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The following is a list of plants known to contain tryptamines.
The following is a list of plants known to contain tryptamines.
{{:Mimosa hostilis}}


=== Acacia ===
=== Acacia ===
{{:Acacia_acuminata}}
[[Acacia_acuminata]]
 
{{:Acacia_alpina}}
 
{{:Acacia angustifolia}}


{{:Acacia angustissima}}
[[Acacia_alpina]]


{{:Acacia auriculiformis}}
[[Acacia angustifolia]]


{{:Acacia baileyana}}
[[Acacia angustissima]]


{{:Acacia berlandieri}}
[[Acacia auriculiformis]]


{{:Acacia catechu}}
[[Acacia baileyana]]


{{:Acacia caven}}
[[Acacia berlandieri]]


{{:Acacia colei}}
[[Acacia catechu]]


{{:Acacia complanata}}
[[Acacia caven]]


{{:Acacia constricta}}
[[Acacia colei]]


{{:Acacia confusa}}
[[Acacia complanata]]


{{:Acacia cornigera}}
[[Acacia constricta]]


{{:Acacia cultriformis}}
[[Acacia confusa]]


{{:Acacia farnesiana}}
[[Acacia cornigera]]


{{:Acacia filiciana}}
[[Acacia cultriformis]]


{{:Acacia_floribunda}}
[[Acacia farnesiana]]


{{botanics_info|image:NoImage.png|Acacia georginae|
[[Acacia filiciana]]
* Psychoactive,[8] plus deadly toxins
}}


{{botanics_info|image:NoImage.png|Acacia greggii|
[[Acacia_floribunda]]
* N-methyl-β-phenethylamine,[12] phenethylamine[36]
}}


{{botanics_info|image:NoImage.png|Acacia harpophylla|
[[Acacia laeta]]
* Phenethylamine, hordenine at a ratio of 2:3 in dried leaves, 0.6% total[6]
}}
 
{{botanics_info|image:NoImage.png|Acacia holoserica|
* Hordenine, 1.2% in bark[6]
}}
 
{{botanics_info|image:NoImage.png|Acacia horrida|
* Psychoactive
}}
 
{{botanics_info|image:NoImage.png|Acacia implexa|
* Psychoactive
}}
 
{{botanics_info|image:NoImage.png|Acacia karroo|
* Psychoactive
}}
 
{{botanics_info|image:NoImage.png|Acacia kempeana|
* Psychoactive
}}
 
{{botanics_info|image:NoImage.png|Acacia kettlewelliae|
* 1.5[6]–1.88%[38] alkaloids, 92% consisting of phenylethylamine.[6] 0.9% N-methyl-2-phenylethylamine found a different time
}}
 
{{botanics_info|image:NoImage.png|Acacia laeta|
* DMT in the leaf (Trout's Notes)
* DMT in the leaf (Trout's Notes)
}}
{{botanics_info|image:NoImage.png|Acacia lingulata|
* Psychoactive
}}


{{botanics_info|image:NoImage.png|Acacia longifolia|
[[Acacia longifolia]]
* 0.2% tryptamine in bark, leaves, some in flowers, phenylethylamine in flowers (Hegnauer 1994)
* 0.2% tryptamine in bark, leaves, some in flowers, phenylethylamine in flowers (Hegnauer 1994)
* DMT in plant (Lyceaum)
* DMT in plant (Lyceaum)
}}


{{botanics_info|image:NoImage.png|Acacia macradenia|
[[Acacia maidenii]]
* Tryptamine
}}
 
{{botanics_info|image:NoImage.png|Acacia maidenii|
* Bark of A. maidenii contains 0.6% of N-methyltryptamine and DMT in the proportions approx. 2:3 (Fitzgerald & Sioumis 1965)
* Bark of A. maidenii contains 0.6% of N-methyltryptamine and DMT in the proportions approx. 2:3 (Fitzgerald & Sioumis 1965)
}}


{{botanics_info|image:NoImage.png|Acacia mangium|
[[Acacia melanoxylon]]
* Psychoactive
* DMT in the bark and leaf, less than 0.02% total alkaloids (Hegnauer 1994)
}}


