainer goes through that debate. Evidence: unresolved.
Why the chemistry makes risk hard to predict
The analyses above show that seeds of one species can differ in which compound dominates, and that their chemistry changes in storage. Bufotenine acts on the heart and blood vessels. Nobody can tell what a given sample contains by looking at it. This is a description of published findings, not advice about any substance.
If someone is in danger
Call 911 for immediate danger or urgent medical help, including if someone is unconscious, not breathing or having a seizure. In Ontario, the Ontario Poison Centre is at 1-800-268-9017; every province has a poison centre, listed by SickKids (AboutKidsHealth). If you or someone you know is thinking about suicide, call or text 9-8-8, 24 hours a day (Government of Canada). See also our safety page and how to help someone having a bad trip.
Why cultural respect matters here
Yopo is not a curiosity from the past. It remains part of the religious and social life of Indigenous peoples in the Orinoco region, under pressure from persecution and missionary activity (Rodd and Sumabila, 2011). A botanist writing about Amazonian poisons and narcotics argued that this kind of knowledge should be documented before it is lost, and that any commercial gain from it should directly benefit the peoples who hold it, under the rules of the Convention on Biological Diversity (Prance, 1999).

In practice, that means learning about yopo from the people who use it and the researchers who work with them, not from marketing that strips the plant of its context. The tree matters in other ways too: Kew records environmental and social uses as well as its use as a poison and a medicine (POWO).
Is yopo legal in Canada?
We read the Controlled Drugs and Substances Act on 24 October 2026, in the consolidation current to 30 September 2026 and last amended on 18 July 2026. Schedule III, item 7, lists “N,N-Dimethyltryptamine (DMT) (3-[(2-dimethylamino) ethyl]indole) and any salt thereof”. A search of the full text found no mention of bufotenine, of 5-MeO-DMT, of *Anadenanthera* or of *Piptadenia* (Justice Laws, CDSA). In other words, one of the compounds reported in the seeds is a Schedule III substance, while the plant itself and the other two compounds are not named in the Act. Evidence: established for what the text says.
Not being named in the Act does not make a substance legal to sell, import or consume, and other federal laws can apply. Laws also change. For the full picture on DMT, see is DMT legal in Canada. This is not legal advice.
What we still don’t know
- Whether yopo is native to the Caribbean islands or was carried there by people before European contact (unresolved).
- How much the chemistry of the seeds varies across the species’ range: the published analyses cover only a few samples (unresolved).
- How much of the reported effects come from bufotenine, from DMT or 5-MeO-DMT, or from other plants and additives used in traditional snuffs (unresolved).
- What cohoba meant to the Taíno in their own terms: the written record comes from colonial outsiders (unresolved).
- We did not read the 1954, 1955, 1967 and 1977 chemistry papers in full; their findings here come from a 1994 review that did.
Common questions
What is yopo?
Yopo is the common name of Anadenanthera peregrina, a tree in the pea family native from the Caribbean to tropical South America. Its seeds were the source of a ritual snuff recorded among the Taíno as cohoba and among Orinoco peoples as yopo.
What is the difference between yopo and cebil or vilca?
They are two species of the same genus. Yopo is Anadenanthera peregrina, found mainly in northern South America and the Caribbean. Cebil and vilca are names for Anadenanthera colubrina, which grows further south, in Argentina, Bolivia, Peru and Chile, and is the species most often found in Andean archaeology.
What is cohoba?
Cohoba was the Taíno name for a ritual snuff described in Hispaniola by Ramón Pané in the 1490s. In 1916 the botanist W. E. Safford identified its source as the tree now called Anadenanthera peregrina. Its use in the islands did not survive the colonial period.
Does yopo contain DMT?
Analyses have reported DMT in the seeds, pods and bark, usually as a minor compound. Bufotenine is the compound most consistently reported in the seeds, and some samples and the bark also contained 5-MeO-DMT. The mix varied with where the seeds came from and how long they were stored.
Is bufotenine dangerous?
Early human studies and expert accounts describe strong effects on the heart and circulation, including high blood pressure, heart-rhythm disturbance and a purple colouring of the face and upper body. A 2023 lab study found it increases heart-muscle contraction through the 5-HT4 receptor. Whether it is psychedelic is still debated.
