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Namespace Prefixes

PrefixIRI
n2http://linked.opendata.cz/resource/drugbank/drug/
dctermshttp://purl.org/dc/terms/
n14http://linked.opendata.cz/resource/drugbank/drug/DB06690/identifier/kegg-drug/
n9http://linked.opendata.cz/resource/drugbank/drug/DB06690/identifier/drugbank/
n5http://linked.opendata.cz/resource/drugbank/dosage/
n11http://linked.opendata.cz/resource/drugbank/mixture/
n7http://bio2rdf.org/drugbank:
admshttp://www.w3.org/ns/adms#
n12http://linked.opendata.cz/resource/drugbank/drug/DB06690/identifier/chemspider/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
n3http://linked.opendata.cz/ontology/drugbank/
n4http://linked.opendata.cz/resource/drugbank/property/
n13http://linked.opendata.cz/resource/drugbank/drug/DB06690/identifier/wikipedia/
xsdhhttp://www.w3.org/2001/XMLSchema#
n10http://linked.opendata.cz/resource/drugbank/drug/DB06690/identifier/kegg-compound/
n16http://linked.opendata.cz/ontology/sukl/drug/
n17http://linked.opendata.cz/resource/atc/
n15http://linked.opendata.cz/resource/drugbank/drug/DB06690/identifier/pubchem-compound/

Statements

Subject Item
n2:DB06690
rdf:type
n3:Drug
n3:description
Nitrous oxide, commonly known as "laughing gas", is a chemical compound with the chemical formula N2O. At room temperature, it is a colorless non-flammable gas, with a pleasant, slightly sweet odor and taste. It is used in surgery and dentistry for its anesthetic and analgesic effects. It is known as "laughing gas" due to the euphoric effects of inhaling it, a property that has led to its recreational use as an inhalant drug [Wikipedia].
n3:dosage
n5:271B4E33-363D-11E5-9242-09173F13E4C5 n5:271B4E34-363D-11E5-9242-09173F13E4C5 n5:271B4E35-363D-11E5-9242-09173F13E4C5 n5:271B4E36-363D-11E5-9242-09173F13E4C5
n3:group
approved
owl:sameAs
n7:DB06690
dcterms:title
Nitrous oxide
adms:identifier
n9:DB06690 n10:C00887 n12:923 n13:Nitrous_oxide n14:D00102 n15:948
n3:mechanismOfAction
Findings to date indicate that nitrous oxide induces opioid peptide release in the brain stem leading to the activation of descending noradrenergic neurones, which results in modulation of the nociceptive process in the spinal cord. Several receptor–effector mechanisms including dopamine receptors, α2 adrenoceptors, benzodiazepine receptors and -methyl- -aspartate (NMDA) receptors have been implicated although the relationship of one with the other is not known.
n3:mixture
n11:271B4E32-363D-11E5-9242-09173F13E4C5
n3:IUPAC-Name
n4:271B4E38-363D-11E5-9242-09173F13E4C5
n3:InChI
n4:271B4E3E-363D-11E5-9242-09173F13E4C5
n3:Molecular-Formula
n4:271B4E3D-363D-11E5-9242-09173F13E4C5
n3:Molecular-Weight
n4:271B4E3A-363D-11E5-9242-09173F13E4C5
n3:Monoisotopic-Weight
n4:271B4E3B-363D-11E5-9242-09173F13E4C5
n3:SMILES
n4:271B4E3C-363D-11E5-9242-09173F13E4C5
n3:logP
n4:271B4E4F-363D-11E5-9242-09173F13E4C5 n4:271B4E37-363D-11E5-9242-09173F13E4C5
n16:hasATCCode
n17:N01AX13
n3:H-Bond-Acceptor-Count
n4:271B4E44-363D-11E5-9242-09173F13E4C5
n3:H-Bond-Donor-Count
n4:271B4E45-363D-11E5-9242-09173F13E4C5
n3:InChIKey
n4:271B4E3F-363D-11E5-9242-09173F13E4C5
n3:Polar-Surface-Area--PSA-
n4:271B4E40-363D-11E5-9242-09173F13E4C5
n3:Polarizability
n4:271B4E42-363D-11E5-9242-09173F13E4C5
n3:Refractivity
n4:271B4E41-363D-11E5-9242-09173F13E4C5
n3:Rotatable-Bond-Count
n4:271B4E43-363D-11E5-9242-09173F13E4C5
n3:casRegistryNumber
10024-97-2
n3:Bioavailability
n4:271B4E49-363D-11E5-9242-09173F13E4C5
n3:Boiling-Point
n4:271B4E4E-363D-11E5-9242-09173F13E4C5
n3:Ghose-Filter
n4:271B4E4B-363D-11E5-9242-09173F13E4C5
n3:MDDR-Like-Rule
n4:271B4E4C-363D-11E5-9242-09173F13E4C5
n3:Melting-Point
n4:271B4E4D-363D-11E5-9242-09173F13E4C5
n3:Number-of-Rings
n4:271B4E48-363D-11E5-9242-09173F13E4C5
n3:Physiological-Charge
n4:271B4E47-363D-11E5-9242-09173F13E4C5
n3:Rule-of-Five
n4:271B4E4A-363D-11E5-9242-09173F13E4C5
n3:Traditional-IUPAC-Name
n4:271B4E39-363D-11E5-9242-09173F13E4C5
n3:pKa--strongest-basic-
n4:271B4E46-363D-11E5-9242-09173F13E4C5