{{botanics_info|image:NoImage.png|Acacia melanoxylon|
* DMT in the bark and leaf, less than 0.02% total alkaloids (Hegnauer 1994)
}}


{{botanics_info|image:NoImage.png|Acacia mellifera|  
[[Acacia mellifera]]  
* DMT in the leaf (Trout's Notes)
* DMT in the leaf (Trout's Notes)
}}


{{botanics_info|image:NoImage.png|Acacia nilotica|
[[Acacia nilotica]]
* DMT in the leaf (Trout's Notes)
* DMT in the leaf (Trout's Notes)
}}


{{botanics_info|image:NoImage.png|Acacia obtusifolia|
[[Acacia obtusifolia]]
* 0.4 to 0.5 % DMT/NMT in the dried bark (Csiro 1990)
* 0.4 to 0.5 % DMT/NMT in the dried bark (Csiro 1990)
*0.15-0.6% DMT,NMT(2:1)plus trace betacarboline in bark, 0.06-0.2% leaves (Southern Cross University comissioned test 2001)
*0.15-0.6% DMT,NMT(2:1)plus trace betacarboline in bark, 0.06-0.2% leaves (Southern Cross University comissioned test 2001)
*5-MeoDMT & bufotenine in some loctations (E., Entheogen Review 1995-6; Trout's Notes 2005-10) Is not fast growing in the wild and is under threat of serious overharvesting. Is NOT considered a weed as previously stated here, and will become rarer if wild seed populations exploited further.(Nen, original bioassay subject)
*5-MeoDMT & bufotenine in some loctations (E., Entheogen Review 1995-6; Trout's Notes 2005-10) Is not fast growing in the wild and is under threat of serious overharvesting. Is NOT considered a weed as previously stated here, and will become rarer if wild seed populations exploited further.(Nen, original bioassay subject)
{{botanics_info|image:NoImage.png|Acacia oerfota|
 
[[Acacia oerfota]]
* Less than 0.1% DMT in leaf (Ott)
* Less than 0.1% DMT in leaf (Ott)
}}


{{botanics_info|image:NoImage.png|Acacia penninervis|
* Psychoactive
}}


{{botanics_info|image:NoImage.png|Acacia phlebophylla|
[[Acacia phlebophylla]]
* 0.3% DMT in leaf, NMT (Trout's Notes)
* 0.3% DMT in leaf, NMT (Trout's Notes)
}}
{{botanics_info|image:NoImage.png|Acacia platensis|
* Psychoactive
}}


{{botanics_info|image:NoImage.png|Acacia podalyriaefolia|
[[Acacia podalyriaefolia]]
* Tryptamine in the leaf (Trout's Notes)
* Tryptamine in the leaf (Trout's Notes)
* 0.5% to 2% DMT in fresh bark, phenethylamine trace amounts (Hegnauer 1994)
* 0.5% to 2% DMT in fresh bark, phenethylamine trace amounts (Hegnauer 1994)
}}


{{botanics_info|image:NoImage.png|Acacia polyacantha|
[[Acacia polyacantha]]
* DMT in leaf (Trout's Notes)
* DMT in leaf (Trout's Notes)
}}
{{botanics_info|image:NoImage.png|Acacia pycantha|
* Psychoactive,[8] but less than 0.02% total alkaloids
}}


{{botanics_info|image:NoImage.png|Acacia retinodes|
[[Acacia retinodes]]
* DMT and MMT (www.factorey.ch/Eins.htm)  
* DMT and MMT (www.factorey.ch/Eins.htm)  
* Less than 0.02% total alkaloids found (Hegnauer 1994)
* Less than 0.02% total alkaloids found (Hegnauer 1994)
}}


{{botanics_info|image:NoImage.png|Acacia roemeriana|
[[Acacia rigidula]]
* β-methyl-phenethylamine
}}
 
{{botanics_info|image:NoImage.png|Acacia rigidula|
* DMT, NMT, tryptamine, amphetamines, mescaline, nicotine and others (Phytochem. 199
* DMT, NMT, tryptamine, amphetamines, mescaline, nicotine and others (Phytochem. 199
}}


