This HTML5 document contains 48 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n2http://linked.opendata.cz/resource/drugbank/drug/
dctermshttp://purl.org/dc/terms/
n6http://linked.opendata.cz/resource/drugbank/drug/DB01488/identifier/chemspider/
n11http://linked.opendata.cz/resource/drugbank/drug/DB01488/identifier/wikipedia/
n17http://bio2rdf.org/drugbank:
n9http://linked.opendata.cz/resource/drugbank/drug/DB01488/identifier/kegg-compound/
n10http://linked.opendata.cz/resource/drugbank/drug/DB01488/identifier/pubchem-compound/
admshttp://www.w3.org/ns/adms#
n16http://wifo5-03.informatik.uni-mannheim.de/drugbank/resource/drugs/
n8http://linked.opendata.cz/resource/drugbank/drug/DB01488/identifier/pubchem-substance/
n7http://linked.opendata.cz/resource/drugbank/drug/DB01488/identifier/drugbank/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n13http://linked.opendata.cz/resource/drugbank/drug/DB01488/identifier/iuphar/
owlhttp://www.w3.org/2002/07/owl#
n3http://linked.opendata.cz/ontology/drugbank/
n12http://linked.opendata.cz/resource/drugbank/drug/DB01488/identifier/guide-to-pharmacology/
n4http://linked.opendata.cz/resource/drugbank/property/
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DB01488
rdf:type
n3:Drug
n3:description
An N-methylated indoleamine derivative, a serotonergic hallucinogen found in several plants, especially Prestonia amazonica (Apocynaceae) and in mammalian brain, blood, and urine. It apparently acts as an agonist at some types of serotonin receptors and an antagonist at others. [PubChem]
n3:generalReferences
# Strassman RJ, Qualls CR: Dose-response study of N,N-dimethyltryptamine in humans. I. Neuroendocrine, autonomic, and cardiovascular effects. Arch Gen Psychiatry. 1994 Feb;51(2):85-97. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/8297216 # Callaway JC: A proposed mechanism for the visions of dream sleep. Med Hypotheses. 1988 Jun;26(2):119-24. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/3412201
n3:group
illicit experimental
n3:indication
Some people use this compound as a psychedelic inducing agent.
owl:sameAs
n16:DB01488 n17:DB01488
dcterms:title
Dimethyltryptamine
adms:identifier
n6:5864 n7:DB01488 n8:46507463 n9:C08302 n10:6089 n11:Dimethyltryptamine n12:141 n13:141
n3:mechanismOfAction
DMT acts as a non-selective agonist at most or all of the serotonin receptors.
n3:IUPAC-Name
n4:271B4F40-363D-11E5-9242-09173F13E4C5
n3:InChI
n4:271B4F46-363D-11E5-9242-09173F13E4C5
n3:Molecular-Formula
n4:271B4F45-363D-11E5-9242-09173F13E4C5
n3:Molecular-Weight
n4:271B4F42-363D-11E5-9242-09173F13E4C5
n3:Monoisotopic-Weight
n4:271B4F43-363D-11E5-9242-09173F13E4C5
n3:SMILES
n4:271B4F44-363D-11E5-9242-09173F13E4C5
n3:Water-Solubility
n4:271B4F3E-363D-11E5-9242-09173F13E4C5
n3:logP
n4:271B4F3F-363D-11E5-9242-09173F13E4C5 n4:271B4F3C-363D-11E5-9242-09173F13E4C5
n3:logS
n4:271B4F3D-363D-11E5-9242-09173F13E4C5
n3:pKa
n4:271B4F57-363D-11E5-9242-09173F13E4C5
n3:H-Bond-Acceptor-Count
n4:271B4F4C-363D-11E5-9242-09173F13E4C5
n3:H-Bond-Donor-Count
n4:271B4F4D-363D-11E5-9242-09173F13E4C5
n3:InChIKey
n4:271B4F47-363D-11E5-9242-09173F13E4C5
n3:Polar-Surface-Area--PSA-
n4:271B4F48-363D-11E5-9242-09173F13E4C5
n3:Polarizability
n4:271B4F4A-363D-11E5-9242-09173F13E4C5
n3:Refractivity
n4:271B4F49-363D-11E5-9242-09173F13E4C5
n3:Rotatable-Bond-Count
n4:271B4F4B-363D-11E5-9242-09173F13E4C5
n3:casRegistryNumber
61-50-7
n3:category
n3:Bioavailability
n4:271B4F52-363D-11E5-9242-09173F13E4C5
n3:Ghose-Filter
n4:271B4F54-363D-11E5-9242-09173F13E4C5
n3:MDDR-Like-Rule
n4:271B4F55-363D-11E5-9242-09173F13E4C5
n3:Melting-Point
n4:271B4F56-363D-11E5-9242-09173F13E4C5
n3:Number-of-Rings
n4:271B4F51-363D-11E5-9242-09173F13E4C5
n3:Physiological-Charge
n4:271B4F50-363D-11E5-9242-09173F13E4C5
n3:Rule-of-Five
n4:271B4F53-363D-11E5-9242-09173F13E4C5
n3:Traditional-IUPAC-Name
n4:271B4F41-363D-11E5-9242-09173F13E4C5
n3:pKa--strongest-acidic-
n4:271B4F4E-363D-11E5-9242-09173F13E4C5
n3:pKa--strongest-basic-
n4:271B4F4F-363D-11E5-9242-09173F13E4C5