ETHYLONE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C12H15NO3
Molecular Weight	221.2524
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of ETHYLONE

Structure Search

SMILES

CCNC(C)C(=O)C1=CC2=C(OCO2)C=C1

InChI

InChIKey=MJEMIOXXNCZZFK-UHFFFAOYSA-N

InChI=1S/C12H15NO3/c1-3-13-8(2)12(14)9-4-5-10-11(6-9)16-7-15-10/h4-6,8,13H,3,7H2,1-2H3

HIDE SMILES / InChI

Molecular Formula	C12H15NO3
Molecular Weight	221.2524
Charge	0
Count

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

Approval Year

PubMed

PubMed

Title	Date	PubMed
Determination of the metabolites of the new designer drugs bk-MBDB and bk-MDEA in human urine.	2009 Jul 1	19406592
Metabolism of designer drugs of abuse: an updated review.	2010 Jun 1	20540700

Patents

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 10:14:47 GMT 2023` Edited by `admin` on `Sat Dec 16 10:14:47 GMT 2023`
Record UNII	L91C78FW96
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

ETHYLONE

Common Name

English

1-PROPANONE, 1-(1,3-BENZODIOXOL-5-YL)-2-(ETHYLAMINO)-

Systematic Name

English

BK-MDEA

Common Name

English

2-ETHYLAMINO-1-(3,4-METHYLENEDIOXYPHENYL)PROPAN-1-ONE

Systematic Name

English

1-(1,3-BENZODIOXOL-5-YL)-2-(ETHYLAMINO)PROPAN-1-ONE

Common Name

English

3,4-METHYLENEDIOXY-N-ETHYLCATHINONE

Common Name

English

BK-MDE

Common Name

English

1-(BENZO(D)(1,3)DIOXOL-5-YL)-2-(ETHYLAMINO)PROPAN-1-ONE

Systematic Name

English

J2.528.311B

Code

English

MDEC

Common Name

English

Classification Tree Code System Code

WIKIPEDIA

Designer-drugs-Ethylone

Created by admin on Sat Dec 16 10:14:47 GMT 2023 , Edited by admin on Sat Dec 16 10:14:47 GMT 2023

DEA NO.

7547

Created by admin on Sat Dec 16 10:14:47 GMT 2023 , Edited by admin on Sat Dec 16 10:14:47 GMT 2023

Code System Code Type Description

PUBCHEM

57252245

Created by admin on Sat Dec 16 10:14:47 GMT 2023 , Edited by admin on Sat Dec 16 10:14:47 GMT 2023

PRIMARY

EVMPD

SUB179033

Created by admin on Sat Dec 16 10:14:47 GMT 2023 , Edited by admin on Sat Dec 16 10:14:47 GMT 2023

PRIMARY

SMS_ID

100000164556

Created by admin on Sat Dec 16 10:14:47 GMT 2023 , Edited by admin on Sat Dec 16 10:14:47 GMT 2023

PRIMARY

WIKIPEDIA

ETHYLONE

Created by admin on Sat Dec 16 10:14:47 GMT 2023 , Edited by admin on Sat Dec 16 10:14:47 GMT 2023

PRIMARY

CAS

1112937-64-0

Created by admin on Sat Dec 16 10:14:47 GMT 2023 , Edited by admin on Sat Dec 16 10:14:47 GMT 2023

PRIMARY

EPA CompTox

DTXSID20894842

Created by admin on Sat Dec 16 10:14:47 GMT 2023 , Edited by admin on Sat Dec 16 10:14:47 GMT 2023

PRIMARY

FDA UNII

L91C78FW96

Created by admin on Sat Dec 16 10:14:47 GMT 2023 , Edited by admin on Sat Dec 16 10:14:47 GMT 2023

PRIMARY

Related Record Type Details


					01S427WO5V

METABOLITE -> PARENT

Comments:

abuser A: 0.96 (30, after hydrolysis) mcg/mL; abuser B: N.D. (1.6, after hydrolysis) mcg/mL

Interaction Type:

IN-VIVO

Qualification:

URINE


					K0XHQ9FYT3

BK-MDA

METABOLITE -> PARENT

Comments:

abuser A: 0.28 (0.23, after hydrolysis) mcg/mL; abuser B: not quantitated

Interaction Type:

IN-VIVO

Qualification:

URINE


					M0Q623MM1W

METABOLITE -> PARENT

Comments:

abuser A: N.D. (10, after hydrolysis) mcg/mL; abuser B: N.D. (0.49, after hydrolysis) mcg/mL

Interaction Type:

IN-VIVO

Qualification:

URINE


					29HPR92AIB

2-ETHYLAMINO-1-(3,4-METHYLENEDIOXYPHENYL)PROPAN-1-OL

METABOLITE -> PARENT

Comments:

abuser A: 19[42*] (23[43*], after hydrolysis) msg/mL; abuser B: 0.25[2.6*] (0.18[2.5*], after hydrolysis) mcg/mL; *diastereomer

Interaction Type:

IN-VIVO

Qualification:

URINE


					LF4AO9N378

1-(3,4-DIHYDROXYPHENYL)-2-(ETHYLAMINO)-1-PROPANONE

METABOLITE -> PARENT

Qualification:

URINE

Related Record Type Details


					L91C78FW96

ETHYLONE

ACTIVE MOIETY