{{botanics_info|image:NoImage.png|Acacia salicina|
[[Acacia senegal]]
* Psychoactive[8][9] Ash used in Pituri.
* DMT, in the leaf
}}
 
{{botanics_info|image:NoImage.png|Acacia sassa|
* Psychoactive
}}
 
{{botanics_info|image:NoImage.png|Acacia schaffneri|
* β-methyl-phenethylamine, Phenethylamine[36] Amphetamines and mescaline also found
}}
 
{{botanics_info|image:NoImage.png|Acacia schottii|
* β-methyl-phenethylamine
}}


{{botanics_info|image:NoImage.png|Acacia senegal|
* DMT, in the leaf
}}


{{botanics_info|image:NoImage.png|Acacia simplex|
[[Acacia simplex]]
*DMT and NMT, in the leaf, stem and trunk bark, 0.81% DMT in bark, MMT
*DMT and NMT, in the leaf, stem and trunk bark, 0.81% DMT in bark, MMT
}}


{{botanics_info|image:NoImage.png|Acacia taxensis|
* β-methyl-phenethylamine
}}


{{botanics_info|image:NoImage.png|Acacia tenuifolia|
[[Acacia tortilis]]
* Psychoactive
}}
 
{{botanics_info|File:290px-Eat267.jpg|Acacia tortilis|
* DMT, NMT, and other tryptamines
* DMT, NMT, and other tryptamines
}}


{{botanics_info|image:NoImage.png|Acacia sieberiana|
[[Acacia sieberiana]]
* DMT in the leaf (Trout's Notes)
* DMT in the leaf (Trout's Notes)
}}
{{botanics_info|image:NoImage.png|Acacia verek|
* Psychoactive (Rätsch 2004)
}}


{{botanics_info|image:NoImage.png|Acacia vestita|
* Tryptamine, in the leaf and stem (Trout's Notes)
* Less than 0.02% total alkaloids (Hegnauer 1994)
}}


=== Anadenanthera ===
=== Anadenanthera ===

Revision as of 17:46, 4 November 2011

http://wiki.dmt-nexus.me/Category:Alkaloids

Brief overview - What is DMT?

NN-Dimethyltryptamine or DMT for short is an short acting psychedelic entheogen which allows a persons consciousness to voyage into the most incredible dimensions, visions, thoughts and experiences imaginable.

It is without doubt one of the most powerful yet mysterious psychedelics in existence but to classify DMT as merely a drug would be doing it a great injustice as DMT is more a trans dimensional key into places and vistas so profound and awe inspiring that it raises many new questions regarding the nature of reality and our place within it.

DMT exists naturally in every human being and also throughout the plant and animal kingdoms. It occurs naturally in many mammals, marine animals, trees, grasses, flowers and shoots.

DMT is closely related to serotonin, the naturally occurring neurotransmitter that psychedelics affect so widely. The pharmacology of DMT is similar to that of other well-known psychedelics. It affects receptor sites for serotonin in much the same way that LSD, psilocybin, and mescaline do. These serotonin receptors are widespread throughout the body and can be found in blood vessels, muscle, glands, and skin.

There are a number of ways to acquire this entheogen. The first and most difficult way is to have some substantial chemistry knowledge and experience and actually synthesize pure DMT in a laboratory. This a rather tricky and time consuming process and requires access to some rather obscure and hard to acquire chemicals.

The most common and easiest method to acquire DMT is to extract it from the various plant species that contain the compound. The various plants and extraction techniques can be found on this wiki at the extraction teks.

Chemical and physical properties

DMT = N,N-Dimethyltryptamine

Freebase DMT

  • Appearance: White/Transparent crystals
  • CAS Registry Number: 61-50-7
  • Composition: C12H16N2
  • Molecular Weight: 188.26884 g/mol
  • Melting point: 44-68°C (Conflicting reports in literature, as mentioned in TIHKAL)
  • Boiling point: Theoretically 360-380°C
  • XLogP: 2.0
  • XLogP3: 2.5 (PubChem)
  • pKa: 8.68 (Merck Index)
  • Colorimetric reagent results: Here
  • Stability/Degradation: Oxidation to DMT N-Oxide (yellow oil) in extended presence of oxygen (specialy in evaporation of dmt-containing solvents with heat and/or fan or generally in prolonged exposure to open air). N-oxide may be reverted back to the parent compound by reduction, as described in the N-Oxide to Freebase Wiki.
  • Solubility:

Very Soluble in Xylene, Toluene, Limonene, acetone, Isopropyl Alcohol (IPA), methanol, ethanol, Dichloromethane (DCM), chloroform, ether, Butanone (also known as methyl ethyl ketone (MEK)) and butanol.