Is yopo legal in Canada?
As read on 24 October 2026, the Controlled Drugs and Substances Act lists DMT in Schedule III. It does not name Anadenanthera peregrina, bufotenine or 5-MeO-DMT. Not being named does not mean legal to sell or safe, and laws change. This is not legal advice.
Shroomverse sells mushroom products. This article is general information about the botany, history, chemistry and legal status of a South American tree. It is not medical, legal or purchasing advice, and it does not recommend any product.
SOURCES
- Anadenanthera peregrina (L.) Speg., Plants of the World Online, Royal Botanic Gardens, Kew. Accessed . Page read in a browser. Supports the accepted name, first publication 1923, shrub or tree of the seasonally dry tropical biome, native range Caribbean to southern tropical America with the listed countries, introduced to St Helena, synonyms (Mimosa peregrina L. 1753, Piptadenia peregrina, Niopa peregrina, Inga niopo and others), and environmental, social, poison and medicine uses.
- Contemporary Uses of Vilca (Anadenanthera colubrina var. cebil): A Major Ritual Plant in the Andes (Lema VS, Plants 13(17):2398, 2024), MDPI (peer-reviewed, open access); full text via Europe PMC, PMC11397254. Accessed . Introduction read in full text. Supports the pod and seed description, the A. colubrina names (vilca, willka, cebil) and range (seasonally dry forests, 0–30 degrees south), A. peregrina names (yopo, parica, cohoba) and countries, its pre-Hispanic introduction to the Greater Antilles, and DMT, bufotenin and 5-MeO-DMT as the genus’s main psychoactive compounds, particularly in seeds. Preparation descriptions deliberately not reproduced.
- A narrative synthesis of research with 5-MeO-DMT (Ermakova AO, Dunbar F, Rucker J, Johnson MW; Journal of Psychopharmacology, 2022), SAGE (peer-reviewed); full text via Europe PMC, PMC8902691. Accessed . ‘Traditional use’ section read. Supports cohoba and yopo snuffs from A. peregrina in northern South America, documented use as far as the West Indies, and vilca, huilca and cibil from A. colubrina in central and southern South America.
- Bufotenine: a hallucinogen in ancient snuff powders of South America and a drug of abuse on the streets of New York City (Chamakura RP, Forensic Science Review 6(1), 1994), Forensic Science Review; PDF from the MAPS Psychedelic Bibliography. Accessed . Full text read. Supports Pané’s 1496 account and use to communicate with spirits; Safford’s 1916 identification; Humboldt and Bonpland (1801) and Spruce (1851); Schultes 1976 on disappearance in the West Indies; ‘probably naturalized’ in the West Indies; the chemistry summaries of Stromberg 1954, Fish et al. 1955, bark analyses, Holmstedt and Lindgren 1967 and Schultes et al. 1977 (storage); Isbell’s description of cardiovascular effects; Fabing and Hawkins 1956; Turner and Merlis; the reference-text ranking; the blood-brain barrier view. Doses, concentrations and preparation details in the review deliberately not reproduced.
- Recent Archaeobotanical Findings of the Hallucinogenic Snuff Cojoba (Anadenanthera peregrina (L.) Speg.) in Precolonial Puerto Rico (Pagán-Jiménez JR, Carlson LA; Latin American Antiquity 25(1):101–116, 2014), Society for American Archaeology (peer-reviewed). Accessed . Abstract read via Crossref. Supports starch grains consistent with cojoba seeds on a coral milling base from a small precolonial site in eastern Puerto Rico, context dated AD 1150–1250, first such find in the West Indies, and the authors’ proposal of use by a healer for divination of illness. The paper’s experimental processing work deliberately not described.
- Yopo, ethnicity and social change: a comparative analysis of Piaroa and Cuiva yopo use (Rodd R, Sumabila A; Journal of Psychoactive Drugs, 2011), Taylor & Francis (peer-reviewed). Accessed . Abstract read via Europe PMC. Supports yopo use by most Orinocoan groups including the Cuiva and Piaroa, its link to cosmology and identity, Cuiva use as resistance to persecution, and the influence of shamanic ethics and missionary activity on Piaroa attitudes.
