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Details

Stereochemistry ACHIRAL
Molecular Formula C14H18N2O2
Molecular Weight 246.3049
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of O-ACETYLPSILOCIN

SMILES

CN(C)CCC1=CNC2=CC=CC(OC(C)=O)=C12

InChI

InChIKey=RTLRUOSYLFOFHV-UHFFFAOYSA-N
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

HIDE SMILES / InChI

Molecular Formula C14H18N2O2
Molecular Weight 246.3049
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:30:30 GMT 2023
Edited
by admin
on Sat Dec 16 10:30:30 GMT 2023
Record UNII
8BLF220HX1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
O-ACETYLPSILOCIN
Common Name English
O-ACETYL-PSILOCIN
Common Name English
4-ACO-DMT
Common Name English
PSILACETIN
Common Name English
4-ACETOXY-DMT
Common Name English
4-ACETOXY-N,N-DIMETHYLTRYPTAMINE
Systematic Name English
1H-INDOL-4-OL, 3-(2-(DIMETHYLAMINO)ETHYL)-, 4-ACETATE
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-4-AcO-DMT
Created by admin on Sat Dec 16 10:30:30 GMT 2023 , Edited by admin on Sat Dec 16 10:30:30 GMT 2023
Code System Code Type Description
WIKIPEDIA
O-ACETYLPSILOCIN
Created by admin on Sat Dec 16 10:30:30 GMT 2023 , Edited by admin on Sat Dec 16 10:30:30 GMT 2023
PRIMARY O-Acetylpsilocin (also known as psilacetin, 4-acetoxy-DMT, or 4-AcO-DMT) is a synthetically produced psychoactive drug and has been suggested by David Nichols to be a potentially useful alternative to psilocybin for pharmacological studies, as they are both believed to be prodrugs of psilocin.[3] However, some users report that O-acetylpsilocin's subjective effects differ from that of psilocybin and psilocin.[4] It is the acetylated form of the psilocybin mushroom alkaloid psilocin and is a lower homolog of 4-AcO-DET, 4-AcO-MiPT and 4-AcO-DiPT.
CAS
92292-84-7
Created by admin on Sat Dec 16 10:30:30 GMT 2023 , Edited by admin on Sat Dec 16 10:30:30 GMT 2023
PRIMARY
EVMPD
SUB183793
Created by admin on Sat Dec 16 10:30:30 GMT 2023 , Edited by admin on Sat Dec 16 10:30:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID30238955
Created by admin on Sat Dec 16 10:30:30 GMT 2023 , Edited by admin on Sat Dec 16 10:30:30 GMT 2023
PRIMARY
SMS_ID
100000169983
Created by admin on Sat Dec 16 10:30:30 GMT 2023 , Edited by admin on Sat Dec 16 10:30:30 GMT 2023
PRIMARY
PUBCHEM
15429212
Created by admin on Sat Dec 16 10:30:30 GMT 2023 , Edited by admin on Sat Dec 16 10:30:30 GMT 2023
PRIMARY
FDA UNII
8BLF220HX1
Created by admin on Sat Dec 16 10:30:30 GMT 2023 , Edited by admin on Sat Dec 16 10:30:30 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
METABOLITE ACTIVE -> PRODRUG
Related Record Type Details
ACTIVE MOIETY