O-Acetilpsilocin

O-Acetilpsilocin
(IUPAC) ime
	3-[2-(Dimetilamino)etil]-1H-indol-4-il acetat
Klinički podaci
Identifikatori
CAS broj	92292-84-7
ATC kod	nije dodeljen
PubChem	15429212
ChemSpider	21106357
Hemijski podaci
Formula	C14H18N2O2
Mol. masa	246,3049 g/mol
SMILES	eMolekuli & PubHem
InChI
	InChI=1S/C14H18N2O2/c1-10(17)18-13-6-4-5-12-14(13)11(9-15-12)7-8-16(2)3/h4-6,9,15H,7-8H2,1-3H3 ; Key: RTLRUOSYLFOFHV-UHFFFAOYSA-N
Sinonimi	4-acetoksi-N,N-dimetiltriptamin, 3-(2'-dimetilaminoetil)-4-acetoksi-indol
Fizički podaci
Tačka topljenja	172–173 °C (342–343 °F)
Farmakoinformacioni podaci
Trudnoća	?
Pravni status	? (CA) ? (SAD) ; Može se smatrati nelegalim ako je namenjen ljudskoj upotrebi
Način primene	Oralno, IV, intranazalno, rektalno

O-Acetilpsilocin (Psilacetin, 4-Acetoksi-DMT, 4-AcO-DMT) je sintetički napravljen psihoaktivni lek. On može da bude potencijalno korisna alternativa psilocibina za farmakološke studije, jer su oba molekula prolekovi psilocina.^[5] Postoji mnoštvo dokaza da se dejstvo O-acetilpsilocina znatno razlikuje od psilocibina i psilocina.^[6]

Reference

↑ 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
↑ 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.
↑ 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
↑ US patent 3075992, Šablon:Cite patent/authors, "Esters of indoles", assigned to Sandoz Ltd.
↑ Nichols, David; Fescas, Stewart (1999). „Improvements to the Synthesis of Psilocybin and a Facile Method for Preparing the O-Acetyl Prodrug of Psilocin” (PDF). Synthesis (Stuttgart · New York: Thieme) (6): 935–938. Pristupljeno 2012-01-17.
↑ http://www.erowid.org/experiences/subs/exp_4AcODMT.shtml

Spoljašnje veze

	Portal Medicina
	Portal Hemija

[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

[Esters_of_Indoles-4] US patent 3075992, Šablon:Cite patent/authors, "Esters of indoles", assigned to Sandoz Ltd.

[Nichols_1999_935–938-5] Nichols, David; Fescas, Stewart (1999). „Improvements to the Synthesis of Psilocybin and a Facile Method for Preparing the O-Acetyl Prodrug of Psilocin” (PDF). Synthesis (Stuttgart · New York: Thieme) (6): 935–938. Pristupljeno 2012-01-17.

[erowid1-6] ttp://www.erowid.org/experiences/subs/exp_4AcODMT.shtml

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