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5-MeO-NET

From Wikipedia, the free encyclopedia
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][5] 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]

History

[edit]

5-MeO-NET was first described in thescientific literature by at least 1994.[3]

See also

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References

[edit]
  1. ^abcdeGlatfelter GC, Clark AA, Cavalco NG, Landavazo A, Partilla JS, Naeem M, Golen JA, Chadeayne AR, Manke DR, Blough BE, McCorvy JD, Baumann MH (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. ^abcdBlough 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, King A, Herrick-Davis K (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.
  5. ^Glatfelter GC, Clark AA, Cavalco NG, Landavazo A, Partilla JS, Naeem M (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.

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
Cyclized tryptamines
Isotryptamines
Related compounds
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