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Details

Stereochemistry RACEMIC
Molecular Formula C13H21NO2.ClH
Molecular Weight 259.772
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DOET hydrochloride

SMILES

Cl.CCC1=CC(OC)=C(CC(C)N)C=C1OC

InChI

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

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 ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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 Fri Dec 15 15:04:35 UTC 2023
Edited
by admin
on Fri Dec 15 15:04:35 UTC 2023
Record UNII
1B7JP7F83O
Record Status Validated (UNII)
Record Version
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Name Type Language
DOET hydrochloride
Common Name English
4-ETHYL-2,5-DIMETHOXYAMPHETAMINE HYDROCHLORIDE
Systematic Name English
PHENETHYLAMINE, 4-ETHYL-2,5-DIMETHOXY-.ALPHA.-METHYL-, HYDROCHLORIDE
Common Name English
4-ETHYL-2,5-DIMETHOXY-.ALPHA.-METHYLPHENETHYLAMINE HYDROCHLORIDE
Common Name English
(±)-4-ETHYL-2,5-DIMETHOXY-.ALPHA.-METHYLPHENETHYLAMINE HYDROCHLORIDE
Common Name English
BENZENEETHANAMINE, 4-ETHYL-2,5-DIMETHOXY-.ALPHA.-METHYL-, HYDROCHLORIDE
Systematic Name English
Hecate hydrochloride
Common Name English
2,5-DIMETHOXY-4-ETHYLAMPHETAMINE HYDROCHLORIDE
Common Name English
DOET HYDROCHLORIDE (INCB:GREEN LIST)
Common Name English
DOE hydrochloride
Common Name English
BENZENEETHANAMINE, 4-ETHYL-2,5-DIMETHOXY-.ALPHA.-METHYL-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
CAS
22139-65-7
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
EPA CompTox
DTXSID00872486
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
PUBCHEM
62066
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
FDA UNII
1B7JP7F83O
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
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