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・ 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
・ 2,5-Xylidine
・ 2,500 year celebration of the Persian Empire
・ 2,6-beta-fructan 6-levanbiohydrolase


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

2,5-Dimethoxy-4-isopropylamphetamine (also known as DOiP and DOiPR) 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 DOiPR as being at least an order of magnitude weaker than DOPr, with doses of 20–30 mg required to produce valid changes in mental state.
Very little data exists about the pharmacological properties, metabolism, and toxicity of DOiPR.
==See also==

* DOx

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