List of psychoactive plants

A list of plants that are used as psychoactive drugs. Some of them have been used entheogenically for millennia. The plants are listed according to the substances they contain.

Salvia divinorum, a dissociative hallucinogenic sage

Cannabinoids

Cannabis plant

Cannabis (Marijuana) is a popular psychoactive plant that is often used medically and recreationally. The psychoactive substance in Cannabis, THC, is unique in that it contains no nitrogen and is not an indole, tryptamine, phenethylamine, anticholinergic (deliriant), or a dissociative drug. Cannabis plants tend to vary, with different strains producing dynamic balances of cannabinoids (THC, CBD, etc.) yielding markedly different effects. Popular strains are often hybrids of Cannabis sativa and Cannabis indica.

Some universities and research firms currently study the medicinal effects of cannabis. Many jurisdictions have laws regulating or prohibiting the sale and use of medical and recreational cannabis.

Tryptamines

DMT Molecule in 2D
DMT Molecule in 3D

Many of the psychedelic plants contain dimethyltryptamine (DMT), which is either snorted (Virola, Yopo snuffs), vaporized, or drank with MAOIs (Ayahuasca). It cannot simply be eaten as it is not orally active without an MAOI and it needs to be extremely concentrated to be vaporized.

Acanthaceae

Species, Alkaloid content, where given, refers to dried material

Aceraceae

  • Acer saccharinum (Silver Maple Tree) was found to contain the indole alkaloid gramine (not active and extremely toxic) 0.05% in the leaves, so it is possible that other members of this plant family contain active compounds.[1]

Aizoaceae

  • Delosperma acuminatum, DMT, 5-MEO-DMT[2]
  • Delosperma cooperi, DMT, 5-MEO-DMT[2]
  • Delosperma ecklonis, DMT[2]
  • Delosperma esterhuyseniae, DMT[2]
  • Delosperma hallii, 5-MEO-DMT[2]
  • Delosperma harazianum, DMT, 5-MEO-DMT[2]
    Delosperma harazianum
    Shibam, DMT[2]
  • Delosperma hirtum, DMT[2]
    Delosperma hallii
    aff. litorale
  • Delosperma lydenbergense, DMT, 5-MEO-DMT[2]
  • Delosperma nubigenum, 5-MEO-DMT[2]
  • Delosperma pageanum, DMT, 5-MEO-DMT[2]
  • Delosperma pergamentaceum, Traces of DMT[2]
  • Delosperma tradescantioides, DMT[2]

Apocynaceae

Fabaceae (Leguminosae)

1,2,3,4-Tetrahydro-6-methoxy-2,9-dimethyl-beta-carboline, Plant,[45] 1,2,3,4-Tetrahydro-6-methoxy-2-methyl-beta-carboline, Plant,[42] 5-Methoxy-N,N-dimethyltryptamine, Bark,[42] 5-Methoxy-N-methyltryptamine, Bark,[42] Bufotenin, plant,[42] beans,[41] Bufotenin N-oxide, Fruit,[42] beans,[41] N,N-Dimethyltryptamine-oxide, Fruit[42][46]

Subfamily Caesalpinioideae

Lauraceae

    • Nectandra megapotamica, NMT[62]

Malpighiaceae

Myristicaceae

Ochnaceae

Pandanaceae

Poaceae (Gramineae)

Some Graminae (grass) species contain gramine, which can cause brain damage, other organ damage, central nervous system damage and death in sheep.[67]

None of the above alkaloids are said to have been found in Phalaris californica, Phalaris canariensis, Phalaris minor and hybrids of P. arundinacea together with P. aquatica.[69]

Polygonaceae

Punicaceae

  • Punica granatum "DMT in root cortex;"[61] The dried stem and root bark of the tree contain about 0.4-0.9% alkaloids.[71]

Rubiaceae

Rutaceae[74][75]

