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・ 2,5-diaminovalerate transaminase
・ 2,5-Dichloroaniline
・ 2,5-didehydrogluconate reductase
・ 2,5-Dihydrofuran
・ 2,5-Dihydroxy-1,4-benzoquinone
・ 2,5-Dihydroxycinnamic acid
・ 2,5-dihydroxypyridine 5,6-dioxygenase
・ 2,5-diketocamphane 1,2-monooxygenase
・ 2,5-Diketopiperazine
・ 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine
・ 2,5-Dimethoxy-4-amylamphetamine
・ 2,5-Dimethoxy-4-bromoamphetamine
・ 2,5-Dimethoxy-4-butylamphetamine
・ 2,5-Dimethoxy-4-chloroamphetamine
・ 2,5-Dimethoxy-4-ethoxyamphetamine
2,5-Dimethoxy-4-ethylamphetamine
・ 2,5-Dimethoxy-4-fluoroamphetamine
・ 2,5-Dimethoxy-4-iodoamphetamine
・ 2,5-Dimethoxy-4-isopropylamphetamine
・ 2,5-Dimethoxy-4-methylamphetamine
・ 2,5-Dimethoxy-4-nitroamphetamine
・ 2,5-Dimethoxy-4-propylamphetamine
・ 2,5-Dimethoxy-4-trifluoromethylamphetamine
・ 2,5-Dimethoxybenzaldehyde
・ 2,5-Dimethylfuran
・ 2,5-Dimethylhexane
・ 2,5-dioxopiperazine hydrolase
・ 2,5-dioxovalerate dehydrogenase
・ 2,5-Diphenyloxazole
・ 2,5-Furandicarboxylic acid


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2,5-Dimethoxy-4-ethylamphetamine : ウィキペディア英語版
2,5-Dimethoxy-4-ethylamphetamine

2,5-Dimethoxy-4-ethylamphetamine (DOET, DOE, Hecate) is a psychedelic drug of the phenethylamine and amphetamine chemical classes. It was first synthesized by Alexander Shulgin, and was described in his book ''PiHKAL'' (''Phenethylamines i Have Known And Loved'').
== Chemistry ==
DOET is in a class of compounds commonly known as substituted amphetamines; its full chemical name is 4-ethyl-2,5-dimethoxy-alpha-methylbenzeneethanamine, or 1-(2,5-dimethoxy-4-ethylphenyl)propan-2-amine. It has an active stereocenter and (R)-DOET is the more active enantiomer. DOET is an extremely rare compound and reports of its effects and toxicology in humans are sparse. However, like the more common 2,5-dimethoxy-amphetamine analogues DOB, DOI and DOM, it is a potent and long-acting psychedelic. Removal of the alpha-methyl moiety yields the 2-carbon analogue, commonly known as 2C-E, another psychedelic compound first synthesized by Dr. Alexander Shulgin.

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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