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・ 4-Fluoromethamphetamine
・ 4-Fluoromethylphenidate
・ 4-Fluoropethidine
・ 4-formylbenzenesulfonate dehydrogenase
・ 4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase
・ 4-H
・ 4-H Shooting Sports Programs
・ 4-Heptanone
・ 4-HO-DBT
・ 4-HO-DET
・ 4-HO-DiPT
・ 4-HO-DPT
・ 4-HO-DSBT
・ 4-HO-MET
・ 4-HO-MiPT
4-HO-MPMI
・ 4-HO-MPT
・ 4-HO-pyr-T
・ 4-HO-αMT
・ 4-HTMPIPO
・ 4-Hydroxy-2-alkylquinoline
・ 4-hydroxy-2-oxoglutarate aldolase
・ 4-Hydroxy-2-oxopentanoic acid
・ 4-hydroxy-2-oxovalerate aldolase
・ 4-Hydroxy-3-methoxymethamphetamine
・ 4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase
・ 4-Hydroxy-3-methylbut-2-enyl diphosphate reductase
・ 4-hydroxy-4-methyl-2-oxoglutarate aldolase
・ 4-Hydroxy-4-methylpentanoic acid
・ 4-Hydroxy-5-methoxydimethyltryptamine


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4-HO-MPMI : ウィキペディア英語版
4-HO-MPMI

4-HO-MPMI (also known as 4-Hydroxy-''N''-methyl-(α,''N''-trimethylene)tryptamine or lucigenol) is a tryptamine derivative that is a psychedelic drug. It was developed by the team led by David Nichols from Purdue University in the late 1990s. This compound produces hallucinogen-appropriate responding in animal tests with a similar potency to the amphetamine-derived psychedelic DOI, and has two enantiomers, with only the (''R'')-enantiomer being active.
The binding affinity for 5-HT2A receptor is 13 +/- 2 nM (Ki ()DOI). It is reported at doses starting at 0.5 mg and 1.0-1.5 mg seem to be psychedelic doses. The duration it is reported between six to eight hours. The effects, still not too documented, are OEV/CEV, sedation and anxiety.〔http://www.hipforums.com/newforums/showthread.php?t=315326〕
==See also==

* 4-HO-pyr-T
* 5-MeO-MPMI
* 5-MeO-pyr-T
* CP-135,807

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「4-HO-MPMI」の詳細全文を読む



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