  • Dictyoloma incanescens, 5-MeO-DMT in leaves,[65] 0.04% 5-MeO-DMT in bark[53]
  • Dutaillyea drupacea, > 0.4% 5-MeO-DMT in leaves[30]
  • Dutaillyea oreophila, 5-MeO-DMT in leaves
  • Tetradium ruticarpum(syn. Evodia rutaecarpa), 5-MeO-DMT in leaves, fruit and roots
  • Limonia acidissima, 5-MeO-DMT in stems
  • Euodia leptococca (formerly Melicope), 0.2% total alkaloids, 0.07% 5-MeO-DMT; 5-MeO-DMT in leaves and stems, also "5-MeO-DMT-Oxide and a beta-carboline"[60]
  • Pilocarpus organensis, 5-MeO-DMT in leaves
  • Vepris ampody, Up to 0.2% DMT in leaves and branches[53]
  • Zanthoxylum arborescens, DMT in leaves
  • Zanthoxylum procerum, DMT in leaves
  • Citrus_limon, DMT, N-Methylated tryptamine derivative in leaves [76][77]
  • Citrus sinesis,DMT, N-Methylated tryptamine derivative [76][77]
  • Citrus bergamia,DMT, N-Methylated tryptamine derivative [76][77]
  • Mandarin_orange Traces of N-methylated tryptamine derivative in leaf. [78][77]
  • Chinotto Tree, N-Methylated tryptamine derivative in leaf [78][77]
  • Citrus medica, N-Methylated tryptamine derivative in leaf [78][77]

Phenethylamines

Species, Alkaloid Content (Fresh) - Alkaloid Content (Dried)

  • Coryphantha contains various PhEAs alkaloids including Macromerine Coryphanthine MethOxy-Candicine Corypalmine NMetCorypalmine and like compounds.[79][80]
Macromerine meta(ortho(CH3O)2)C6H3-CH(OH)-CH2N(CH3)2 , m(o(CH3O)2)C6H3-CH[O(-)]-CH2N(+)(CH3)3
p(-)O-C6H5-CH(H,OH,OCH3)CH2N(+)(CH3)3 and C6H5-CH[O(-)]-CH2N(+)(CH3)3
Coryphanthine C6H5-CH(OCH3)-CH2N(+)(CH3)3 , MeO-Candicine paraCH3O-C6H4-CH2CH2-N(+)(CH3)3

Beta-carbolines

Harmaline, a Beta-carboline

Beta-carbolines are "reversible" MAO-A inhibitors. They are found in some plants used to make Ayahuasca. In high doses the harmala alkaloids are somewhat hallucinogenic on their own. β-carboline is a benzodiazepine receptor inverse agonist and can therefore have convulsive, anxiogenic and memory enhancing effects.[92]

Apocynaceae

Bignoniaceae

Calycanthaceae

Chenopodiaceae

Combretaceae

Cyperaceae

Elaeagnaceae

Gramineae

Lauraceae

  • Nectandra megapotamica, Beta-carbolines[93]

Leguminosae

Loganiaceae

Malpighiaceae

Myristicaceae

Ochnaceae

Palmae

  • Plectocomiopsis geminiflora, Beta-carbolines[93]

Papaveraceae

Passifloraceae

Polygonaceae

  • Calligonum minimum, Beta-carbolines[93]
  • Leptactinia densiflora, Leptaflorine, etc.
  • Ophiorrhiza japonica, Harman
  • Pauridiantha callicarpoides, Harman
  • Pauridiantha dewevrei, Harman
  • Pauridiantha lyalli, Harman
  • Pauridiantha viridiflora, Harman
  • Simira klugei, Harman
  • Simira rubra, Harman

Rubiaceae

Rutaceae

Sapotaceae

Simaroubaceae

Solanaceae

Symplocaceae

Tiliaceae

  • Grewia mollis, Beta-carbolines[93]

Zygophyllaceae

Plants containing other psychoactive substances

Substance Plant Comment
Asarone Acorus calamus Asarone
Yohimbine Alchornea floribunda Yohimbine
Arecoline Areca catechu Areca nut or betel
Unknown

Argemone mexicana

Used by Chinese residents of Mexico during the early 20th century as a legal substitute for opium and currently smoked as a marijuana substitute.

Ergine

Argyreia nervosa (Hawaiian Baby Woodrose)

Seeds contain high amounts of ergine (also known as LSA, lysergamide, or lysergic acid amide), often 50-150X the amounts found in Ipomoea violacea.
Thujone Artemisia absinthium Additive to absinthe. Also called "wormwood"
Unknown Asiminia TrilobaL. Identical alkaloid to morphine[102]
Tropane alkaloids Atropa belladonna Deadly nightshade
Tropane alkaloids Brugmansia Angel's trumpets
Unknown

