翻訳と辞書 ・ 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
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)』 ■ウィキペディアで「2,alpha-DMT」の詳細全文を読む
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