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・ 5-MeO-AET
・ 5-MeO-aMT
・ 5-MeO-DALT
・ 5-MeO-DET
・ 5-MeO-DiBF
・ 5-MeO-DMT
・ 5-MeO-DPT
・ 5-MeO-EiPT
・ 5-MeO-MALT
・ 5-MeO-MiPT
・ 5-MeO-MPMI
・ 5-MeO-NBpBrT
・ 5-MeO-NMT
・ 5-MeO-pyr-T
・ 5-MeS-DMT
5-Methoxy-7,N,N-trimethyltryptamine
・ 5-Methoxy-diisopropyltryptamine
・ 5-Methoxymethylone
・ 5-Methoxysalicylic acid
・ 5-Methoxytryptamine
・ 5-Methyl-7-methoxyisoflavone
・ 5-Methyl-MDA
・ 5-Methylcytidine
・ 5-Methylcytosine
・ 5-methyldeoxycytidine-5'-phosphate kinase
・ 5-Methylethylone
・ 5-Methylindole
・ 5-methyltetrahydropteroyltriglutamate—homocysteine S-methyltransferase
・ 5-Methyluridine
・ 5-Methyluridine triphosphate


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5-Methoxy-7,N,N-trimethyltryptamine : ウィキペディア英語版
5-Methoxy-7,N,N-trimethyltryptamine

5-Methoxy-7,N,N-trimethyltryptamine (5-MeO-7,N,N-TMT, 5-MeO-7-TMT), is a tryptamine derivative which acts as an agonist at the 5-HT2 serotonin receptors.〔Benington F, Morin RD, Bradley RJ. 7-(N,N-Trimethyl)-5-methoxytryptamine. ''Journal of Heterocyclic Chemistry'' 1976; 13(4):749-751. 〕 In animal tests, both 7,N,N-TMT and 5-MeO-7,N,N-TMT produced behavioural responses similar to those of psychedelic drugs such as DMT and 5-MeO-DMT, but compounds with larger 7-position substituents such as 7-ethyl-DMT and 7-bromo-DMT did not produce psychedelic-appropriate responding despite high 5-HT2 receptor binding affinity, suggesting these may be antagonists or weak partial agonists for the 5-HT2 receptors. The related compound 7-MeO-MiPT (cf. 5-MeO-MiPT) was also found to be inactive, suggesting that the 7-position has poor tolerance for bulky groups at this position, at least if agonist activity is desired.
==See also==

* 5-MeO-2-TMT

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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