MDE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C12H17NO2
Molecular Weight	207.2689
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of MDE

Structure Search

SMILES

CCNC(C)CC1=CC=C2OCOC2=C1

InChI

InChIKey=PVXVWWANJIWJOO-UHFFFAOYSA-N

InChI=1S/C12H17NO2/c1-3-13-9(2)6-10-4-5-11-12(7-10)15-8-14-11/h4-5,7,9,13H,3,6,8H2,1-2H3

HIDE SMILES / InChI

Molecular Formula	C12H17NO2
Molecular Weight	207.2689
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

Targets

Targets

Primary Target	Pharmacology	Condition	Potency
Norepinephrine transporter 197 Target ID: CHEMBL222 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22897747	Inhibitor 8504		1.02 µM [IC50]
Dopamine transporter 183 Target ID: CHEMBL238 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22897747	Inhibitor 8504		9.3 µM [IC50]
Serotonin transporter 183 Target ID: CHEMBL228 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22897747	Inhibitor 8504		1.27 µM [IC50]
Serotonin 1a (5-HT1a) receptor 177 Target ID: CHEMBL214 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22897747	Binding Agent 1076		18.8 µM [Ki]
Alpha-2a adrenergic receptor 70 Target ID: CHEMBL1867 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22897747	Binding Agent 1076		12.2 µM [Ki]

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:12:00 GMT 2025` Edited by `admin` on `Mon Mar 31 18:12:00 GMT 2025`
Record UNII	ML1I4KK67B
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

MDE

Common Name

English

MDE [MI]

Preferred Name

English

MDEA

Common Name

English

METHYLENEDIOXYETHAMPHETAMINE

Common Name

English

N-ETHYL-3,4-METHYLENEDIOXYAMPHETAMINE

Systematic Name

English

(±)-MDE

Common Name

English

(±)-N-ETHYL-3,4-METHYLENEDIOXYAMPHETAMINE

Systematic Name

English

N-ETHYL MDA

Common Name

English

(R,S)-N-ETHYL-3,4-METHYLENEDIOXYAMPHETAMINE

Systematic Name

English

3,4-METHYLENEDIOXY-N-ETHYLAMPHETAMINE

Systematic Name

English

1,3-BENZODIOXOLE-5-ETHANAMINE, N-ETHYL-.ALPHA.-METHYL-

Systematic Name

English

EVE

Common Name

English

MDE (PSYCHEDELIC)

Common Name

English

Classification Tree Code System Code

DEA NO.

7404

Created by admin on Mon Mar 31 18:12:00 GMT 2025 , Edited by admin on Mon Mar 31 18:12:00 GMT 2025

WIKIPEDIA

PiHKAL

Created by admin on Mon Mar 31 18:12:00 GMT 2025 , Edited by admin on Mon Mar 31 18:12:00 GMT 2025

Code System Code Type Description

EPA CompTox

DTXSID70860971

Created by admin on Mon Mar 31 18:12:00 GMT 2025 , Edited by admin on Mon Mar 31 18:12:00 GMT 2025

PRIMARY

INCB IDS CODE

PN 004

Created by admin on Mon Mar 31 18:12:00 GMT 2025 , Edited by admin on Mon Mar 31 18:12:00 GMT 2025

PRIMARY

PUBCHEM

105039

Created by admin on Mon Mar 31 18:12:00 GMT 2025 , Edited by admin on Mon Mar 31 18:12:00 GMT 2025

PRIMARY

MERCK INDEX

m7105

Created by admin on Mon Mar 31 18:12:00 GMT 2025 , Edited by admin on Mon Mar 31 18:12:00 GMT 2025

PRIMARY

Merck Index

FDA UNII

ML1I4KK67B

Created by admin on Mon Mar 31 18:12:00 GMT 2025 , Edited by admin on Mon Mar 31 18:12:00 GMT 2025

PRIMARY

CAS

82801-81-8

Created by admin on Mon Mar 31 18:12:00 GMT 2025 , Edited by admin on Mon Mar 31 18:12:00 GMT 2025

PRIMARY

DRUG BANK

DB01566

Created by admin on Mon Mar 31 18:12:00 GMT 2025 , Edited by admin on Mon Mar 31 18:12:00 GMT 2025

PRIMARY

WIKIPEDIA

3,4-Methylenedioxy-N-ethylamphetamine

Created by admin on Mon Mar 31 18:12:00 GMT 2025 , Edited by admin on Mon Mar 31 18:12:00 GMT 2025

PRIMARY

CHEBI

132237

Created by admin on Mon Mar 31 18:12:00 GMT 2025 , Edited by admin on Mon Mar 31 18:12:00 GMT 2025

PRIMARY

Related Record Type Details


					081I12ZA58

CYTOCHROME P450 2C19

METABOLIC ENZYME -> SUBSTRATE

Amount:


					F5C0YRV9E3

MDE HYDROCHLORIDE

SALT/SOLVATE -> PARENT

Amount:


					0UY97CSG1T

CYTOCHROME P450 2B6

METABOLIC ENZYME -> SUBSTRATE

Amount:


					JJU4XT142X

PMK METHYL GLYCIDATE

PRECURSOR->PARENT

Amount:


					23Y2GY4AJG

MDE, (S)-

ENANTIOMER -> RACEMATE

Amount:


					KE109YAK00

PIPERONAL

PRECURSOR->PARENT

Amount:


					PUO0521HZV

CYTOCHROME P450 3A4

METABOLIC ENZYME -> SUBSTRATE

Interaction Type:

MAJOR

Amount:


					8E4LAA4357

CYTOCHROME P450 2D6

METABOLIC ENZYME -> SUBSTRATE

Interaction Type:

MAJOR

Amount:


					PVK7G754HO

MDE, (R)-

ENANTIOMER -> RACEMATE

Amount:


					W6337429LF

PRECURSOR->PARENT

Amount:


					VK4SQL11C0

CYTOCHROME P450 1A2

METABOLIC ENZYME -> SUBSTRATE

Amount:


					YG6MGA6AT5

PRECURSOR->PARENT

Amount:

Related Record Type Details


					PNA80F81BT

3,4-METHYLENEDIOXYPHENYL-2-PROPANONE

METABOLITE -> PARENT

Qualification:

URINE

Amount:


					TV4TN3M5JL

3,4-METHYLENEDIOXYHIPPURIC ACID

METABOLITE -> PARENT

Qualification:

URINE

Amount:


					XJZ28FJ27W

METABOLITE -> PARENT

Amount:


					205DJY61BJ

3,4-DIHYDROXYETHYLAMPHETAMINE

METABOLITE -> PARENT

Amount:

Related Record Type Details


					ML1I4KK67B

MDE

ACTIVE MOIETY

Amount: