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5-MeO-NET

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
5-MeO-NET
Clinical data
Other names5-Methoxy-N-ethyltryptamine
Drug classSerotonin receptor agonist;Serotonin 5-HT2A receptor agonist;Serotonin releasing agent[1][2]
ATC code
  • None
Identifiers
  • N-ethyl-2-(5-methoxy-1H-indol-3-yl)ethan-1-amine
CAS Number
PubChemCID
ChemSpider
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H18N2O
Molar mass218.300 g·mol−1
3D model (JSmol)
  • CCNCCc1c[nH]c2c1cc(OC)cc2
  • InChI=1S/C13H18N2O/c1-3-14-7-6-10-9-15-13-5-4-11(16-2)8-12(10)13/h4-5,8-9,14-15H,3,6-7H2,1-2H3
  • Key:UNPLGMNGAFLKSH-UHFFFAOYSA-N

5-MeO-NET, also known as5-methoxy-N-ethyltryptamine, is aserotonin receptoragonist andserotonin releasing agent of thetryptamine family.[1][2][3]

Use and effects

[edit]

5-MeO-NET was not included nor mentioned inAlexander Shulgin's bookTiHKAL (Tryptamines I Have Known and Loved).[4]

Pharmacology

[edit]

Pharmacodynamics

[edit]

5-MeO-NET is apotentfull agonist or near-full agonist of theserotonin5-HT1A,5-HT2A,5-HT2B, and5-HT2C receptors.[1][2] The drug is a relatively weakserotonin releasing agent.[2]

It does not produce thehead-twitch response (HTR), a behavioral proxy ofpsychedelic effects, in rodents, suggesting that it would not behallucinogenic in humans.[1] However, 5-MeO-NET does produce the HTR if it is coadministered with a serotonin 5-HT1A receptorantagonist likeWAY-100635, suggesting that its serotonin 5-HT1A receptor agonism masks or blocks its own serotonin 5-HT2A receptor-mediated HTR induction.[1]

Chemistry

[edit]

5-MeO-NET, chemically known as 5-methoxy-N-ethyltryptamine, is a syntheticsubstituted tryptamine and aN-Ethyltryptaminederivative.

Analogues

[edit]

Analogues of 5-MeO-NET includeN-Ethyltryptamine (NET),4-HO-NET,4-AcO-NET,αET,4-HO-αET,5-MeO-αET,5-chloro-αMT (PAL-542),5-fluoro-αET (PAL-545),5-MeO-MET,5-MeO-DMT,5-MeO-DET,5-MeO-MPT,5-MeO-EPT,5-MeO-MALT, and5-MeO-MiPT, among others.[1]

History

[edit]

5-MeO-NET was first described in thescientific literature by at least 1994.[3] Research on 5-MeO-NET since the early 2000s has primarily focused on its interactions withserotonin receptors and other targets, as well as behavioral effects in rodent models.[1][2]

See also

[edit]

References

[edit]
  1. ^abcdefgGlatfelter GC, Clark AA, Cavalco NG, Landavazo A, Partilla JS, Naeem M, et al. (December 2024). "Serotonin 1A Receptors Modulate Serotonin 2A Receptor-Mediated Behavioral Effects of 5-Methoxy-N,N-dimethyltryptamine Analogs in Mice".ACS Chem Neurosci.15 (24):4458–4477.doi:10.1021/acschemneuro.4c00513.PMID 39636099.
  2. ^abcdeBlough BE, Landavazo A, Decker AM, Partilla JS, Baumann MH, Rothman RB (October 2014)."Interaction of psychoactive tryptamines with biogenic amine transporters and serotonin receptor subtypes".Psychopharmacology (Berl).231 (21):4135–4144.doi:10.1007/s00213-014-3557-7.PMC 4194234.PMID 24800892.
  3. ^abGlennon RA, Dukat M, el-Bermawy M, Law H, De los Angeles J, Teitler M, et al. (June 1994). "Influence of amine substituents on 5-HT2A versus 5-HT2C binding of phenylalkyl- and indolylalkylamines".Journal of Medicinal Chemistry.37 (13):1929–1935.doi:10.1021/jm00039a004.PMID 8027974.
  4. ^Alexander T. Shulgin,Ann Shulgin (1997).TiHKAL: The Continuation (1st ed.). Berkeley, CA: Transform Press.ISBN 978-0-9630096-9-2.OCLC 38503252. Retrieved30 January 2025.

External links

[edit]
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
DRAsTooltip Dopamine releasing agents
NRAsTooltip Norepinephrine releasing agents
SRAsTooltip Serotonin releasing agents
Others
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
α-Ketotryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
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