Calea zacatechichi

Produces vivid dreams after smoking. It is also employed by the Chontal people as a medicinal herb against gastrointestinal disorders, and is used as an appetizer, cathartic anti-dysentery remedy, and as a fever-reducing agent. Its psychedelic properties do not become apparent until the user is asleep. Reports describe rituals that involve drinking it as a tea to induce divinatory or lucid dreams due to its properties as an oneirogen.[103]
Caffeine Camellia sinensis Tea leaves, tea, native to Asia

Cathinone

Catha edulis

Khat[104]
Vincristine Catharanthus roseus Catharanthus roseus is (perhaps unpleasantly) "hallucinogenic."[105]
Unknown Cestrum nocturnum Night-blooming jasmine
Caffeine Coffea arabica Coffee beans, coffee, native to Africa
Caffeine Cola Cola or kola nut, traditional additive to cola, native to Africa
Unknown

Coleus

Unknown

Bulbocapnine

Corydalis solida, cava

Bulbocapnine, Nantenine, Tetrahydropalmatine
Tropane alkaloids Datura Thorn apple, devil's trumpets, loco weed, Jimson weed
Cytisine Dermatophyllum Mescal bean
Unknown Desfontainia spinosa Causes visions[106]
Nicotine Duboisia hopwoodii Pituri
Unknown Entada rheedii African dream herb
Ephedrine Ephedra sinica Ephedra
Cocaine Erythroxylum coca Coca. Widely used illegal stimulant, produces hallucination in overdose, native to South America
Unknown Fittonia albivenis Nerve or mosaic plant
Unknown

Foeniculum vulgare

Unknown

Himbacine

Galbulimima belgraveana Galbulimima belgraveana is rich in alkaloids and twenty-eight alkaloids have been isolated including himbacine.

Glaucine

Glaucium flavum

Glaucine
Unknown Heimia myrtifolia Auditory
Unknown Heimia salicifolia Auditory[107]
Lobeline Hippobroma longiflora Star of Bethlehem
Hyperforin Hypericum perforatum Saint John's wort
Tropane alkaloids Hyoscyamus Henbane
Caffeine, Theobromine, Dimethylxanthines Ilex guayusa Ilex guayusa is used as an additive to some versions of Ayahuasca. According to the Ecuadorian indigenous, it is also slightly hallucinogenic on its own, when drunk in high enough quantities.
Ergine

Ipomoea tricolor & Ipomoea violacea

Ergine in seeds; up to 0.12% total[108]
Unknown Justicia pectoralis Unknown
Lactucarium

Lactuca virosa

Lactucarium

Lagochilin

Lagochilus inebrians Lagochilin is thought to be responsible for the sedative, hypotensive and hemostatic effects of this plant.

Pukateine

Laurelia novae-zelandiae

Pukateine
Unknown Rollinia mucosa Rollinia mucosa is said to be narcotic [102]

Leonurine

Leonotis leonurus

Both leaves and flowers (where most concentrated) contain Leonurine. (Effects reminiscent of marijuana)
Nicotine[109]
Leucas aspera
Nicotine

Leonurine

Leonotis nepetifolia

Both leaves and flowers (where most concentrated) contain Leonurine. (Effects reminiscent of marijuana)
Lobeline Lobelia inflata Indian tobacco
Unknown

Magnolia virginiana

[110]
Tropane alkaloids Mandragora officinarum Mandrake
Ergine Some Mirabilis spp. Possibly contains ergine
Mitragynine Mitragyna speciosa Kratom
Myristicin Myristica fragrans Nutmeg
Aporphine Nelumbo nucifera Sacred lotus
Nepetalactone Nepeta cataria Catnip
Nicotine Nicotiana tabacum Tobacco. Can cause hallucination in very large doses

Aporphine, Apomorphine

Nymphaea caerulea

Blue lotus or lily. Recent studies have shown Nymphaea caerulea to have psychedelic properties, and may have been used as a sacrament in ancient Egypt and certain ancient South American cultures. Dosages of 5 to 10 grams of the flowers induces slight stimulation, a shift in thought processes, enhanced visual perception, and mild closed-eye visuals. Nymphaea caerulea is related to, and possesses similar activity as Nelumbo nucifera, the Sacred Lotus. Both Nymphaea caerulea and Nelumbo nucifera contain the alkaloids nuciferine and apomorphine, which have been recently isolated by independent labs.

These psychoactive effects make Nymphaea caerulea a likely candidate (among several) for the lotus plant eaten by the mythical Lotophagi in Homer's Odyssey.