Soluble in naphtha, hexane, heptane but almost insoluble in these solvents at freezing temperatures

Almost insoluble in water.

DMT N-Oxide

  • Appearance: Yellow oil
  • XLogP3: 2
  • Colorimetric reagent results: Here
  • Solubility:

Soluble in Xylene, Toluene, Limonene

Slightly soluble in basic water

Insoluble in naphtha

DMT Fumarate

  • Molecular Weight: 492.608 g/mol
  • Solubility:

Very soluble in water

Soluble in methanol (~10mg/ml)

Soluble in boiling IPA, Practically insoluble in room temp IPA (~1mg/ml), Insoluble in freeze-cold IPA.

Slightly soluble in ethanol (~5mg/ml)

Insoluble in cold acetone

Insoluble in FASI (Fumaric Acid Saturated IPA)

Insoluble in FASA (Fumaric Acid Saturated Acetone)


Effects

Depending on the dosage, the effects of DMT can range from a multitude of sensations, from bizarre, beautiful and even 'impossible' visions to literally jaw hanging awe as one is propelled into other dimensions of existence where human language and logic cannot even begin to describe or comprehend.

There have been a few attempts to define different levels and types of experience. Psychedelic Monographs and Essays[1] discusses different levels of a DMT experience.

The Hyperspace Lexicon project is an attempt to create a new vocabulary to try to describe the DMT realm

Pharmacology, toxicity and general safety

For info on DMT safety, please reffer to Health and Safety section

Plants containing DMT

The following is a list of plants known to contain tryptamines.

Mimosa hostilis
Mimosa hostilis seed pod
Mimosa hostilis flower



General Plant Info

Mimosa hostilis is the former scientific name for Mimosa tenuiflora, and the two names are synonymous [2][3]. The older name is still widely know due to its presence in the literature and as distributers of botanical products still use the older term. M. tenuiflora is an entheogen known as Jurema, Jurema Preta, Black Jurema, and Vinho de Jurema. Dried Mexican Mimosa Hostilis root bark has been recently shown to have a DMT content of about 1%. The stem bark has about 0.03% DMT.

To date no β-carbolines such as harmala alkaloids have been detected in Mimosa tenuiflora decoctions, however the isolation of a new compound called "Yuremamine" from Mimosa tenuiflora as reported in 2005 represents a new class of phyto-indoles [4]. This may explain the reported oral activity of DMT in Jurema without the addition of an MAOI. Imported MHRB typically requires the addition of an MAOI in the preparation of ayahuasca.


Identification

Alkaloid content

  • Root Bark contains DMT - 0.31% to 0.57% (Schultes 1977)
  • Inner root bark contains up to 2% active alkaloids (Extractions from DMT-Nexus and others)
  • 3% of the total alkaloids (or 0.04% of rootbark) is NMT and 2-Methyl-1,2,3,4-Tetrahydro-Beta-Carboline (Analysis of jungle spice, Analysis of red/yellow/white spices

Extraction teks

For extracting DMT , any of the extraction teks described here will work.

Yuremamine is sensitive to heat and pH changes so only cold water (or alcoholic) soak will retrieve it.

Cultivation

Growing: Mimosas aren´t cold proof. For outdoor growing they deserve a sunny place with leachy middle nutrient soil. Throughout the vegetation are copiously watered, in winter the watering is tied down on to the minimum. They are breeding with the seeds, but can be breeded with the cutting also.

Refinery for the Purpose of Extraction

Mimosa Hostilis Root Bark can be acquired in different stages of preparation. Usually it is sold as whole, shredded or pre-powdered root-bark, but one may have access to the whole root—usually when harvested directly.

