MIDOMAFETAMINE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C11H15NO2
Molecular Weight	193.2423
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of MIDOMAFETAMINE

Structure Search

SMILES

CNC(C)CC1=CC2=C(OCO2)C=C1

InChI

InChIKey=SHXWCVYOXRDMCX-UHFFFAOYSA-N

InChI=1S/C11H15NO2/c1-8(12-2)5-9-3-4-10-11(6-9)14-7-13-10/h3-4,6,8,12H,5,7H2,1-2H3

HIDE SMILES / InChI

Molecular Formula	C11H15NO2
Molecular Weight	193.2423
Charge	0
Count

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

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 17:14:56 UTC 2023` Edited by `admin` on `Sat Dec 16 17:14:56 UTC 2023`
Record UNII	KE1SEN21RM
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

MIDOMAFETAMINE

Official Name

English

midomafetamine [INN]

Common Name

English

MDMA	Locators: MI Sources:

Common Name

English

3,4-METHYLENEDIOXYMETHAMPHETAMINE

Common Name

English

(±)-N-METHYL-1-(3,4-METHYLENEDIOXYPHENYL)-2-AMINOPROPANE

Systematic Name

English

MANDY

Common Name

English

(±)-(3,4-METHYLENEDIOXY)METHAMPHETAMINE

Common Name

English

(RS)-1-(BENZO(D)(1,3)DIOXOL-5-YL)-N-METHYLPROPAN-2-AMINE

Systematic Name

English

N-METHYL-3,4-METHYLENEDIOXYAMPHETAMINE [HSDB]

Common Name

English

Midomafetamine [WHO-DD]

Common Name

English

3,4-METHYLENEDIOXYMETAMPHETAMINE

Common Name

English

METHYLENEDIOXYMETHAMFETAMINE

Common Name

English

METHYLENEDIOXYMETHAMFETAMINE [MART.]

Common Name

English

MOLLY

Common Name

English

D,L-3,4-METHYLENEDIOXYMETHAMPHETAMINE

Common Name

English

XTC

Common Name

English

METHYLENEDIOXYMETAMPHETAMINE

Common Name

English

ECSTASY

Common Name

English

1,3-BENZODIOXOLE-5-ETHANAMINE, N,.ALPHA.-DIMETHYL-

Systematic Name

English

DL-(3,4-METHYLENEDIOXY)METHAMPHETAMINE

Common Name

English

PHENETHYLAMINE, N,.ALPHA.-DIMETHYL-3,4-METHYLENEDIOXY-

Systematic Name

English

MDMA [MI]

Common Name

English

METHYLENEDIOXYMETHAMPHETAMINE

Common Name

English

(±)-N,.ALPHA.-DIMETHYL-3,4-(METHYLENEDIOXY)PHENETHYLAMINE

Systematic Name

English

MIDOMAFETAMINE [USAN]

Common Name

English

Classification Tree Code System Code

WIKIPEDIA

PiHKAL

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

NCI_THESAURUS

C47795

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

DEA NO.

7405

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

LIVERTOX

AMPHETAMINES

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

Code System Code Type Description

NCI_THESAURUS

C61081

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

INCB IDS CODE

PM 011

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

DRUG BANK

DB01454

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

HSDB

6929

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

PUBCHEM

1615

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

EPA CompTox

DTXSID90860791

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

CHEBI

1391

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

SMS_ID

100000175884

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

USAN

CD-122

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

FDA UNII

KE1SEN21RM

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

INN

10442

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

CAS

54946-52-0

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

SUPERSEDED

EVMPD

SUB20716

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

WIKIPEDIA

MDMA

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

CAS

69610-10-2

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

SUPERSEDED

CAS

42542-10-9

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

MERCK INDEX

m7106

Created by admin on Sat Dec 16 17:14:59 UTC 2023 , Edited by admin on Sat Dec 16 17:14:59 UTC 2023

PRIMARY

Merck Index

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					W6337429LF

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					0UY97CSG1T

CYTOCHROME P450 2B6

METABOLIC ENZYME -> SUBSTRATE

Interaction Type:

MAJOR

Amount:


					F202H3PMO2

SODIUM-DEPENDENT DOPAMINE TRANSPORTER

TARGET -> INHIBITOR

Amount:


					482M00274D

OCT-2

TRANSPORTER -> INHIBITOR


					HN86OLH1NW

SODIUM-DEPENDENT NORADRENALINE TRANSPORTER

TARGET -> INHIBITOR

Amount:


					PUO0521HZV

CYTOCHROME P450 3A4

METABOLIC ENZYME -> SUBSTRATE

Amount:


					081I12ZA58

CYTOCHROME P450 2C19

METABOLIC ENZYME -> SUBSTRATE

Amount:


					JJU4XT142X

PMK METHYL GLYCIDATE

PRECURSOR->PARENT

Amount:


					8E4LAA4357

CYTOCHROME P450 2D6

METABOLIC ENZYME -> SUBSTRATE

Interaction Type:

IN-VIVO

Amount:


					6G65JU3BBZ

DERIVATIVE -> PARENT

Amount:


					BSF23SJ79E

PRECURSOR->PARENT

Amount:


					4007E25Z4Z

OCT-3

TRANSPORTER -> INHIBITOR


					6AK7RRC64B

MIDOMAFETAMINE, (N-METHYL-D3)-

LABELED -> NON-LABELED

Amount:


					VK4SQL11C0

CYTOCHROME P450 1A2

METABOLIC ENZYME -> SUBSTRATE

Interaction Type:

MAJOR

Amount:


					PNA80F81BT

3,4-METHYLENEDIOXYPHENYL-2-PROPANONE

PRECURSOR->PARENT

Amount:


					KNB4E1K0AV

MIDOMAFETAMINE HYDROCHLORIDE

SALT/SOLVATE -> PARENT

Amount:


					ONY583280Z

OCT-1

TRANSPORTER -> INHIBITOR


					3947754WXW

MIDOMAFETAMINE, (R)-

ENANTIOMER -> RACEMATE

Amount:


					CJZ26L1EGI

SODIUM-DEPENDENT SEROTONIN TRANSPORTER

TARGET -> INHIBITOR

Amount:


					9B6GK297FN

MIDOMAFETAMINE, (S)-

ENANTIOMER -> RACEMATE

Amount:

Related Record Type Details


					FI7RY2GH5X

4-HYDROXY-3-METHOXYMETHAMPHETAMINE-4-O-SULFATE

METABOLITE -> PARENT

Qualification:

PLASMA

Amount:


					T0X1I0QX62

3,4-DIHYDROXYMETHAMPHETAMINE-3-O-SULFATE

METABOLITE -> PARENT

Qualification:

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Amount:


					CQZ6LFU8HQ

3,4-DIHYDROXYMETHAMPHETAMINE-4-O-SULFATE

METABOLITE -> PARENT

Qualification:

PLASMA

Amount:


					VFV03WN1VN

3,4-DIHYDROXYMETHAMPHETAMINE

METABOLITE -> PARENT

Amount:


					RBY3J6H4JW

4-HYDROXY-3-METHOXYMETHAMPHETAMINE

METABOLITE -> PARENT

Amount:


					XJZ28FJ27W

METABOLITE -> PARENT

Qualification:

PLASMA

Amount:


					WPP3V4F887

4-HYDROXY-3-METHOXYMETHAMPHETAMINE-4-BETA-D-GLUCURONIDE

METABOLITE -> PARENT

Qualification:

PLASMA

Amount:

Related Record Type Details


					KE1SEN21RM

ACTIVE MOIETY

Amount: