For faster navigation, this Iframe is preloading the Wikiwand page for 5-MeO-DMT.

5-MeO-DMT

Izvor: Wikipedija

5-MeO-DMT
(IUPAC) ime
2-(5-metoks-1H-indol-3-il)-N,N-dimetiletanamin
Klinički podaci
Identifikatori
CAS broj 1019-45-0
ATC kod nije dodeljen
PubChem[1][2] 1832
ChemSpider[3] 1766
KEGG[4] C08309 DaY
ChEBI CHEBI:2086 DaY
ChEMBL[5] CHEMBL7257 DaY
Hemijski podaci
Formula C13H18N2O 
Mol. masa 218,298 g/mol
SMILES eMolekuli & PubHem
Farmakoinformacioni podaci
Trudnoća ?
Pravni status ? (UK) Plan I(SAD)
Način primene pušenjem, uduvavanjem

5-MeO-DMT (5-metoksi-N,N-dimetiltriptamin) je moćan psihodelični triptamin. On je prisutan u širokom nizu različitih biljki i psihoaktivnih žaba. On se poput njegovih bliskih srodnika DMT i bufotenina (5-HO-DMT) od davnina koristio u Južnoj Americi kao enteogen.

Hemija

[uredi | uredi kod]

5-MeO-DMT je prvi put sintetisan 1936, i 1959. je izolovan kao jedan od psihoaktivnih sastojaka Anadenanthera peregrina semena. On se javlja u mnogim organizmima koji sadrže bufotenin (5-OH-DMT). On je O-metilni analog tog jedinjenje. 5-MeO-DMT se metaboliše prvenstveno posredstvom CYP2D6.[6]

Reference

[uredi | uredi kod]
  1. Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519.  edit
  2. Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1. 
  3. Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846.  edit
  4. Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H. 
  5. Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594.  edit
  6. Shen HW, Jiang XL, Winter JC, Yu AM. Psychedelic 5-methoxy-N,N-dimethyltryptamine: metabolism, pharmacokinetics, drug interactions, and pharmacological actions. Current Drug Metabolism. 2010 Oct;11(8):659-66. PMID 20942780

Povezano

[uredi | uredi kod]

Spoljašnje veze

[uredi | uredi kod]
Portal Medicina
Portal Hemija
{{bottomLinkPreText}} {{bottomLinkText}}
5-MeO-DMT
Listen to this article

This browser is not supported by Wikiwand :(
Wikiwand requires a browser with modern capabilities in order to provide you with the best reading experience.
Please download and use one of the following browsers:

This article was just edited, click to reload
This article has been deleted on Wikipedia (Why?)

Back to homepage

Please click Add in the dialog above
Please click Allow in the top-left corner,
then click Install Now in the dialog
Please click Open in the download dialog,
then click Install
Please click the "Downloads" icon in the Safari toolbar, open the first download in the list,
then click Install
{{::$root.activation.text}}

Install Wikiwand

Install on Chrome Install on Firefox
Don't forget to rate us

Tell your friends about Wikiwand!

Gmail Facebook Twitter Link

Enjoying Wikiwand?

Tell your friends and spread the love:
Share on Gmail Share on Facebook Share on Twitter Share on Buffer

Our magic isn't perfect

You can help our automatic cover photo selection by reporting an unsuitable photo.

This photo is visually disturbing This photo is not a good choice

Thank you for helping!


Your input will affect cover photo selection, along with input from other users.

X

Get ready for Wikiwand 2.0 🎉! the new version arrives on September 1st! Don't want to wait?