|
gptkbp:instanceOf
|
gptkb:chemical_compound
tryptamine
|
|
gptkbp:boilingPoint
|
n/a (decomposes)
|
|
gptkbp:CASNumber
|
608-07-1
|
|
gptkbp:category
|
psychoactive compound
indolealkylamine
|
|
gptkbp:chemicalFormula
|
C11H14N2O
|
|
gptkbp:discoveredBy
|
1958
|
|
gptkbp:foundIn
|
animals
plants
|
|
gptkbp:hasInChIKey
|
InChI=1S/C11H14N2O/c1-14-10-3-2-8-7-13-11(8)6-9(10)4-5-12/h2-3,7,13H,4-6,12H2,1H3
|
|
gptkbp:hasSMILES
|
COc1ccc2[nH]cc(CCN)c2c1
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
5-methoxytryptamine
|
|
gptkbp:IUPACName
|
2-(5-methoxy-1H-indol-3-yl)ethanamine
|
|
gptkbp:legalStatus
|
uncontrolled (most countries)
|
|
gptkbp:meltingPoint
|
87–89 °C
|
|
gptkbp:metabolism
|
gptkb:monoamine_oxidase
|
|
gptkbp:molecularWeight
|
190.24 g/mol
|
|
gptkbp:otherName
|
5-MT
5-methoxy-tryptamine
mexamine
|
|
gptkbp:pharmacological_effect
|
antioxidant
neurotransmitter
serotonin receptor agonist
|
|
gptkbp:predecessor
|
gptkb:melatonin
5-methoxyindoleacetic acid
|
|
gptkbp:PubChem_CID
|
1106
|
|
gptkbp:relatedTo
|
gptkb:melatonin
serotonin
5-methoxy-N,N-dimethyltryptamine
|
|
gptkbp:routeOfAdministration
|
oral
intraperitoneal
|
|
gptkbp:bfsParent
|
gptkb:N-acetyl-5-methoxytryptamine
|
|
gptkbp:bfsLayer
|
7
|