Used in aromatherapy, Nymphaea caerulea is purported to have a "divine" essence, bringing euphoria, heightened awareness and tranquility.

Other sources cite anti-spasmodic and sedative, purifying and calming properties.

Heliamine Pachycereus pringlei Largest cactus in the world. Heliamine bears some similarities to mescaline
Ginsenosides Panax Ginseng
Morphine Papaver somniferum Opium. Widely used analgesic, native to the Old World
Chrysin Passiflora Passion flower
Unknown Phytolacca americanaL. Naroctic and toxic when root is consumed.[102]
Yohimbine Pausinystalia johimbe Yohimbe
Unknown Pedicularis densiflora Indian warrior

Kavalactones

Piper methysticum

Kavalactones
Ergine Rivea corymbosa Seeds contain ergine, lysergol, and turbicoryn; lysergic acid alkaloids up to 0.03%[111]

Salvinorin A

Salvia divinorum

Salvinorin A, 0.89-3.87 mg/g, also Salvinorin B and Salvinorin C[112]
Mesembrine Sceletium tortuosum Kanna
Baicalein Scutellaria Skullcaps
Unknown

Silene capensis

Produces vivid dreams after smoking.
Unknown

Tagetes lucida

Anethole, Chavicol, Coumarin, Estragole, Isorhamnetin, Methyleugenol, Quercitin

Ibogaine

Tabernanthe iboga

Ibogaine in root bark[113]

Ibogaine

Tabernanthe orientalis

Ibogaine in root leaves[113]
Voacangine

Tabernaemontana divaricata

Voacangine is similar to ibogaine. It potentiated effect of barbituarates which may possibly mean voacangine is psychoactive.

Ibogaine

Tabernanthe pubescens

Ibogaine and similar alkaloids[113]

Ibogaine

Tabernaemontana sp.

Ibogaine[113]
Theobromine Theobroma cacao Cocoa or cacao bean, chocolate, native to the Americas

Ibogaine

Trachelospermum jasminoides

Ibogaine, coronaridine, voacangine, apparicine, conoflorine, and 19-epi-voacangarine[114][115]
Damianin

Turnera diffusa

Damianin
Actinidine Valeriana officinalis Valerian
Vincamine Vinca minor Vincamine
Voacangine Voacanga africana Voacangine is similar to ibogaine
Unknown Zornia latifolia Zornia latifolia is mentioned in Food of the Gods as "an hallucinogenic substitute for cannabis". It is nicknamed Maconha brava because locals use it as a cannabis substitute.

