DOET

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 Search

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

Primary Target	Pharmacology	Condition	Potency
5-hydroxytryptamine receptor 2A 73 Target ID: P28223 Gene ID: 3356.0 Gene Symbol: HTR2A Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/10992048	Partial Agonist 297		137.0 nM [Ki]

PubMed

Title	Date	PubMed
Metabolic study of 2,5-dimethoxy-4-ethylamphetamine (DOET) in rats.	1975	1182040
Some pharmacological actions of 2,5-dimethoxy-4-ethylamphetamine (DOET) in rats and mice.	1975 Jan	235610
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	1197576
The discriminative stimulus properties of 2,5-dimethoxy-4-methylamphetamine (DOM): differentiation from amphetamine.	1980	6771804
Sulfur analogues of psychotomimetic agents. 2. Analogues of (2,5-dimethoxy-4-methylphenyl)-and (2,5-dimethoxy-4-ethylphenyl)isopropylamine.	1983 May	6842515
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	16867532
[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	2636911

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

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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