Exploring 2-AT. To explore a different substance…

Names:
2-AT · 2-Aminotetralin
IUPAC name:
1,2,3,4-Tetrahydronaphthalen-2-amine
ID: 400 · Formula: C10H13N · Molecular weight: 147.217
InChI: InChI=1S/C10H13N/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-4,10H,5-7,11H2

Glennon, RA; Liebowitz, SM. Serotonin receptor affinity of cathinone and related analogues. J. Med. Chem., 1 Jan 1982, 25 (4), 393–397. 665 kB. http://dx.doi.org/10.1021/jm00346a012

Barfknecht, CF; Nichols, DE; Rusterholz, DB; Long, JP; Engelbrecht, JA; Beaton, JM; Bradley, RJ; Dyer, DC. Potential psychotomimetics. 2-Amino-1,2,3,4-tetrahydronaphthalene analogs. J. Med. Chem., 1 Jan 1973, 16, (7), 804–808. 614 kB. http://dx.doi.org/10.1021/jm00265a013

Oberlender, R; Nichols, DE. Structural variation and (+)-amphetamine-like discriminative stimulus properties. Pharmacol. Biochem. Behav., 1 Jan 1991, 38 (3), 581–586. 586 kB. http://dx.doi.org/10.1016/0091-3057(91)90017-V

Cannon, JG; Perez, JA; Pease, JP; Long, JP; Flynn, JR; Rusterholz, DB; Dryer., SE. Comparison of biological effects of N-alkylated congeners of beta-phenethylamine derived from 2-aminotetralin, 2-aminoindan, and 6-aminobenzocycloheptene. J. Med. Chem., 1 Jan 1980, 23 (7), 745–749. 731 kB. http://dx.doi.org/10.1021/jm00181a009

Nichols, DE; Pfister, WR; Yim, GKW; Cosgrove, RJ. A new view of the structural relationship between LSD and mescaline. Brain Res. Bull., 1 May 1977, 2 (3), 169–171. 338 kB. http://dx.doi.org/10.1016/0361-9230(77)90034-X

Makriyannis, A; Bowerman, D; Sze, PY; Fournier, D; De Jong., AP. Structure activity correlations in the inhibition of brain synaptosomal 3H-norepinephrine uptake by phenethylamine analogs. The role of α-alkyl side chain and methoxyl ring substitutions. Eur. J. Pharmacol., 9 Jul 1982, 81 (2), 337–340. 313 kB. http://dx.doi.org/10.1016/0014-2999(82)90454-X

N-Methyl-2-aminotetralin
N-Ethyl-2-aminotetralin
N-Propyl-2-aminotetralin
N-Isopropyl-2-aminotetralin
N-Butyl-2-aminotetralin
N,N-Dimethyl-2-aminotetralin
N,N-Diethyl-2-aminotetralin
N,N-DIpropyl-2-aminotetralin
N,N-Dibutyl-2-aminotetralin
N-Isopropyl-N-methyl-2-aminotetralin
1451
HOT-2-AT
HHAT
1443
7-MAT
7-HAT
PCAT · 6-CAT
6-MAT
PEA
Cathinone
A · Amphetamine
α-PPP
Prolintane
α-PBP
α-PVP
2-AI
AEPEA · Phenylisobutylamine
β-Me-PEA
β-Methoxyamphetamine
Norephedrine
Phenibut
PP
BZP
1-PEA · α-PEA
Benzylamine
homo-PEA
pip-PEA
β-HO-PEA
AA
Norpseudoephedrine
Phenmetrazine
PIAP
PZAP
cPr-PEA
Phentermine
Pentorex
β-Aminoamphetamine
β-DFA
β-FA
α-FA
α-TFMA
bk-2-AT
2463
2465
2-ADN
Desoxypipradrol
Pipradrol
Desoxy-D2PM
D2PM · Diphenylprolinol
Aminorex
4-MAR · 4-Methylaminorex
MPH · Methylphenidate
EPH · Ethylphenidate
Phendimetrazine
P2P
1141
1307
1-Phenyl-2-propanol
Cyclazodone
Fenozolone
Pemoline
Thozalinone
1471
1497
1498
1499
1500
1502
1511
β,β-Me-PEA
β-iPr-PEA
DPEA
Isoethcathinone
Isopentedrone
2759
Levamisole
Homoamphetamine
α-Et-BA · 1-PPA
W-15
Phenylpropanolamine
MT-45
PV8
10825
10824
NM-2-AI
1471
2-PTC
1482
1497
1498
1500
1511
N-Methyl-2-aminotetralin
N-Ethyl-2-aminotetralin
N-Propyl-2-aminotetralin
N-Isopropyl-2-aminotetralin
N-Butyl-2-aminotetralin
N,N-Dimethyl-2-aminotetralin
N,N-Diethyl-2-aminotetralin
N,N-DIpropyl-2-aminotetralin
N,N-Dibutyl-2-aminotetralin
N-Isopropyl-N-methyl-2-aminotetralin
1451
HOT-2-AT
HHAT
1443
7-MAT
7-HAT
PCAT · 6-CAT
6-MAT
PEA
Cathinone
A · Amphetamine
α-PPP
Prolintane
α-PBP
α-PVP
2-AI
AEPEA · Phenylisobutylamine
β-Me-PEA
β-Methoxyamphetamine
Norephedrine
Phenibut
PP
BZP
1-PEA · α-PEA
Benzylamine
homo-PEA
pip-PEA
β-HO-PEA
AA
Norpseudoephedrine
Phenmetrazine
PIAP
PZAP
cPr-PEA
Phentermine
Pentorex
β-Aminoamphetamine
β-DFA
β-FA
α-FA
α-TFMA
bk-2-AT
2463
2465
2-ADN
Desoxypipradrol
Pipradrol
Desoxy-D2PM
D2PM · Diphenylprolinol
Aminorex
4-MAR · 4-Methylaminorex
MPH · Methylphenidate
EPH · Ethylphenidate
Phendimetrazine
P2P
1141
1307
1-Phenyl-2-propanol
Cyclazodone
Fenozolone
Pemoline
Thozalinone
1471
1497
1498
1499
1500
1502
1511
β,β-Me-PEA
β-iPr-PEA
DPEA
Isoethcathinone
Isopentedrone
2759
Levamisole
Homoamphetamine
α-Et-BA · 1-PPA
W-15
Phenylpropanolamine
MT-45
PV8
10825
10824
NM-2-AI
1471
2-PTC
1482
1497
1498
1500
1511
25 March 2017 · Creative Commons BY-NC-SA ·