See also

References

  1. "IJ PACHTER, DE ZACHARIAS, O RIBEIRO - The Journal of Organic Chemistry, 1959 -" (PDF). Pubs.acs.org. Retrieved 22 December 2017.
  2. "Trout's Notes on Some Other Succulents". Archived from the original on 2015-09-24. Retrieved 2015-01-14.
  3. "Profiles of Psychedelic Drugs". paranoia.lycaeum.org. Archived from the original on 2002-05-22. Retrieved 2008-04-19.
  4. "Lycaeum > Leda > Acacia acuminata". leda.lycaeum.org. Archived from the original on 2007-10-12. Retrieved 2008-02-23.
  5. "Plants & Seeds > A > Acacia spp". Shaman Australis Botanicals. Retrieved 14 January 2015.
  6. Glasby, John Stephen (1991). Dictionary of Plants Containing Secondary Metabolites. CRC Press. p. 2. ISBN 978-0-85066-423-2.
  7. Nutritive value assessment of the tropical shrub legume Acacia angustissima: anti-nutritional compounds and in vitro digestibility. Personal Authors: McSweeney, C. S., Krause, D. O., Palmer, B., Gough, J., Conlan, L. L., Hegarty, M. P.Author Affiliation: CSIRO Livestock Industries, Long Pocket Laboratories, 120 Meiers Road, Indooroopilly, Qld 4068, Australia. Document Title: Animal Feed Science and Technology, 2005 (Vol. 121) (No. 1/2) 175-190
  8. "Maya Ethnobotanicals - Ayahuasca, Rainforest Plants, Folklore, Incenses, Art & Visions". Archived from the original on 25 October 2008. Retrieved 14 January 2015.
  9. Black Panther. "Akacje". Herbarium.0-700.pl. Retrieved 14 January 2015.
  10. "Lycaeum > Leda > Acacia auriculiformis". Leda.lycaeum.org. Archived from the original on 7 December 2008. Retrieved 14 January 2015.
  11. Hegnauer, R. (1996-07-30). Caesalpinioideae und Mimosoideae. ISBN 9783764351656. Retrieved 14 January 2015 via Books.google.com.
  12. Australian Bush Food and Native Medicine Forum members. "Australian Bushfood (Bushtucker) and Native Medicine Forum". Bushfood.net. Archived from the original on 4 August 2014. Retrieved 14 January 2015.
  13. "Entheology.org - Preserving Ancient Knowledge". Entheology.org. Retrieved 22 December 2017.
  14. "Ask Dr. Shulgin Online September 26, 2001". Cognitiveliberty.org. Retrieved 14 January 2015.
  15. Index of Rätsch, Christian. Enzyklopädie der psychoaktiven Pflanzen, Botanik, Ethnopharmakologie und Anwendungen, 7. Auflage. AT Verlag, 2004, 941 Seiten. ISBN 3-85502-570-3 at "Enzyklopädie der psychoaktiven Pflanzen". Archived from the original on 2007-10-10. Retrieved 2007-06-13. (in German)
  16. "Dr Karl's Q&A forum". Abc.net.au. Retrieved 14 January 2015.
  17. "comp phyto". Users.lycaeum.org. Archived from the original on 7 December 2008. Retrieved 14 January 2015.
  18. "acacias and entheogens". Users.lycaeum.org. Archived from the original on 7 December 2008. Retrieved 14 January 2015.
  19. "Lycaeum > Leda > Acacia complanata". Users.lycaeum.org. Archived from the original on 7 December 2008. Retrieved 14 January 2015.
  20. NMR spectral assignments of a new chlorotryptamine alkaloid and its analogues from Acacia confusa Malcolm S. Buchanan, Anthony R. Carroll, David Pass, Ronald J. Quinn Magnetic Resonance in Chemistry Volume 45, Issue 4, pp. 359–361. John Wiley & Sons, Ltd.
  21. "Naturheilpraxis - Fachforum - Die Heilkraft der Akazien – Ein einführender Überblick". 5 January 2010. Archived from the original on 5 January 2010. Retrieved 22 December 2017.
  22. "Lycaeum > Leda > Acacia cultriformis". Leda.lycaeum.org. Archived from the original on 7 December 2008. Retrieved 14 January 2015.
  23. "Plant Choices - Phytochemeco Databases". Ars-grin.gov. Archived from the original on 27 December 2014. Retrieved 14 January 2015.
  24. Vivid Interactive and Design. "Rural Industries Research and Development Corporation - Page Not Found" (PDF). Archived from the original (PDF) on 17 December 2008. Retrieved 14 January 2015. Cite uses generic title (help)
  25. "www.bpi.da.gov.ph" (PDF). Archived from the original (PDF) on July 20, 2011.