  • The whole root must cleaned and stripped of its inner root-bark while discarding the rest of the root.
  • The whole root-bark must generally be torn by hand, cut, or smashed with a blunt object prior to shredding.
  • The shredded should be further broken down as much as possible by peeling/cutting/blending to increase surface area for alkaloids to be extracted.
  • The pre-powdered can always be used "as-is".

Below details how to break it from whole root

The Root

Note: Only the Inner Root Bark is necessary for extraction, the core and outer parts are to be discarded!


Root preparation

Pictured below is its original after being harvested from the plant. Notice the middle core is quite distinct from the root-bark, the outer bark is much more brown:


Cleaning the root

Cleaning The Root

The first step in refinery is to brush the outside to remove the dirt. Then the outer bark must be lightly scraped with a good knife. It is preferable to remove at least some of the outermost layer to uncover the more blackish and purplish layer underneath:


Peeling the Inner Root Bark

Peeling the Inner Root Bark

Once the outermost part has been removed, peel off the Inner Root Bark to separate it from the core. This can easily be accomplished immediately by hand, though the use of a knife may be helpful.

Here's the inner core which is to be discarded:


Result of root preparation

Result of root preparation

The peeled inner root-bark now needs to dry. This may be accomplished by simply leaving it in the sun. Here's how it should look:


Breaking the rootbark up

Breaking the rootbark up

The pieces/strips of inner root-bark require further refinery to expose a larger surface area and increase the availability of the alkaloids for extraction. If storage is desired, then the whole pieces are preferable, as the alkaloids are less exposed and thus better protected.

First strip the pieces further into thinner layers with the hands, then cut it up with good scissors into smaller squares, then break it down in small amounts and short/medium bursts with a blender or coffee grinder (to prevent breaking of blender/grinder)


References

  1. ↑ Psychedelic Monographs and Essays [1]
  2. ↑ USDA, ARS, National Genetic Resources Program. Germplasm Resources Information Network - (GRIN) [Online Database]. National Germplasm Resources Laboratory, Beltsville, Maryland. URL: http://www.ars-grin.gov/cgi-bin/npgs/html/taxon.pl?24430
  3. ↑ Lewis, G.P. (1987) Royal Botanic Gardens, Kew 369 pp Legumes of Bahia.
  4. ↑ Vepsäläinen, Jouko J.; Auriola, Seppo; Tukiainen, Mikko; Ropponen, Nina & Callaway, J.C. (2005). "Isolation and characterization of yuremamine, a new phytoindole". Planta Medica, 71: 1053-1057. URL: http://www.ncbi.nlm.nih.gov/pubmed/16320208

Links

Acacia

Acacia_acuminata

Acacia_alpina

Acacia angustifolia

Acacia angustissima

Acacia auriculiformis

Acacia baileyana

Acacia berlandieri

Acacia catechu

Acacia caven

Acacia colei

Acacia complanata

Acacia constricta

Acacia confusa

Acacia cornigera

Acacia cultriformis

Acacia farnesiana

Acacia filiciana

Acacia_floribunda

Acacia laeta

  • DMT in the leaf (Trout's Notes)

Acacia longifolia

  • 0.2% tryptamine in bark, leaves, some in flowers, phenylethylamine in flowers (Hegnauer 1994)
  • DMT in plant (Lyceaum)

Acacia maidenii

  • Bark of A. maidenii contains 0.6% of N-methyltryptamine and DMT in the proportions approx. 2:3 (Fitzgerald & Sioumis 1965)

Acacia melanoxylon

  • DMT in the bark and leaf, less than 0.02% total alkaloids (Hegnauer 1994)


Acacia mellifera

  • DMT in the leaf (Trout's Notes)

Acacia nilotica

  • DMT in the leaf (Trout's Notes)

