Exploring 5-MeO-NMT. To explore a different substance…

Names:
5-MeO-NMT · N,O-DMS · nor-5-MeO-DMT · Serotonin, N,O-dimethyl · Tryptamine, 5-methoxy-N-methyl · 5-Methoxy-3-[2-(methylamino)ethyl]indole · Indole, 5-methoxy-3-[2-(methylamino)ethyl] · 5-Methoxy-N-methyltryptamine · N,O-Dimethylserotonin
IUPAC name:
2-(5-Methoxy-1H-indol-3-yl)-N-methylethan-1-amine
ID: 5042 · Formula: C12H16N2O · Molecular weight: 204.268
InChI: InChI=1S/C12H16N2O/c1-13-6-5-9-8-14-12-4-3-10(15-2)7-11(9)12/h3-4,7-8,13-14H,5-6H2,1-2H3

Blough, BE; Landavazo, A; Decker, AM; Partilla, JS; Baumann, MH; Rothman, RB. Interaction of psychoactive tryptamines with biogenic amine transporters and serotonin receptor subtypes. Psychopharmacology, 1 Oct 2014, 231 (21), 4135-4144. 298 kB. http://dx.doi.org/10.1007/s00213-014-3557-7

Jensen, N. Tryptamines as ligands and modulators of the serotonin 5-HT2A receptor and the isolation of aeruginascin from the hallucinogenic mushroom Inocybe aeruginascens. Ph. D. Thesis, Georg-August-Universität zu Göttingen, Göttingen, Germany, 4 Nov 2004. 2.3 MB. Referent: Prof. Dr. H. Laatsch; Korreferent: Prof. D. E. Nichols.

McKenna, DJ. Monoamine odixase inhibitors in Amazonian hallucinogenic plants: Ethnobotanical, phytochemical, and pharmacological investigations. Ph. D. Thesis, University of British Columbia, BC, Canada, 26 Apr 1984. 12.2 MB.

Prainer, B. Tryptamin-derivate als 5-HT4-rezeptorliganden: synthese und in-vitro-pharmakologie dissertation. Ph. D. Thesis, Universität Regensburg, Regensburg, Germany, 21 Jul 2008. 2.2 MB. In German.

Melatonin
5-MeO-DET
5-MeO-DIPT
5-MeO-DMT
5-MeO-MIPT
5-MeO-DPT
5-MeO-NCPT
5-MeO-T
N-Hexanoyl-5-MeO-T
N-Octanoyl-5-MeO-T
N-Heptafluorobutyroyl-5-MeO-T
5-MeO-DALT
5MT-NBOMe · 5MT-NB2OMe
5-MeO-EIPT
5-MeO-NALT
5-MeO-DPRT
5-MeO-MET
5MT-NB
5MT-NBOH
5MT-NB2OTFM
5MT-NB4OMe
5MT-NB4NO2
5MT-NB4NH2
5MT-NB4Me
5MT-NB4I
5-MeO-NBpBrT · 5MT-NB4B
5MT-NB4Cl
5MT-NB4F
5-MeO-NET
428
427
5-MeO-NIPT
5-MeO-MPT
5-MeO-EPT
5-MeO-DIBT
5-MeO-DBT
5-MeO-MIBT
5655
5657
5658
5659
5660
5661
5662
5663
5664
5665
5666
5667
5668
5669
5670
5671
5672
5673
5674
5675
5676
5677
5678
5679
5680
5681
5682
5683
5684
5685
5686
5687
5688
5689
5690
5691
5692
5694
5-MeO-MALT
5696
5697
5698
Methyl N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-N-methylglycinate
tert-Butyl N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-N-methylglycinate
N2-[2-(5-Methoxy-1H-indol-3-yl)ethyl]-N2-methylglycinamide
5712
5713
5MT-NB3TFM
5MT-NB3Me
5MT-NB3I
5MT-NB3Cl
5MT-NB3F
5MT-NB3B
5MT-NB2B · 5MT-NBBr
5MT-NB3OMe
5MT-NB3SMe
α,N,O-TMS
NMT
5-HO-NMT · Norbufotenine
5860
5891
5867
5866
5865
5864
5863
5862
5861
5859
5-MeO-pyr-T
5-MeO-mor-T
5-MeO-pip-T
5-MeO-MPMI
5-MeO-ICPA
5-MeO-N-Me-IPYR
5-MeO-α-MT · α,O-DMS
4-HO-DMT · Psilocin
5-HO-DMT
6-HO-DMT
7-MeO-NMT
4-MeO-NMT
7-HO-DMT
DMT N-oxide
5246
5248
4-MeO-α-MT
6-MeO-α-MT
5-EtO-T
5-MeO-2-Me-T · 2,O-DMS
Melatonin
5-MeO-DET
5-MeO-DIPT
5-MeO-DMT
5-MeO-MIPT
5-MeO-DPT
5-MeO-NCPT
5-MeO-T
N-Hexanoyl-5-MeO-T
N-Octanoyl-5-MeO-T
N-Heptafluorobutyroyl-5-MeO-T
5-MeO-DALT
5MT-NBOMe · 5MT-NB2OMe
5-MeO-EIPT
5-MeO-NALT
5-MeO-DPRT
5-MeO-MET
5MT-NB
5MT-NBOH
5MT-NB2OTFM
5MT-NB4OMe
5MT-NB4NO2
5MT-NB4NH2
5MT-NB4Me
5MT-NB4I
5-MeO-NBpBrT · 5MT-NB4B
5MT-NB4Cl
5MT-NB4F
5-MeO-NET
428
427
5-MeO-NIPT
5-MeO-MPT
5-MeO-EPT
5-MeO-DIBT
5-MeO-DBT
5-MeO-MIBT
5655
5657
5658
5659
5660
5661
5662
5663
5664
5665
5666
5667
5668
5669
5670
5671
5672
5673
5674
5675
5676
5677
5678
5679
5680
5681
5682
5683
5684
5685
5686
5687
5688
5689
5690
5691
5692
5694
5-MeO-MALT
5696
5697
5698
Methyl N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-N-methylglycinate
tert-Butyl N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-N-methylglycinate
N2-[2-(5-Methoxy-1H-indol-3-yl)ethyl]-N2-methylglycinamide
5712
5713
5MT-NB3TFM
5MT-NB3Me
5MT-NB3I
5MT-NB3Cl
5MT-NB3F
5MT-NB3B
5MT-NB2B · 5MT-NBBr
5MT-NB3OMe
5MT-NB3SMe
α,N,O-TMS
NMT
5-HO-NMT · Norbufotenine
5860
5891
5867
5866
5865
5864
5863
5862
5861
5859
5-MeO-pyr-T
5-MeO-mor-T
5-MeO-pip-T
5-MeO-MPMI
5-MeO-ICPA
5-MeO-N-Me-IPYR
5-MeO-α-MT · α,O-DMS
4-HO-DMT · Psilocin
5-HO-DMT
6-HO-DMT
7-MeO-NMT
4-MeO-NMT
7-HO-DMT
DMT N-oxide
5246
5248
4-MeO-α-MT
6-MeO-α-MT
5-EtO-T
5-MeO-2-Me-T · 2,O-DMS
30 May 2017 · Creative Commons BY-NC-SA ·