About: Phenylisobutylamine

Facets (new session)
Description
Metadata
Settings
- Rule:
- Inverse Functional Properties:
- "Same As":

About: Phenylisobutylamine Goto Sponge NotDistinct Permalink

An Entity of Type : umbel-rc:DrugProduct, within Data Space : dbpedia.org associated with source document(s)
QRcode icon

http://dbpedia.org/describe/?url=http%3A%2F%2Fdbpedia.org%2Fresource%2FPhenylisobutylamine

Phenylisobutylamine, also known as α-ethylphenethylamine, Butanphenamine, B or AEPEA, is a stimulant drug of the phenethylamine class. It is a higher homologue of amphetamine, differing from amphetamine's molecular structure only by the substitution of the methyl group at the alpha position of the side chain with an ethyl group. Compared to amphetamine, phenylisobutylamine has strongly reduced dopaminergic effects, and instead acts as a selective norepinephrine releasing agent. The dextroisomer of phenylisobutylamine partially substitutes for dextroamphetamine in rats.

Attributes	Values
rdf:type	Thing dul:ChemicalObject chemical substance Drug yago:WikicatAmphetamines yago:Agent114778436 yago:Amphetamine102704153 yago:CausalAgent100007347 yago:Drug103247620 yago:DrugOfAbuse103248958 yago:Matter100020827 yago:PhysicalEntity100001930 drug yago:Stimulant104320126 yago:Substance100020090 umbel-rc:DrugProduct
rdfs:label	Phenylisobutylamine (en)
rdfs:comment	Phenylisobutylamine, also known as α-ethylphenethylamine, Butanphenamine, B or AEPEA, is a stimulant drug of the phenethylamine class. It is a higher homologue of amphetamine, differing from amphetamine's molecular structure only by the substitution of the methyl group at the alpha position of the side chain with an ethyl group. Compared to amphetamine, phenylisobutylamine has strongly reduced dopaminergic effects, and instead acts as a selective norepinephrine releasing agent. The dextroisomer of phenylisobutylamine partially substitutes for dextroamphetamine in rats. (en)
foaf:depiction
dcterms:subject	Norepinephrine releasing agents
Wikipage page ID	25199081 (xsd:integer)
Wikipage revision ID	1110396226 (xsd:integer)
Link from a Wikipage to another Wikipage	4-chlorophenylisobutylamine 4-methylphenylisobutylamine Mouth Norepinephrine releasing agent Dopaminergic Norepinephrine releasing agents N,alpha-diethylphenylethylamine Functional group Stimulant Drug Amphetamine Eutylone Isobutylamine Ariadne (psychedelic) Binding selectivity Homologous series Dextroamphetamine Butylone Phenethylamine Methyl Methylbenzodioxolylbutanamine Ethyl group Side chain Alpha carbon Chemical derivative Dextroisomer Ethylbenzodioxolylbutanamine Benzodioxolylbutanamine
sameAs	Phenylisobutylamine Phenylisobutylamine Phenylisobutylamine Phenylisobutylamine Phenylisobutylamine
dbp:wikiPageUsesTemplate	dbt:Adrenergics dbt:Citation_needed dbt:Drugbox dbt:Phenethylamines dbt:Reflist dbt:Short_description dbt:Stimulants
thumbnail	wiki-commons:Special:FilePath/alpha-Ethylphenethylamine.png?width=300
ATC prefix	none (en)
c	10 (xsd:integer)
CAS number	53309 (xsd:integer)
ChemSpiderID	93687 (xsd:integer)
H	15 (xsd:integer)
IUPAC name	1 (xsd:integer)
legal DE	NpSG (en)
legal UK	Class A (en)
n	1 (xsd:integer)
PubChem	103771 (xsd:integer)
routes of administration	Mouth
SMILES	CCCN (en)
StdInChI	1 (xsd:integer)
StdInChIKey	IOLQWLOHKZENDW-UHFFFAOYSA-N (en)
has abstract	Phenylisobutylamine, also known as α-ethylphenethylamine, Butanphenamine, B or AEPEA, is a stimulant drug of the phenethylamine class. It is a higher homologue of amphetamine, differing from amphetamine's molecular structure only by the substitution of the methyl group at the alpha position of the side chain with an ethyl group. Compared to amphetamine, phenylisobutylamine has strongly reduced dopaminergic effects, and instead acts as a selective norepinephrine releasing agent. The dextroisomer of phenylisobutylamine partially substitutes for dextroamphetamine in rats. A number of derivatives of phenylisobutylamine are known, including BDB, MBDB, EBDB, butylone (βk-MBDB), eutylone (βk-EBDB), Ariadne (α-Et-DOM), 4-CAB, and 4-MAB. "Phenylisobutylamine" is in fact a chemical misnomer because isobutylamine itself contains a branched chain. The correct name after this style for this class of compound would be "phenylsecbutylamine". (en)
legal CA	Schedule I (en)
gold:hypernym	Drug
prov:wasDerivedFrom	wikipedia-en:Phenylisobutylamine?oldid=1110396226&ns=0
page length (characters) of wiki page	2726 (xsd:nonNegativeInteger)
CAS number	53309-89-0
PubChem	103771
foaf:isPrimaryTopicOf	wikipedia-en:Phenylisobutylamine
is Link from a Wikipage to another Wikipage of	N,α-Diethylphenethylamine 2-Amino-1,2-dihydronaphthalene 2-Aminotetralin 4-Chlorophenylisobutylamine 4-Methylphenylisobutylamine Monoamine releasing agent Phenyl-2-aminobutane Phenyl-2-butanamine Phenyl-2-butylamine Phenylaminobutane Phenylbutan-2-amine Phenylisobutanamine Alpha-Ethylphenethylamine Alpha-ethylphenethylamine A-Et-PEA

Faceted Search & Find service v1.17_git139 as of Feb 29 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 08.03.3330 as of Mar 19 2024, on Linux (x86_64-generic-linux-glibc212), Single-Server Edition (378 GB total memory, 59 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software