- [Ritual use of Anadenanthera seeds among South America natives] (Carod-Artal FJ, Vázquez Cabrera CB; Neurología, 2007), Elsevier España (peer-reviewed); record and English abstract via Europe PMC, PMID 17610173. Accessed . Abstract read via Europe PMC. Supports present-day use of Anadenanthera by several native groups in the Orinoco basin, where it is known as yopo, and in the Brazilian and Colombian Amazon. Its preparation sentence deliberately not reproduced.
- The Isolation of Bufotenine from Piptadenia peregrina (Stromberg VL; Journal of the American Chemical Society 76(6):1707, 1954), American Chemical Society. Accessed . Bibliographic record checked on Crossref; the publisher page was not accessible to us. Cited for its title and date; Puerto Rico origin of the seeds from Chamakura (1994).
- Die Isolierung von N-Methyltryptamin, 5-Methoxy-N-methyltryptamin und 5-Methoxy-N,N-dimethyltryptamin aus der Rinde von Piptadenia peregrina Benth (Legler G, Tschesche R; Die Naturwissenschaften 50(3):94–95, 1963), Springer. Accessed . Bibliographic record checked on Crossref (no abstract). Cited only for what its title states: isolation of N-methyltryptamine, 5-methoxy-N-methyltryptamine and 5-MeO-DMT from the bark.
- Toxicology and Analysis of Psychoactive Tryptamines (Malaca S, Lo Faro AF, Tamborra A, Pichini S, Busardò FP, Huestis MA; International Journal of Molecular Sciences 21(23):9279, 2020), MDPI (peer-reviewed, open access); full text via Europe PMC, PMC7730282. Accessed . Full text searched. Supports DMT as a minor alkaloid in the bark, pods and beans of A. peregrina and A. colubrina.
- Cardiovascular effects of bufotenin on human 5-HT4 serotonin receptors in cardiac preparations of transgenic mice and in human atrial preparations (Neumann J et al., Naunyn-Schmiedeberg’s Archives of Pharmacology, 2023), Springer (peer-reviewed); abstract via Europe PMC, PMC10244282. Accessed . Abstract read. Bufotenin increased force of contraction and beating rate in hearts from mice expressing the human 5-HT4 receptor (not in wild-type hearts) and increased force of contraction in isolated human atrial preparations. Concentrations not reproduced.
- The poisons and narcotics of the Amazonian Indians (Prance G, Journal of the Royal College of Physicians of London, 1999), Royal College of Physicians; full text via PubMed Central, PMC9665745. Accessed . Abstract read via Europe PMC. Supports the need to document Indigenous plant knowledge before it is lost and that commercial gain should directly benefit the peoples concerned under the Convention on Biological Diversity.
- Controlled Drugs and Substances Act (S.C. 1996, c. 19), full text, Justice Laws Website, Government of Canada. Accessed . Consolidation current to 2026-09-30, last amended 2026-07-18, read 24 October 2026. Schedule III item 7 quoted (DMT and any salt thereof). The full text was searched for ‘bufot’, ‘5-methoxy’, ‘tryptamine’, ‘Anadenanthera’ and ‘Piptadenia’: no match for bufotenine, 5-MeO-DMT or either plant name; the only tryptamines named are DET, DMT and etryptamine.
- Get help with mental health, Government of Canada. Accessed . Page read 24 October 2026 (page details dated 2026-01-14). Supports calling 9-1-1 in immediate danger or for urgent medical support, and calling or texting 9-8-8, 24 hours a day, 7 days a week.
- Poison information centres in Canada, AboutKidsHealth, The Hospital for Sick Children (SickKids). Accessed . Page read 24 October 2026. Supports the Ontario Poison Centre toll-free number 1-800-268-9017, the provincial list, and calling 911 if someone is unconscious, not breathing or having a seizure.
CHANGES
- : Published. All sources opened and checked on this date, including the Kew species record and the CDSA consolidation current to 30 September 2026. Older chemistry papers reported through a 1994 review, as stated in the table.



