翻訳と辞書 ・ 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 ・ 2,6-Diaminopurine
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2,5-Dimethoxy-4-trifluoromethylamphetamine : ウィキペディア英語版 | 2,5-Dimethoxy-4-trifluoromethylamphetamine
2,5-Dimethoxy-4-trifluoromethylamphetamine (DOTFM) is a psychedelic drug of the phenethylamine and amphetamine chemical classes. It was first synthesized in 1994 by a team at Purdue University led by David E. Nichols. DOTFM is the alpha-methylated analogue of 2C-TFM, and is around twice as potent in animal studies. It acts as an agonist at the 5HT2A and 5HT2C receptors.〔 In drug-substitution experiments in rats, DOTFM fully substituted for LSD and was slightly more potent than DOI.〔 == 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-trifluoromethylamphetamine」の詳細全文を読む
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