Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Xylopropamine

From Wikipedia, the free encyclopedia
Stimulant drug of the phenethylamine and amphetamine classes
Pharmaceutical compound
Xylopropamine
Clinical data
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
Identifiers
  • (±)-1-(3,4-dimethylphenyl)propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC11H17N
Molar mass163.264 g·mol−1
3D model (JSmol)
ChiralityRacemic mixture
  • c1c(ccc(c1C)C)CC(N)C
  • InChI=1S/C11H17N/c1-8-4-5-11(6-9(8)2)7-10(3)12/h4-6,10H,7,12H2,1-3H3 ☒N
  • Key:ZSZUWPRERIPUBM-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Xylopropamine (Perhedrin,Esanin), also known as3,4-dimethylamphetamine, is astimulantdrug of thephenethylamine andamphetamine classes which was developed and marketed as anappetite suppressant in the 1950s.[1]

Xylopropamine was briefly sold as thesulfatesalt, but it was not widely marketed. Other related amphetamine derivatives such as2,4-dimethylamphetamine were also investigated for the same purpose, however these drugs had negative side effects such as high blood pressure and were not very successful, mainly due to the introduction of alternative drugs likephentermine which had similar efficacy but fewer side effects.

Xylopropamine was also reported as havinganalgesic[2] andanti-inflammatory[3] effects but its side effect profile resulted in it never being further developed for these applications.

See also

[edit]

References

[edit]
  1. ^US 2384700, Schnider O, "Alkylated phenyl-isopropyl-amines and process for the manufacture of same", issued 11 September 1945, assigned to Hoffman La Roche 
  2. ^Harris SC, Worley RC (June 1957). "Analgesic properties of xylopropamine".Proceedings of the Society for Experimental Biology and Medicine.95 (2):212–5.doi:10.3181/00379727-95-23170.PMID 13441687.S2CID 34027366.
  3. ^Randall LO, Selitto JJ, Valdes J (December 1957). "Anti-inflammatory effects of xylopropamine".Archives Internationales de Pharmacodynamie et de Therapie.113 (1–2):233–49.PMID 13509788.
Adamantanes
Adenosine antagonists
Alkylamines
Ampakines
Arylcyclohexylamines
Benzazepines
Cathinones
Cholinergics
Convulsants
Eugeroics
Oxazolines
Phenethylamines
Phenylmorpholines
Piperazines
Piperidines
Phenethylpyrrolidines
Racetams
Psychedelics
Tropanes
Tryptamines
Others
Stimulants
Amphetamines and
phenethylamines
Adrenergic agonists
Other
Cannabinoid
antagonists
GLP-1,GIP,and / or
glucagon agonists
DACRAs
5-HT2C
receptor agonists
Absorption inhibitors
Uncouplers
Others
DRAsTooltip Dopamine releasing agents
NRAsTooltip Norepinephrine releasing agents
SRAsTooltip Serotonin releasing agents
Others
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
Retrieved from "https://en.wikipedia.org/w/index.php?title=Xylopropamine&oldid=1298360887"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp