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・ 2-Aminoacridine
・ 2-aminoadipate transaminase
・ 2-aminobenzenesulfonate 2,3-dioxygenase
・ 2-Aminoethoxydiphenyl borate
・ 2-aminoethylphosphonate—pyruvate transaminase
・ 2-aminohexano-6-lactam racemase
・ 2-aminohexanoate transaminase
・ 2-Aminoindane
・ 2-Aminoisobutyric acid
・ 2-aminomuconate deaminase
・ 2-Aminomuconic acid
・ 2-Aminomuconic semialdehyde
・ 2-Aminophenol
・ 2-Aminopurine
・ 2-Aminopyridine
2-Aminotetralin
・ 2-Arachidonoylglycerol
・ 2-Arachidonyl glyceryl ether
・ 2-Azetidinone
・ 2-Benzylpiperidine
・ 2-bit
・ 2-bridge knot
・ 2-Bromo-1-chloropropane
・ 2-Bromo-4,5-methylenedioxyamphetamine
・ 2-Bromo-LSD
・ 2-Bromobutane
・ 2-Bromobutyric acid
・ 2-Bromohexane
・ 2-Bromomescaline
・ 2-Bromopropane


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2-Aminotetralin : ウィキペディア英語版
2-Aminotetralin

2-Aminotetralin (2-AT), also known as 1,2,3,4-tetrahydronaphthalen-2-amine (THN), is a stimulant drug with a chemical structure consisting of a tetralin group combined with an amine.
2-AT is a rigid analogue of phenylisobutylamine and fully substitutes for d-amphetamine in rat discrimination tests, although at one eighth the potency.〔 It has been shown to inhibit the reuptake of serotonin and norepinephrine, and likely induces their release as well. It is also likely to act on dopamine on account of its full substitution of d-amphetamine in rodent studies.〔
== Chemical derivatives ==

A number of derivatives of 2-aminotetralin exist, including:

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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