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Details

Stereochemistry RACEMIC
Molecular Formula C13H21NO2
Molecular Weight 223.3113
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DOET

SMILES

CCC1=C(OC)C=C(CC(C)N)C(OC)=C1

InChI

InChIKey=HXJKWPGVENNMCC-UHFFFAOYSA-N
InChI=1S/C13H21NO2/c1-5-10-7-13(16-4)11(6-9(2)14)8-12(10)15-3/h7-9H,5-6,14H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C13H21NO2
Molecular Weight 223.3113
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P28223
Gene ID: 3356.0
Gene Symbol: HTR2A
Target Organism: Homo sapiens (Human)
137.0 nM [Ki]
PubMed

PubMed

TitleDatePubMed
Metabolic study of 2,5-dimethoxy-4-ethylamphetamine (DOET) in rats.
1975
Some pharmacological actions of 2,5-dimethoxy-4-ethylamphetamine (DOET) in rats and mice.
1975 Jan
The effects of 2,5-dimethoxy-4-methylamphetamine (DOM), 2,5-dimethoxy-4-ethylamphetamine (DOET), d-amphetamine, and cocaine in rats trained with mescaline as a discriminative stimulus.
1975 Oct 14
The discriminative stimulus properties of 2,5-dimethoxy-4-methylamphetamine (DOM): differentiation from amphetamine.
1980
Sulfur analogues of psychotomimetic agents. 2. Analogues of (2,5-dimethoxy-4-methylphenyl)-and (2,5-dimethoxy-4-ethylphenyl)isopropylamine.
1983 May
Optical purity determination, conformer populations and 1H NMR spectral simplification with lanthanide shift reagents--part IX. A method for improved analytical precision for "DOEt", 2,5-dimethoxy-4-ethylamphetamine.
1987
[Studies on the identification of psychotropic substances. VI. Preparation and various analytical data of reference standards of some hallucinogens, 2,5-dimethoxy-4-methylamphetamine (STP), 2,5-dimethoxy-4-bromoamphetamine (DOB) and 2,5-dimethoxy-4-ethylamphetamine (DOET)].
1989
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:31:39 GMT 2025
Edited
by admin
on Mon Mar 31 23:31:39 GMT 2025
Record UNII
9SK6K682UL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
J71.136E
Preferred Name English
DOET
Common Name English
4-ETHYL-2,5-DIMETHOXYAMPHETAMINE
Systematic Name English
HECATE
Common Name English
(±)-1-(2,5-DIMETHOXY-4-ETHYLPHENYL)-2-AMINOPROPANE
Systematic Name English
BENZENEETHANAMINE, 4-ETHYL-2,5-DIMETHOXY-.ALPHA.-METHYL-
Systematic Name English
(±)-4-ETHYL-2,5-DIMETHOXY-.ALPHA.-METHYLPHENETHYLAMINE
Systematic Name English
PHENETHYLAMINE, 4-ETHYL-2,5-DIMETHOXY-.ALPHA.-METHYL-
Systematic Name English
2,5-DIMETHOXY-4-ETHYLAMPHETAMINE
Systematic Name English
DOE
Common Name English
Classification Tree Code System Code
WIKIPEDIA PiHKAL
Created by admin on Mon Mar 31 23:31:39 GMT 2025 , Edited by admin on Mon Mar 31 23:31:39 GMT 2025
WIKIPEDIA Designer-drugs-2,5-Dimethoxy-4-ethylamphetamine
Created by admin on Mon Mar 31 23:31:39 GMT 2025 , Edited by admin on Mon Mar 31 23:31:39 GMT 2025
DEA NO. 7399
Created by admin on Mon Mar 31 23:31:39 GMT 2025 , Edited by admin on Mon Mar 31 23:31:39 GMT 2025
Code System Code Type Description
INCB IDS CODE
PD 008
Created by admin on Mon Mar 31 23:31:39 GMT 2025 , Edited by admin on Mon Mar 31 23:31:39 GMT 2025
PRIMARY
CAS
22004-32-6
Created by admin on Mon Mar 31 23:31:39 GMT 2025 , Edited by admin on Mon Mar 31 23:31:39 GMT 2025
PRIMARY
EPA CompTox
DTXSID00860585
Created by admin on Mon Mar 31 23:31:39 GMT 2025 , Edited by admin on Mon Mar 31 23:31:39 GMT 2025
PRIMARY
PUBCHEM
27402
Created by admin on Mon Mar 31 23:31:39 GMT 2025 , Edited by admin on Mon Mar 31 23:31:39 GMT 2025
PRIMARY
WIKIPEDIA
2,5-Dimethoxy-4-ethylamphetamine
Created by admin on Mon Mar 31 23:31:39 GMT 2025 , Edited by admin on Mon Mar 31 23:31:39 GMT 2025
PRIMARY
CAYMAN
11141
Created by admin on Mon Mar 31 23:31:39 GMT 2025 , Edited by admin on Mon Mar 31 23:31:39 GMT 2025
PRIMARY
DRUG BANK
DB01467
Created by admin on Mon Mar 31 23:31:39 GMT 2025 , Edited by admin on Mon Mar 31 23:31:39 GMT 2025
PRIMARY
FDA UNII
9SK6K682UL
Created by admin on Mon Mar 31 23:31:39 GMT 2025 , Edited by admin on Mon Mar 31 23:31:39 GMT 2025
PRIMARY
CAS
41538-40-3
Created by admin on Mon Mar 31 23:31:39 GMT 2025 , Edited by admin on Mon Mar 31 23:31:39 GMT 2025
SUPERSEDED
Related Record Type Details
TARGET->PARTIAL AGONIST
TARGET->PARTIAL AGONIST
SALT/SOLVATE -> PARENT
TARGET->PARTIAL AGONIST
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
TARGET -> AGONIST
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY