DMT (N,N-Dimethyltryptamine)

URI: https://gptkb.org/entity/DMT_(N,N-Dimethyltryptamine)

GPTKB entity

Statements (52)

Predicate	Object
gptkbp:instanceOf	alkaloid Hallucinogen
gptkbp:aroma	indolic
gptkbp:ATCCode	none
gptkbp:biosynthesized_from	tryptophan
gptkbp:boilingPoint	160 °C (at 0.5 mmHg)
gptkbp:CASNumber	61-50-7
gptkbp:category	alkaloid Hallucinogen serotonergic psychedelic
gptkbp:chemicalFormula	C12H16N2
gptkbp:color_(pure)	white
gptkbp:discoveredBy	gptkb:Richard_Helmuth_Fredrick_Manske
gptkbp:discoveredIn	1931
gptkbp:effect	mystical experiences hallucinations altered perception of time
gptkbp:featured_in_book	gptkb:DMT:_The_Spirit_Molecule
gptkbp:firstSynthesized	1931
gptkbp:foundIn	some animals various plants
gptkbp:halfLife	~15 minutes (inhaled)
gptkbp:hasStreet	gptkb:Dimitri the spirit molecule
https://www.w3.org/2000/01/rdf-schema#label	DMT (N,N-Dimethyltryptamine)
gptkbp:IUPACName	N,N-Dimethyl-1H-indole-3-ethanamine
gptkbp:legalStatus	gptkb:Schedule_I_(US) gptkb:Class_A_(UK)
gptkbp:meltingPoint	44–46 °C
gptkbp:metabolism	gptkb:monoamine_oxidase
gptkbp:molecularWeight	188.27 g/mol
gptkbp:notableContributor	gptkb:Rick_Strassman
gptkbp:PubChem_CID	gptkb:CHEMBL39122 6089 5867
gptkbp:relatedTo	gptkb:5-MeO-DMT gptkb:bufotenin
gptkbp:risk_of_dependence	low
gptkbp:routeOfAdministration	injection inhalation oral (with MAOI)
gptkbp:solubility	slightly soluble in water soluble in ethanol soluble in chloroform
gptkbp:target	gptkb:sigma-1_receptor 5-HT2A receptor
gptkbp:toxicity	low (in typical doses)
gptkbp:traditionalUse	South American shamanism
gptkbp:UNII	WUB6018FEM
gptkbp:used_in	gptkb:ayahuasca
gptkbp:bfsParent	gptkb:DMT:_The_Spirit_Molecule
gptkbp:bfsLayer	7