Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

2-Amino-1,2-dihydronaphthalene

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
2-Amino-1,2-dihydronaphthalene
Clinical data
Other names2-ADN; ADN
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • 1,2-dihydronaphthalen-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC10H11N
Molar mass145.205 g·mol−1
3D model (JSmol)
  • c2ccc1c(\C=C/C(N)C1)c2
  • InChI=1S/C10H11N/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-6,10H,7,11H2 checkY
  • Key:SHLZSYAMFQNEOF-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

2-Amino-1,2-dihydronapthalene (2-ADN orADN) is astimulantdrug.[1][2] It is a rigidanalogue ofphenylisobutylamine and substitutes foramphetamine in ratdrug discrimination tests, although at approximately one-fourth thepotency.[1][2]

The drug is closely related to2-aminotetralin (2-AT; 2-amino-1,2,3,4-tetrahydronaphthalene), which also substitutes for amphetamine, and is about twice as potent as 2-AT in substituting for amphetamine.[1][2] Other homologous and rigid analogues of amphetamine besides 2-ADN and 2-AT include2-aminoindane (2-AI),1-naphthylaminopropane (1-NAP),2-naphthylaminopropane (2-NAP),1-phenylpiperazine (1-PP),6-ABTooltip 6-amino-6,7,8,9-tetrahydro-5H-benzocycloheptene, and7-ABTooltip 7-amino-6,7,8,9-tetrahydro-5H-benzocycloheptene.[3][2]

See also

[edit]

References

[edit]
  1. ^abcHathaway BA, Nichols DE, Nichols MB, Yim GK (May 1982). "A new, potent, conformationally restricted analogue of amphetamine: 2-amino-1,2-dihydronaphthalene".Journal of Medicinal Chemistry.25 (5):535–538.doi:10.1021/jm00347a011.PMID 6123601.
  2. ^abcdOberlender R, Nichols DE (March 1991)."Structural variation and (+)-amphetamine-like discriminative stimulus properties".Pharmacology, Biochemistry, and Behavior.38 (3):581–586.doi:10.1016/0091-3057(91)90017-V.PMID 2068194.S2CID 19069907.
  3. ^Glennon RA, Young R, Hauck AE, McKenney JD (December 1984). "Structure-activity studies on amphetamine analogs using drug discrimination methodology".Pharmacol Biochem Behav.21 (6):895–901.doi:10.1016/s0091-3057(84)80071-4.PMID 6522418.
Adamantanes
Adenosine antagonists
Alkylamines
Ampakines
Arylcyclohexylamines
Benzazepines
Cathinones
Cholinergics
Convulsants
Eugeroics
Oxazolines
Phenethylamines
Phenylmorpholines
Piperazines
Piperidines
Phenethylpyrrolidines
Racetams
Psychedelics
Tropanes
Tryptamines
Others
DRAsTooltip Dopamine releasing agents
NRAsTooltip Norepinephrine releasing agents
SRAsTooltip Serotonin releasing agents
Others
Retrieved from "https://en.wikipedia.org/w/index.php?title=2-Amino-1,2-dihydronaphthalene&oldid=1292749832"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp