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2C-TFM-NBOMe : ウィキペディア英語版 | 25TFM-NBOMe
25TFM-NBOMe (also known as NBOMe-2C-TFM, 2C-TFM-NBOMe, and Cimbi-138) is a derivative of the phenethylamine hallucinogen 2C-TFM, discovered in 2004 by Ralf Heim at the Free University of Berlin.〔(Ralf Heim PhD. Synthese und Pharmakologie potenter 5-HT2A-Rezeptoragonisten mit N-2-Methoxybenzyl-Partialstruktur. Entwicklung eines neuen Struktur-Wirkungskonzepts. (German) )〕 It acts as a potent partial agonist for the 5HT2A receptor, though its relative potency is disputed, with some studies finding it to be of lower potency than 25I-NBOMe,〔(Maria Silva PhD. Theoretical study of the interaction of agonists with the 5-HT2A receptor. Universität Regensburg, 2009. )〕 while others show it to be of similar or higher potency,〔 〕 possibly because of differences in the assay used.〔(Martin Hansen PhD. Design and Synthesis of Selective Serotonin Receptor Agonists for Positron Emission Tomography Imaging of the Brain. University of Copenhagen, 2011. )〕 2C-TFM-NB2OMe can be taken to produce psychedelic effects similar to 2C-I-NB2OMe and 2C-D-NB2OMe. ==See also==
* DOTFM * TFMFly * 2CBCB-NBOMe (NBOMe-TCB-2) * 2CBFly-NBOMe (NBOMe-2CB-Fly) * 25C-NBOMe (NBOMe-2CC) * 25B-NBOMe (NBOMe-2CB) * 25D-NBOMe (NBOMe-2CD) * 25I-NBOMe (NBOMe-2CI) * 25I-NBMD (NBMD-2CI) * 25B-NBOH * 25I-NBOH (NBOH-2CI) * 25I-NBF (NBF-2CI)
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