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・ 4-Methylsalicylic acid
・ 4-Methylthioamphetamine
・ 4-millimeter band
・ 4-MMA
・ 4-NEMD
・ 4-Nitroaniline
・ 4-Nitrobenzaldehyde
・ 4-Nitrobenzoic acid
・ 4-Nitrocatechol 4-monooxygenase
・ 4-Nitrochlorobenzene
・ 4-Nitrophenol
・ 4-nitrophenol 2-monooxygenase
・ 4-Nitrophenol 4-monooxygenase
・ 4-Ethylmethcathinone
・ 4-Ethylphenol
4-Fluoro-5-methoxy-DMT
・ 4-Fluoro-L-threonine
・ 4-Fluoroamphetamine
・ 4-Fluorobenzoic acid
・ 4-Fluorobutyrfentanyl
・ 4-Fluoroethcathinone
・ 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


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4-Fluoro-5-methoxy-DMT : ウィキペディア英語版
4-Fluoro-5-methoxy-DMT

4-Fluoro-5-Methoxy-''N'',''N''-dimethyltryptamine (4-F-5-MeO-DMT) was first described by David E. Nichols team in 2000. It is a potent 5-HT1A agonist. Substitution with the 4-fluorine markedly increased 5-HT1A selectivity over 5-HT2A/2C receptors with potency greater than that of the 5-HT1A agonist 8-OH-DPAT.
The analog compound with the ''N'',''N''-dialkyl substituents constrained into a pyrrolidine ring, is a slightly stronger agonist for the 5-HT1A receptor and retains the selectivity over the 5-HT2A/2C receptors.
== See also ==

* 5-Fluoro-AMT
* 6-Fluoro-DMT

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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