  26. "Acacia farnesiana". Hort.purdue.edu. Retrieved 14 January 2015.
  27. Hegnauer, Robert (1994). Chemotaxonomie der Pflanzen. Springer. p. 500. ISBN 978-3-7643-2979-2.
  28. "Lycaeum > Leda > Acacia floribunda". leda.lycaeum.org. Archived from the original on 2007-10-12. Retrieved 2008-02-23.
  29. Voogelbreinder, S. "Garden Of Eden" 2009
  30. "Lista över hallucinogena växter, svampar och djur". Wiki.magiskamolekyler.org. Retrieved 14 January 2015.
  31. "Lycaeum > Leda > Acacia longifolia". leda.lycaeum.org. Archived from the original on 2007-06-27. Retrieved 2008-02-23.
  32. extentech.sheetster.com
  33. S. Voogelbreinder "Garden Of Eden" 2009
  34. "Lista över hallucinogena växter, svampar och djur - Magiska Molekylers Wiki". wiki.magiskamolekyler.org.
  35. "obtusifolia phyto". Users.lycaeum.org. Archived from the original on 3 December 2008. Retrieved 14 January 2015.
  36. Plants Containing DMT (German) Archived 2007-06-29 at the Wayback Machine
  37. "Acacia campylacantha - Hortipedia". www.hortipedia.org. Archived from the original on 2007-10-12. Retrieved 2008-02-23.
  38. "Acacia rigidula - Magiska Molekylers Wiki". wiki.magiskamolekyler.org. Retrieved 2008-02-23.
  39. "Chemistry of Acacias from South Texas" (PDF). Archived from the original (PDF) on May 15, 2011.
  40. "Eins". Factorey.ch. Archived from the original on 12 August 2008. Retrieved 22 December 2017.
  41. Granier-Doyeux, Marcel (January 1, 1965). "Native hallucinogenic drugs piptadenias". United Nations Office on Drugs and Crime. Archived from the original on January 20, 2005. Retrieved February 28, 2019.
  42. Dr. Duke's Archived 2004-11-10 at the Wayback Machine Phytochemical and Ethnobotanical Databases
  43. "Cultivo de Curupay, Cebil colorado (Anadenanthera colubrina) y usos, herbotecnia". Herbotecnia.com.ar. Retrieved 14 January 2015.
  44. "Bufo alvarius - Jonathan Ott on Bufotenine". Erowid.org. Retrieved 2008-02-23.
  45. Dr. Duke's Archived 2013-02-19 at the Wayback Machine Phytochemical and Ethnobotanical Databases
  46. Stafford, Peter (2013-02-18). Psychedelics Encyclopedia. ISBN 9781579511692. Retrieved 14 January 2015 via Books.google.com.
  47. Ott, J. (July–September 2001). "Pharmañopo-psychonautics: human intranasal, sublingual, intrarectal, pulmonary and oral pharmacology of bufotenine". Journal of Psychoactive Drugs. 33 (3): 273–81. doi:10.1080/02791072.2001.10400574. PMID 11718320. S2CID 5877023.
  48. "Erowid Online Books : "Ayahuasca: alkaloids, plants, and analogs" by Keeper of the Trout". Erowid.org. Retrieved 14 January 2015.
  49. Hegnauer, R. (1996-07-30). Google Book Search. ISBN 978-3-7643-5165-6. Retrieved 2008-05-08.
  50. "Desmodium caudatum". Germplasm Resources Information Network (GRIN). Agricultural Research Service (ARS), United States Department of Agriculture (USDA). Retrieved 2008-05-02.
  51. "Pharmaceutical, Nutraceutical and Industrial Potential of Temperate Legumes" (PDF). Archived from the original (PDF) on 2014-04-17. Retrieved 2015-01-14.
  52. "Trout's Notes on Desmodium" (PDF). Archived from the original (PDF) on August 31, 2005.
  53. "Erowid Psychoactive Vaults : Tryptamine FAQ". Erowid.org. Retrieved 14 January 2015.
  54. "Isolation and Identification of Putative Hallucinogenic Constituents from the Roots of Mimosa ophthalmocentra". Pharmaceutical Biology.
  55. Hegnauer, R. (1996-07-30). Google Book Search. ISBN 978-3-7643-5165-6. Retrieved 2008-05-07.
  56. "Ask Erowid : ID 75 : What is the DMT content of Mimosa hostilis rootbark?". Erowid.org. Retrieved 14 January 2015.
  57. "UNODC Bulletin on Narcotics 1969". Archived from the original on 2007-07-08.
  58. "Erowid Mucuna pruriens Vault". Erowid.org. Retrieved 14 January 2015.
  59. "Kalifornischer Korallenstrauch (Erythrina decora) im GIFTPFLANZEN.COMpendium - giftpflanzen.com". Giftpflanzen.com. Retrieved 2008-04-18.