Acacia obtusifolia

  • 0.4 to 0.5 % DMT/NMT in the dried bark (Csiro 1990)
  • 0.15-0.6% DMT,NMT(2:1)plus trace betacarboline in bark, 0.06-0.2% leaves (Southern Cross University comissioned test 2001)
  • 5-MeoDMT & bufotenine in some loctations (E., Entheogen Review 1995-6; Trout's Notes 2005-10) Is not fast growing in the wild and is under threat of serious overharvesting. Is NOT considered a weed as previously stated here, and will become rarer if wild seed populations exploited further.(Nen, original bioassay subject)

Acacia oerfota

  • Less than 0.1% DMT in leaf (Ott)


Acacia phlebophylla

  • 0.3% DMT in leaf, NMT (Trout's Notes)

Acacia podalyriaefolia

  • Tryptamine in the leaf (Trout's Notes)
  • 0.5% to 2% DMT in fresh bark, phenethylamine trace amounts (Hegnauer 1994)

Acacia polyacantha

  • DMT in leaf (Trout's Notes)

Acacia retinodes

  • DMT and MMT (www.factorey.ch/Eins.htm)
  • Less than 0.02% total alkaloids found (Hegnauer 1994)

Acacia rigidula

  • DMT, NMT, tryptamine, amphetamines, mescaline, nicotine and others (Phytochem. 199

Acacia senegal

  • DMT, in the leaf


Acacia simplex

  • DMT and NMT, in the leaf, stem and trunk bark, 0.81% DMT in bark, MMT


Acacia tortilis

  • DMT, NMT, and other tryptamines

Acacia sieberiana

  • DMT in the leaf (Trout's Notes)


Anadenanthera

 Anadenanthera colubrina
  • Seed pods contain dimethyltryptamine and the seeds bufotenin, bufotenin oxide, and oxide of dimethyltryptamine (GRANIER-DOYEUX 1965)
  • Leaves, Bark, and Seeds contain DMT, 5-MeO-DMT and related compounds (Schultes 1977)


Anadenanthera macrocarpa
  • Seed pods contain dimethyltryptamine and the seeds bufotenin, bufotenin oxide, and oxide of dimethyltryptamine (GRANIER-DOYEUX 1965)


Anadenanthera peregrina
Tryptamines known to be present in A. peregrina [1] Bufotenine (seeds)Bufotenine N-oxide (seeds)N,N-Dimethyltryptamine N-oxide (seeds)N,N-Dimethyltryptamine (bark)(pods)(seeds)5-Methoxy-N-methyltryptamine (bark)O-Methylbufotenine (bark) (seeds)N-Methyltryptamine (bark)


Common Reed

 Arundo donax
Entire Plant contains 5-MeO-DMT (Shulgin, TIHKAL)Flowers contain DMT, 5-MeO-DMT, and 5-MeO-NMT (Shulgin, TIHKAL)Roots contain DMT, 5-MeO-DMT, 5-MeO-NMT, Bufotenine, bufotenidine, dehydrobufotenidine (Shulgin, TIHKAL)


Desmanthus illinoensis
Root contains DMT - 0.200% (Ott)Root Bark contains DMT - 0.340% (Ott)


Phalaris arundinacea (Reed Canary Grass)
Leaves contain DMT, 5-MeO-DMT, and related compounds (Smith 1977) 0.0004-0.121% Total Alkaloids (Dried) Lycaeum (DMT, Life and the Universe)


Phalaris tuberosa
Leaves and seedlings contain DMT, 5-MeO-DMT, and related compounds (Smith 1977)DMT - 0.100% (erowid)5-MeO-DMT - 0.022% (erowid)5-OH-DMT - 0.005% (erowid)


Phragmites australis (Common Reed)
DMT in roots (Ott)


Delosperma

 Delosperma acuminatum
DMT, 5-MEO-DMT (Trout's Notes)


Delosperma cooperi
DMT, 5-MEO-DMT (Trout's Notes)


Delosperma ecklonis
DMT (Trout's Notes)


Delosperma esterhuyseniae
DMT (Trout's Notes)


Delosperma hallii
5-MEO-DMT (Trout's Notes)


Delosperma harazianum
DMT, 5-MEO-DMT (Trout's Notes)


Delosperma hirtum
DMT (Trout's Notes)


Delosperma lydenbergense
DMT, 5-MEO-DMT (Trout's Notes)


