翻訳と辞書 ・ 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
・ 2,5-Xylidine
・ 2,500 year celebration of the Persian Empire
・ 2,6-beta-fructan 6-levanbiohydrolase
・ 2,6-Di-tert-butylphenol
・ 2,6-Di-tert-butylpyridine
・ 2,6-Diacetylpyridine
|
|
| 2,5-Dimethoxy-4-propylamphetamine ： ウィキペディア英語版 |
2,5-Dimethoxy-4-propylamphetamine
2,5-Dimethoxy-4-propylamphetamine (DOPR) 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''). Shulgin described DOPR is a "heavy duty psychedelic", complete with alterations of the thought process and visual distortion. Very little data exists about the pharmacological properties, metabolism, and toxicity of DOPR.
The alternative structural isomer DOIP, with a 4-isopropyl substitution, is also known but is around ten times weaker than DOPR, with an active dose of some 20-30 mg (as compared to 2-5 mg for DOPR).〔
== See also ==
* DOx
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「2,5-Dimethoxy-4-propylamphetamine」の詳細全文を読む
スポンサード リンク
| 翻訳と辞書 : 翻訳のためのインターネットリソース |
Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.
|
|