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N-Ethyltryptamine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
N-Ethyltryptamine
Clinical data
Other namesNET; NETP; Ethyltryptamine
ATC code
  • None
Legal status
Legal status
Identifiers
  • N-ethyl-2-(1H-indol-3-yl)ethan-1-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC12H16N2
Molar mass188.274 g·mol−1
3D model (JSmol)
Melting point87 to 88 °C (189 to 190 °F)
  • CCNCCc1c[nH]c2ccccc12
  • InChI=1S/C12H16N2/c1-2-13-8-7-10-9-14-12-6-4-3-5-11(10)12/h3-6,9,13-14H,2,7-8H2,1H3 checkY
  • Key:TZWUSTVNAVKAPA-UHFFFAOYSA-N checkY
  (verify)

N-Ethyltryptamine (NET), also abbreviated asNETP, is atryptamine that isstructurally related toN-methyltryptamine (NMT) and thepsychedelic drugsN,N-dimethyltryptamine (DMT) andN,N-diethyltryptamine (DET).[1]

Use and effects

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Alexander Shulgin included NET as an entry in his bookTiHKAL (Tryptamines I Have Known and Loved).[1] However, he stated that it had been subjected only to modest human trials and that no active dose level had been identified.[1]

Pharmacology

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Pharmacodynamics

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NMT activities
TargetAffinity (Ki, nM)
5-HT1AIA
5-HT2A38 (EC50Tooltip half-maximal effective concentration)
99% (EmaxTooltip maximal efficacy)
SERT19a (EC50)
NETTooltip Norepinephrine transporter3,862a (EC50)
DATTooltip Dopamine transporter6,660a (EC50)
Notes: The smaller the value, the more avidly the drug interacts with the site.Footnotes:a =Neurotransmitter release.Sources:[2]

NET has been found to act as apotentserotonin5-HT2A receptorfull agonist and a selectiveserotonin releasing agent.[2] It is inactive at the5-HT1A receptor.[2]

Chemistry

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Synthesis

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Thechemical synthesis of NET has been described.[1]

Analogues

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Analogues of NET includeN-methyltryptamine (NMT),dimethyltryptamine (DMT),methylethyltryptamine (MET), anddiethyltryptamine (DET), among others.[1]

See also

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References

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  1. ^abcdeNET Entry inTIHKAL
  2. ^abcBlough 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.

External links

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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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