Delosperma nubigenum
5-MEO-DMT (Trout's Notes)


Delosperma pageanum
DMT, 5-MEO-DMT (Trout's Notes)


Delosperma pergamentaceum
Traces of DMT (Trout's Notes)


Delosperma tradescantioides
DMT (Trout's Notes)


Desmodium

 Desmodium caudatum
  • Roots: 0.087% DMT, Bufotenine-N-oxide 0.03% (Trout's Notes)


Desmodium gangeticum
  • DMT, 5-MEO-DMT, whole plant, roots, stems, leaves (Ott)


Desmodium gyrans
  • DMT, 5-MEO-DMT, leaves, roots (Ott)


Desmodium pulchellum
  • DMT, 5-MEO-DMT, whole plant, roots, stems, leaves, flowers (Ott)


Desmodium racemosum
  • 5-MEO-DMT (Ott)


Desmodium triflorum
  • DMT-N-oxide, roots (Ott)


Lespedeza bicolor
var. japonica
  • DMT, 5-MEO-DMT in leaves and root bark (Ott)


Petalostylis

 Petalostylis cassioides
0.4-0.5% tryptamine, DMT, etc. in leaves and stems (Johns et al 1966)


Mimosa

 Mimosa ophthalmocentra (Red Jurema )

1,6% DMT in the inner rootbark [2]


Mimosa scabrella
  • DMT in bark (Ott)


Mimosa verrucosa
  • DMT (Schultes 1969)


Mucuna pruriens
  • Leaves, seeds, stems and roots contain L-Dopa, Serotonin, 5-HTP, and Nicotine, as well as N,N-DMT, Bufotenine, and 5-MeO-DMT (Erowid)


Petalostylis labicheoides
var. casseoides
  • DMT in leaves and stems (Ott)


Diplopterys cabrerana (Chaliponga )
  • 1.3% DMT (Shulgin, TIHKAL)
  • Contains DMT (Ott)
  • Contains 5-MEO-DMT (Web Gossip)


Horsfieldia superba
  • 5-MeO-DMT and beta-carbolines (Jossang et al. 1991)


Iryanthera ulei
  • 5-MEO-DMT in bark (Ott)


Osteophloem platyspermum
  • DMT, 5-MEO-DMT in bark (Ott)


Virola

 Virola calophylla
  • Leaves 0.149% DMT (Ott)


Virola carinata
  • DMT in leaves (Ott)


Virola divergens
  • DMT in leaves (Ott)


Virola elongata
  • DMT, 5-MEO-DMT in bark and leaves (Ott)


Virola melinonii
  • DMT in bark (Ott)


Virola multinervia
  • DMT, 5-MEO-DMT in bark and leaves (Ott)


Virola pavonis
  • DMT in leaves (Ott)


Virola peruviana
  • DMT, 5-MEO-DMT in bark (Ott)


Virola rufuta
  • Alkaloids in bark and root, 95% of which is 5-MeO-DMT (Shulgin, TIHKAL)


Virola sebifera
  • DMT in bark (Ott)


Virola theiodora
  • DMT, 5-MEO-DMT in bark, roots, leaves and flowers (Ott)


Virola venosa
  • DMT, 5-MEO-DMT in roots and leaves (Ott)


Psychotria carthaginensis
  • 0.2% average DMT in dried leaves (Ott)


Psychotria viridis (Chacruna )
  • Leaves contain DMT - 0.10% to 0.66% (McKenna)



Extraction Teks

A/B

STB

STB-A/B hybrid

Dry tek

Dosages and consumption methods

History of usage

Scientific publications

Links of interest

  1. ↑ Southon et al. 1994. Phytochemical Dictionary of the Leguminosae. CRC Press. p. 71.
  2. ↑ L. M. Batista; R. N. Almeida; E. V. L. da-Cunha; M. S. da-Silva; J. M. Barbosa-Filho. Isolation and Identification of Putative Hallucinogenic Constituents from the Roots of Mimosa ophthalmocentra. In: Pharmaceutical Biology, Volume 37, Issue 1 January 1999

Subcategories

This category has only the following subcategory.

D

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