  60. "tryptamines: fungi". Bluezoo.org. Retrieved 14 January 2015.
  61. "Plants Containing DMT List". Dmt-nexus.com. Retrieved 22 December 2017.
  62. Ott, Jonathan (1996). Pharmacotheon. p. 219.
  63. "Species Information". sun.ars-grin.gov. Archived from the original on 2004-11-10. Retrieved 2008-04-11.
  64. "5-MEO-DMT". Tryptamines.com. Retrieved 14 January 2015.
  65. "Committee for veterinary medicinal products virola sebifera summary report" (PDF). Archived from the original (PDF) on July 10, 2007.
  66. Peter R. Cheeke (1989). Toxicants of Plant Origin. CRC-Press. p. 169. ISBN 978-0-8493-6990-2. Retrieved 2008-04-20 via books.google.com.
  67. "Erowid Arundo donax Vaults : Trout's Notes on Tryptamine Content of Arundo donax". Erowid.org. Retrieved 14 January 2015.
  68. "DMT, Life and the Universe". Nepenthes.lycaeum.org. Archived from the original on 2008-06-18. Retrieved 14 January 2015.
  69. "Erowid Phalaris Vault : FAQ 2.01". Erowid.org. Retrieved 14 January 2015.
  70. "Herb Datanz". Herb Datanz. Archived from the original on 12 May 2017. Retrieved 22 December 2017.
  71. "Psychotria poeppigiana - Uragoga tomentosa". Discover Life. Retrieved 2013-10-14.
  72. "Amazing Nature". Amazing-nature.com. Archived from the original on 27 September 2007. Retrieved 22 December 2017.
  73. Servillo, L; Giovane, A; Balestrieri, ML; Cautela, D; Castaldo, D (Sep 2012). "N-methylated tryptamine derivatives in citrus genus plants: identification of N,N,N-trimethyltryptamine in bergamot". Journal of Agricultural and Food Chemistry. 60 (37): 9512–8. doi:10.1021/jf302767e. PMID 22957740.
  74. Servillo, L; Giovane, A; Balestrieri, ML; Casale, R; Cautela, D; Castaldo, D (May 2013). "Citrus genus plants contain N-methylated tryptamine derivatives and their 5-hydroxylated forms". Journal of Agricultural and Food Chemistry. 61 (21): 5156–62. doi:10.1021/jf401448q. PMID 23682903.
  75. "Citrus Growers Manufacture Huge Amounts of DMT".
  76. "Citrus Genus Plants Contain N-Methylated Tryptamine Derivatives and Their 5-Hydroxylated Forms".
  77. "CitrusGenus Plants Contain N‑Methylated Tryptamine Derivativesand Their 5‑Hydroxylated Forms" (PDF).
  78. Meyer, B. N.; Helfrich, J. S.; Nichols, D. E.; McLaughlin, J. L.; Davis, D. V.; Cooks, R. G. (1983). "Cactus Alkaloids. LIII. Coryphanthine and O-Methyl-Candicine, Two New Quaternary Alkaloids from Coryphantha greenwoodii". Journal of Natural Products. 46 (5): 688–693. doi:10.1021/np50029a017.
  79. N. Meyer, B; S. Helfrich, J; Nichols, David; L. McLaughlin, J; V. Davis, D; G. Cooks, R (1 July 2004). "Cactus Alkaloids. LIII. Coryphanthine and O-Methyl-Candicine, Two New Quaternary Alkaloids from Coryphantha greenwoodii". Journal of Natural Products. 46 (5): 688–693. doi:10.1021/np50029a017. Retrieved 22 December 2017 via ResearchGate.
  80. "Partial List of Alkaloids in Trichocereus Cacti". Thenook.org. Retrieved 2013-10-14.
  81. a1b2c3.com. "Trichocereus spp. Information". A1b2c3.com. Retrieved 22 December 2017.
  82. "Erowid Cacti Vaults : Visionary Cactus Guide - Mescaline from Sawdust". Erowid.org. Retrieved 14 January 2015.
  83. Forbidden Fruit Archives Archived 2005-11-28 at the Wayback Machine
  84. "Descriptions of psychoactive Cacti". Users.lycaeum.org. Archived from the original on 15 July 2009. Retrieved 14 January 2015.
  85. "Austrocylindropuntia cylindrica". Desert-tropicals.com. Retrieved 22 December 2017.
  86. "Cane Cholla (Cylindropuntia spinosior )". Desert-tropicals.com. Retrieved 14 January 2015.
  87. "Partial List of Alkaloids in Trichocereus Cacti". Thennok.org. Retrieved 22 December 2017.
  88. "Echinopsis tacaquirensis ssp. taquimbalensis". Desert-tropicals.com. Retrieved 14 January 2015.
  89. "Cardon Grande (Echinopsis terscheckii)". Desert-tropicals.com. Retrieved 14 January 2015.
