LEVOMETHADONE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C21H27NO
Molecular Weight	309.4452
Optical Activity	( - )
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of LEVOMETHADONE

Structure Search

SMILES

CCC(=O)C(C[C@@H](C)N(C)C)(C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=USSIQXCVUWKGNF-QGZVFWFLSA-N

InChI=1S/C21H27NO/c1-5-20(23)21(16-17(2)22(3)4,18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6-15,17H,5,16H2,1-4H3/t17-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C21H27NO
Molecular Weight	309.4452
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	1 / 1
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 18:03:48 UTC 2023` Edited by `admin` on `Fri Dec 15 18:03:48 UTC 2023`
Record UNII	6Y75Z4E8NS
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

LEVOMETHADONE

Official Name

English

LEVADONE

Common Name

English

L-POLAMIVET

Common Name

English

(6R)-6-(DIMETHYLAMINO)-4,4-DIPHENYL-3-HEPTANONE

Systematic Name

English

D-(-)-METHADONE

Common Name

English

(R)-METHADONE

Common Name

English

R-(-)-METHADONE

Common Name

English

METHADONE, L-

Common Name

English

(6R)-METHADONE

Common Name

English

HEPTANONE, 6-(DIMETHYLAMINO)-4,4-DIPHENYL-, L-

Common Name

English

(-)-METHADONE

Common Name

English

LEVOTHYL

Brand Name

English

(-)-(R)-6-(DIMETHYLAMINO)-4,4-DIPHENYL-3-HEPTANONE

Systematic Name

English

3-HEPTANONE, 6-(DIMETHYLAMINO)-4,4-DIPHENYL-, (R)-

Systematic Name

English

3-HEPTANONE, 6-(DIMETHYLAMINO)-4,4-DIPHENYL-, (6R)-

Systematic Name

English

L-METHADONE

Common Name

English

Levomethadone [WHO-DD]

Common Name

English

levomethadone [INN]

Common Name

English

Classification Tree Code System Code

WHO-ATC

N07BC05

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

WHO-VATC

QN07BC05

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

Code System Code Type Description

CAS

3861-94-7

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

SUPERSEDED

CAS

52310-03-9

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

SUPERSEDED

CHEBI

136003

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

PRIMARY

WIKIPEDIA

Levomethadone

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

PRIMARY

NCI_THESAURUS

C166969

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

PRIMARY

DRUG CENTRAL

4586

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

PRIMARY

EVMPD

SUB08477MIG

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

PRIMARY

PUBCHEM

22267

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

PRIMARY

RXCUI

236913

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

PRIMARY

RxNorm

DRUG BANK

DB13515

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

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CAS

125-58-6

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

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SMS_ID

100000082297

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

PRIMARY

EPA CompTox

DTXSID70101637

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

PRIMARY

ChEMBL

CHEMBL159659

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

PRIMARY

INN

5002

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

PRIMARY

FDA UNII

6Y75Z4E8NS

Created by admin on Fri Dec 15 18:03:48 UTC 2023 , Edited by admin on Fri Dec 15 18:03:48 UTC 2023

PRIMARY

Related Record Type Details


					V57LC776C0

LEVOMETHADONE HYDROCHLORIDE

SALT/SOLVATE -> PARENT


					UC6VBE7V1Z

METHADONE

RACEMATE -> ACTIVE ENANTIOMER

Comments:

approximately 50x the potency of the S-(+)-enantiomer as well as greater μ-opioid receptor selectivity


					S95RZH8AMH

ENANTIOMER -> ENANTIOMER

Amount:


					482M00274D

OCT-2

TRANSPORTER -> INHIBITOR

Related Record Type Details


					6Y75Z4E8NS

ACTIVE MOIETY