Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

25O-NBOMe

From Wikipedia, the free encyclopedia

Pharmaceutical compound
25O-NBOMe
Clinical data
Other names2,4,5-TMPEA-NBOMe; NBOMe-2,4,5-TMPEA; TMPEA-2-NBOMe; NBOMe-TMPEA-2;N-(2-Methoxybenzyl)-2,4,5-trimethoxyphenethylamine
Drug classSerotonin receptor modulator;Serotonin5-HT2A receptoragonist;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Identifiers
  • N-[(2-methoxyphenyl)methyl]-2-(2,4,5-trimethoxyphenyl)ethan-1-amine
PubChemCID
Chemical and physical data
FormulaC19H25NO4
Molar mass331.412 g·mol−1
3D model (JSmol)
  • COc1cc(OC)c(cc1CCNCc1ccccc1OC)OC
  • InChI=1S/C19H25NO4/c1-21-16-8-6-5-7-15(16)13-20-10-9-14-11-18(23-3)19(24-4)12-17(14)22-2/h5-8,11-12,20H,9-10,13H2,1-4H3
  • Key:YWHPPSGTTPXYSD-UHFFFAOYSA-N

25O-NBOMe, also known as2,4,5-TMPEA-NBOMe or asN-(2-methoxybenzyl)-2,4,5-trimethoxyphenethylamine, is aserotonin receptor modulator and putativepsychedelic drug of thephenethylamine and25-NB (NBOMe) families.[1][2][3] It is theN-(2-methoxybenzyl)derivative of2C-O (2,4,5-trimethoxyphenethylamine).[1][2][3]

The drug is known to act as aserotonin5-HT2A receptorpartial agonist, with anEC50Tooltip half-maximal effective concentration of 1.02 to 7.24 nM and anEmaxTooltip maximal efficacy of 57 to 129%.[1][2][3] It activated the serotonin 5-HT2A receptor with 191- to 309-fold higherpotency than 2C-Oin vitro.[3] 25O-NBOMe robustly anddose-dependently induces thehead-twitch response, a behavioral proxy of psychedelic effects, in mice, with anED50Tooltip median effective dose of 0.70 mg/kg.[3] For comparison, in other studies in mice, theED50 of25I-NBOMe was 0.078 mg/kg (9-fold lower)[4] and of25D-NBOMe was 0.23 mg/kg (3-fold lower).[5]

25O-NBOMe was first described in thescientific literature by 2009.[2] It is acontrolled substance inCanada under phenethylamine blanket-ban language.[6]

See also

[edit]

References

[edit]
  1. ^abcSilva ME, Heim R, Strasser A, Elz S, Dove S (January 2011). "Theoretical studies on the interaction of partial agonists with the 5-HT2A receptor".Journal of Computer-aided Molecular Design.25 (1):51–66.Bibcode:2011JCAMD..25...51S.doi:10.1007/s10822-010-9400-2.PMID 21088982.
  2. ^abcdSilva ME (2009).Theoretical study of the interaction of agonists with the 5-HT2A receptor (Thesis).doi:10.5283/EPUB.12119. Retrieved9 June 2025.
  3. ^abcdeWallach J, Cao AB, Calkins MM, Heim AJ, Lanham JK, Bonniwell EM, et al. (December 2023)."Identification of 5-HT2A receptor signaling pathways associated with psychedelic potential".Nature Communications.14 (1) 8221.Bibcode:2023NatCo..14.8221W.doi:10.1038/s41467-023-44016-1.PMC 10724237.PMID 38102107.
  4. ^Halberstadt AL, Geyer MA (February 2014)."Effects of the hallucinogen 2,5-dimethoxy-4-iodophenethylamine (2C-I) and superpotent N-benzyl derivatives on the head twitch response".Neuropharmacology.77:200–207.doi:10.1016/j.neuropharm.2013.08.025.PMC 3866097.PMID 24012658.
  5. ^Halberstadt AL, Chatha M, Klein AK, Wallach J, Brandt SD (May 2020)."Correlation between the potency of hallucinogens in the mouse head-twitch response assay and their behavioral and subjective effects in other species".Neuropharmacology.167 107933.doi:10.1016/j.neuropharm.2019.107933.PMC 9191653.PMID 31917152.
  6. ^"Controlled Drugs and Substances Act".Department of Justice Canada. Retrieved19 January 2026.

External links

[edit]


Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
Others
Cyclized
Bioisosteres
Phenethylamines
Scalines
2C-x
3C-x
DOx
4C-x
Ψ-PEA
MDxx
FLY
25x-NB (NBOMes)
Others
Cyclized
Lysergamides
Others
Natural sources
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds


Stub icon

Thishallucinogen-related article is astub. You can help Wikipedia byadding missing information.

Retrieved from "https://en.wikipedia.org/w/index.php?title=25O-NBOMe&oldid=1333815893"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2026 Movatter.jp