  90. Venault P, Chapouthier G (2007). "From the behavioral pharmacology of beta-carbolines to seizures, anxiety, and memory". ScientificWorldJournal. 7: 204–23. doi:10.1100/tsw.2007.48. PMC 5901106. PMID 17334612.
  91. "Cornell University Department of Animal Science". Ansci.cornell.edu. Retrieved 14 January 2015.
  92. Callaway, JC; Brito, GS; Neves, ES (2005). "Phytochemical analyses of Banisteriopsis caapi and Psychotria viridis". Journal of Psychoactive Drugs. 37 (2): 145–150. doi:10.1080/02791072.2005.10399795. PMID 16149327. S2CID 30736017.
  93. Glasby, J. S. (2002-09-11). Directory Of Plants Containing Secondary Metabolites. ISBN 9780203489871. Retrieved 14 January 2015 via Books.google.com.
  94. "Chemical Information". sun.ars-grin.gov. Archived from the original on 2004-11-21. Retrieved 2008-04-11.
  95. "Silbrige Ayahuasca-Liane (Banisteriopsis muricata) im GIFTPFLANZEN.COMpendium". Giftpflanzen.com. Retrieved 2008-04-18.
  96. "Erowid Online Books : "Ayahuasca: alkaloids, plants, and analogs" by Keeper of the Trout". Erowid.org. Retrieved 22 December 2017.
  97. "Passion Flower". Drugs.com. Retrieved 14 January 2015.
  98. "www.amazing-nature.com". Archived from the original on September 27, 2007.
  99. Ma, ZZ; Hano, Y; Nomura, T; Chen, YJ (April 2000). "Alkaloids and phenylpropanoids from Peganum nigellastrum". Phytochemistry. 53 (8): 1075–8. doi:10.1016/S0031-9422(99)00440-9. PMID 10820833. Retrieved 2008-01-12.
  100. Denise Otsuka, Rafaela; Otsuka, Rafaela Denise; Lago, Joao Henrique Ghilardi; Rossi, Lucia; Galduroz, Jose Carlos Fernandes; Rodrigues, Eliana (2010). "Psychoactive Plants Described in a Brazilian Literary Work and their Chemical Compounds". Central Nervous System Agents in Medicinal Chemistry. 10 (3): 218–237. doi:10.2174/1871524911006030218. PMID 20557283 via www.academia.edu.
  101. Sałaga, Maciej; Fichna, Jakub; Socała, Katarzyna; Nieoczym, Dorota; Pieróg, Mateusz; Zielińska, Marta; Kowalczuk, Anna; Wlaź, Piotr (2016). "Neuropharmacological characterization of the oneirogenic Mexican plant Calea zacatechichi aqueous extract in mice". Metabolic Brain Disease. 31: 631–641. doi:10.1007/s11011-016-9794-1. ISSN 0885-7490. PMC 4863909. PMID 26821073.
  102. Al Zarouni, Yousif (2015). The Effects of Khat (Catha Edulis) (First ed.). London: Yousif Al Zarouni. p. 5. ISBN 978-1-326-24867-3.
  103. "Protected Blog". Sliceoftheday. Retrieved 14 January 2015.
  104. Schultes, Richard Evans, Iconography of New World Plant Hallucinogens. p. 101
  105. "Erowid Sinicuichi Vault : FAQ (heimia salicifolia Frequently Asked Questions)". Erowid.org. Retrieved 14 January 2015.
  106. "Trichterwinde (Ipomoea violacea) im GIFTPFLANZEN.COMpendium". Giftpflanzen.com. Retrieved 2008-04-18.
  107. Mangathayaru, K; Thirumurugan, D; Patel, PS; Pratap, DV.V; David, DJ; Karthikeyan, J (2006). "Isolation and identification of nicotine from leucas aspera (willd) link". Indian Journal of Pharmaceutical Sciences. 68 (1): 88. doi:10.4103/0250-474X.22972. ISSN 0250-474X.
  108. Rätsch, Christian (25 April 2005). The Encyclopedia of Psychoactive Plants: Ethnopharmacology and Its Applications. Inner Traditions/Bear. ISBN 9781594776625. Retrieved 22 December 2017 via Google Books.
  109. "Ololiuqui (Rivea corymbosa) im GIFTPFLANZEN.COMpendium". Giftpflanzen.com. Retrieved 2008-04-18.
  110. "Salvia divinorum Clones". Sagewisdom.org. Retrieved 14 January 2015.
  111. "Erowid Online Books : "TIHKAL" - #25 IBOGAINE". Erowid.org. Retrieved 14 January 2015.
  112. Dr. B. Bös. "Sternjasmin (Trachelospermum jasminoides) im GIFTPFLANZEN.COMpendium - giftpflanzen.com". Giftpflanzen.com. Retrieved 14 January 2015.
  113. "Indole Alkaloids from Trachelospermum jasminoides".

Bibliography

  • Al Zarouni, Yousif (2015). The Effects of Khat (Catha Edulis). London: Yousif Al Zarouni.
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