Bufotenin

Bufotenin
Clinical data
Other namesBufotenine; 5-Hydroxy-N,N-dimethyltryptamine; 5-HO-DMT; 5-OH-DMT; N,N-Dimethyl-5-hydroxytryptamine; N,N-Dimethylserotonin; Dimethylserotonin; Dimethyl-5-HT; Cebilcin; Mappine
Routes of
administration
Oral, intranasal/insufflation, inhalation, sublingual, rectal, intravenous
Drug classSerotonergic psychedelic; Hallucinogen; Serotonin receptor agonist; Serotonin 5-HT2A receptor agonist
ATC code
  • None
Legal status
Legal status
Pharmacokinetic data
BioavailabilityWeakly active (with or without MAOITooltip monoamine oxidase inhibitor)
MetabolismDeamination via MAO-ATooltip monoamine oxidase A and conjugation (glucuronidation, sulfation)
Metabolites5-HIAATooltip 5-Hydroxyindoleacetic acid
Glucuronide and sulfate conjugates
Onset of actionPOTooltip Oral administration: 20 min
INTooltip Intranasal administration: 5–15 min
SLTooltip Sublingual administration: 5–15 min
RECTooltip Rectal administration: ~15 min
INHTooltip Inhalational administration: ≤1–2 min
IVTooltip Intravenous injection: <1 min
Duration of actionPOTooltip Oral administration: ~2 hours
INTooltip Intranasal administration: 30–90 min
SLTooltip Sublingual administration: 30–90 min
RECTooltip Rectal administration: ~1 hour
INHTooltip Inhalational administration: 60–90 min
IVTooltip Intravenous injection: ~5–120 min
Identifiers
  • 3-[2-(Dimethylamino)ethyl]-1H-indol-5-ol
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.006.971
Chemical and physical data
FormulaC12H16N2O
Molar mass204.273 g·mol−1
3D model (JSmol)
Melting point146 to 147 °C (295 to 297 °F)
Boiling point320 °C (608 °F)
  • CN(C)CCc1c[nH]c2ccc(O)cc12
  • InChI=1S/C12H16N2O/c1-14(2)6-5-9-8-13-12-4-3-10(15)7-11(9)12/h3-4,7-8,13,15H,5-6H2,1-2H3 Y
  • Key:VTTONGPRPXSUTJ-UHFFFAOYSA-N Y
  (verify)

Bufotenin, also known as dimethylserotonin or as 5-hydroxy-N,N-dimethyltryptamine (5-HO-DMT), is a serotonergic psychedelic of the tryptamine family. It is a derivative of the psychedelic dimethyltryptamine (DMT) and of the neurotransmitter serotonin (5-hydroxytryptamine; 5-HT). The compound is an alkaloid found in some species of mushrooms, plants, and toads. It is also found naturally in the human body in small amounts. Bufotenin, for instance derived from the trees Anadenanthera colubrina and Anadenanthera peregrina, has a long history of entheogenic use as a snuff in South America.

The name bufotenin originates from the toad genus Bufo, which includes several species of psychoactive toads, most notably Incilius alvarius (formerly Bufo alvarius), that secrete bufotoxins from their parotoid glands. However, Bufo and related species like Incilius alvarius contain only trace amounts of bufotenin, with their major active component instead being 5-MeO-DMT. In addition to DMT and serotonin, bufotenin is similar in chemical structure to other psychedelics such as 5-MeO-DMT and psilocin (4-HO-DMT). These compounds also occur in some of the same fungus, plant, and animal species as bufotenin.

Bufotenin acts as a potent and non-selective serotonin receptor agonist, including of the serotonin 5-HT1A, 5-HT2A, 5-HT2C, and 5-HT3 receptors, among others. It also acts as a potent and specific serotonin releasing agent. The compound is more hydrophilic than other related tryptamines and consequently is more peripherally selective. In relation to this, bufotenin has been associated with prominent peripheral serotonergic side effects, such as cardiovascular changes. The cardiovascular effects of bufotenin can be powerful and potentially dangerous.

For many decades and even into the present, bufotenin has been considered by many experts, such as David E. Nichols, to be either inactive or only weakly active as a psychedelic in humans and to produce robust toxic effects. Alexander Shulgin was also uncertain whether bufotenin was an active psychedelic. However, Jonathan Ott found in 2001 via self-experimentation that bufotenin is in fact a potent psychedelic and does not necessarily produce serious adverse effects. Hamilton Morris has further supported these findings with his own self-experimentation, although bufotenin was reported to be strongly nauseating for himself and many others. According to Morris, the psychedelic effects of bufotenin are like a cross between those of DMT and 5-MeO-DMT. Morris has stated that bufotenin may in fact be the psychedelic with the longest history of human entheogenic use. Bufotenin has also been encountered as a recreational drug in forensic samples, for instance in New York City.