Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

EMDT

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
EMDT
Clinical data
Other names2-Ethyl-5-methoxy-N,N-dimethyltryptamine; 2-Ethyl-5-MeO-DMT; 2-Et-5-MeO-DMT
ATC code
  • none
Identifiers
  • 2-(2-ethyl-5-methoxy-1H-indol-3-yl)-N,N-dimethylethanamine
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC15H22N2O
Molar mass246.354 g·mol−1
3D model (JSmol)
  • CCc2[nH]c1ccc(OC)cc1c2CCN(C)C
  • InChI=1S/C15H22N2O/c1-5-14-12(8-9-17(2)3)13-10-11(18-4)6-7-15(13)16-14/h6-7,10,16H,5,8-9H2,1-4H3 ☒N
  • Key:ZEYRDXUWJDGTLD-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

2-Ethyl-5-methoxy-N,N-dimethyltryptamine (EMDT), also known as2-ethyl-5-MeO-DMT, is atryptamine derivative which is used inscientific research. It acts as aselective5-HT6 receptoragonist, with aKi of 16 nM, and was one of the first selective agonists developed for this receptor.[1][2] Itsaffinities for many othertargets have also been reported.[2] EMDT inhibits bothshort- andlong-term memory formation in animal studies, and this effect can be reversed by the selective 5-HT6 antagonistSB-399,885.[3] Additionally, it is active in thetail suspension test, suggesting that it could be an effectiveantidepressant.[4]

See also

[edit]

References

[edit]
  1. ^Glennon RA, Lee M, Rangisetty JB, Dukat M,Roth BL, Savage JE, et al. (March 2000). "2-Substituted tryptamines: agents with selectivity for 5-HT(6) serotonin receptors".Journal of Medicinal Chemistry.43 (5):1011–1018.doi:10.1021/jm990550b.PMID 10715164.
  2. ^abRay TS (February 2010)."Psychedelics and the human receptorome".PLOS ONE.5 (2) e9019.Bibcode:2010PLoSO...5.9019R.doi:10.1371/journal.pone.0009019.PMC 2814854.PMID 20126400.
  3. ^Meneses A, Perez-Garcia G, Liy-Salmeron G, Flores-Galvez D, Castillo C, Castillo E (December 2008). "The effects of the 5-HT(6) receptor agonist EMD and the 5-HT(7) receptor agonist AS19 on memory formation".Behavioural Brain Research.195 (1):112–119.doi:10.1016/j.bbr.2007.11.023.PMID 18191236.S2CID 144901859.
  4. ^Svenningsson P, Tzavara ET, Qi H, Carruthers R, Witkin JM, Nomikos GG, Greengard P (April 2007)."Biochemical and behavioral evidence for antidepressant-like effects of 5-HT6 receptor stimulation".The Journal of Neuroscience.27 (15):4201–4209.doi:10.1523/JNEUROSCI.3110-06.2007.PMC 6672541.PMID 17428998.
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
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
Retrieved from "https://en.wikipedia.org/w/index.php?title=EMDT&oldid=1323862185"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp