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5-MeO-T-NBOMe

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
5-MeO-T-NBOMe
Clinical data
Other names5MT-NBOMe; NBOMe-5-MeO-T; 5-MeO-NBOMeT;N-(2-Methoxybenzyl)-5-methoxytryptamine
Drug classSerotonin5-HT2 receptoragonist;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Identifiers
  • 2-(5-methoxy-1H-indol-3-yl)-N-[(2-methoxyphenyl)methyl]ethanamine
CAS Number
PubChemCID
ChemSpider
Chemical and physical data
FormulaC19H22N2O2
Molar mass310.397 g·mol−1
3D model (JSmol)
  • COC1=CC2=C(C=C1)NC=C2CCNCC3=CC=CC=C3OC
  • InChI=1S/C19H22N2O2/c1-22-16-7-8-18-17(11-16)14(13-21-18)9-10-20-12-15-5-3-4-6-19(15)23-2/h3-8,11,13,20-21H,9-10,12H2,1-2H3
  • Key:OROYLKZKNDLGIQ-UHFFFAOYSA-N

5-MeO-T-NBOMe, also known as5MT-NBOMe orNBOMe-5-MeO-T, is apsychedelic of thetryptamine family related to the25-NB (NBOMe) drugs.[1][2] It has been sold online as adesigner drug.[1][2]

Pharmacology

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Pharmacodynamics

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5-MeO-T-NBOMe is aserotonin5-HT2 receptoragonist and produces thehead-twitch response in rodents.[1] However, compared to25I-NBOMe, the drug is much lesspotent in producing the head-twitch response (~10-fold) and produces a much weaker maximal response (~25%).[1] 5-MeO-T-NBOMe is many times lesspotent than comparable phenethylamines such as25C-NBOMe, but is still a reasonably potent and effectivepartial agonist for the 5-HT2 family ofserotonin receptors.[1][2] A number of related compounds have also been developed, and in contrast to the phenethylamine counterparts themeta-substituted benzyl derivatives are in many cases more potent than theortho-substituted benzyl compounds.[3]

Chemistry

[edit]

Analogues of 5-MeO-T-NBOMe includeN-benzyltryptamine (NBnT),4-HO-NBnT,5-MeO-NBnT,5-MeO-NBpBrT, andNEtPhOH-THPI, among others. It also shares structural similarities withpertines likeoxypertine.

History

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5-MeO-T-NBOMe was described byDavid E. Nichols and colleagues in 2015.[1]

See also

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References

[edit]
  1. ^abcdefNichols DE, Sassano MF, Halberstadt AL, Klein LM, Brandt SD, Elliott SP, et al. (July 2015)."N-Benzyl-5-methoxytryptamines as Potent Serotonin 5-HT2 Receptor Family Agonists and Comparison with a Series of Phenethylamine Analogues".ACS Chemical Neuroscience.6 (7):1165–1175.doi:10.1021/cn500292d.PMC 4505863.PMID 25547199.
  2. ^abcToro-Sazo M, Brea J, Loza MI, Cimadevila M, Cassels BK (2019)."5-HT2 receptor binding, functional activity and selectivity in N-benzyltryptamines".PLOS ONE.14 (1) e0209804.Bibcode:2019PLoSO..1409804T.doi:10.1371/journal.pone.0209804.PMC 6328172.PMID 30629611.
  3. ^WO 2023070228A1, Bryson N, "Novel benzyltryptamine compounds", published 2023 

External links

[edit]
Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
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Tryptamines
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