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・ 2,6-dihydroxypseudooxynicotine hydrolase
・ 2,6-Dihydroxypyridine
・ 2,6-dihydroxypyridine 3-monooxygenase
・ 2,6-Dimethoxybenzoquinone
・ 2,6-Dimethylnaphthalene
・ 2,6-Dimethylpiperidine
・ 2,6-dioxo-6-phenylhexa-3-enoate hydrolase
・ 2,6-Lutidine
・ 2,6-Naphthalenedicarboxylic acid
・ 2,6-Pyridinedicarbothioic acid
・ 2,6-Xylenol
・ 2,6-Xylidine
・ 2,7,4'-Trihydroxyisoflavanone 4'-O-methyltransferase
・ 2,7-Dihydrothiepine
・ 2,8-Dihydroxyadenine
2,alpha-DMT
・ 2,N,N-TMT
・ 2- and 4-Quinolones
・ 2-(1,2-epoxy-1,2-dihydrophenyl)acetyl-CoA isomerase
・ 2-(1-Hexyloxyethyl)-2-devinyl pyropheophorbide-a
・ 2-(2-Ethoxyethoxy)ethanol
・ 2-(2-Methoxyethoxy)ethanol
・ 2-(acetamidomethylene)succinate hydrolase
・ 2-(Dicyanomethylene)croconate
・ 2-(hydroxymethyl)-3-(acetamidomethylene)succinate hydrolase
・ 2-(R)-hydroxypropyl-CoM dehydrogenase
・ 2-(S)-hydroxypropyl-CoM dehydrogenase
・ 2-1-1
・ 2-1-2 Forecheck
・ 2-10-0


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2,alpha-DMT : ウィキペディア英語版
2,alpha-DMT

2,alpha-DMT, or 2,α-dimethyltryptamine, is a tryptamine and a lesser-known psychedelic drug. It is the 2,a-dimethyl analog of DMT. 2,α-DMT was first synthesized by Alexander Shulgin. In his book ''TiHKAL'' (''Tryptamines I Have Known and Loved''), Shulgin lists the dosage as 300-500 mg, and the duration as 7-10 hours. 2,α-DMT causes mydriasis and paresthesia. It also produces a calm, drunk-like feeling. Very little data exists about the pharmacological properties, metabolism, and toxicity of 2,α-DMT.
==References==


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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