U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C23H31NO2
Molecular Weight 353.4977
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVOMETHADYL ACETATE

SMILES

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

InChI

InChIKey=XBMIVRRWGCYBTQ-AVRDEDQJSA-N
InChI=1S/C23H31NO2/c1-6-22(26-19(3)25)23(17-18(2)24(4)5,20-13-9-7-10-14-20)21-15-11-8-12-16-21/h7-16,18,22H,6,17H2,1-5H3/t18-,22-/m0/s1

HIDE SMILES / InChI

Molecular Formula C23H31NO2
Molecular Weight 353.4977
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:02:38 UTC 2023
Edited
by admin
on Sat Dec 16 17:02:38 UTC 2023
Record UNII
R3B637Y991
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVOMETHADYL ACETATE
MI   USAN  
USAN  
Official Name English
(-)-6-(DIMETHYLAMINO)-4,4-DIPHENYL-3-HEPTANOL ACETATE (ESTER)
Common Name English
LAAM
Code English
levacetylmethadol [INN]
Common Name English
LEVOACETYL METHADOL
Common Name English
(1S,4S)-(6-DIMETHYLAMINO-4,4-DIPHENYL-HEPTAN-3-YL) ACETATE
Common Name English
LAA-M
Code English
LEVACETYLMETHADOL [EMA EPAR]
Common Name English
LEVACETYLMETHADOL
EMA EPAR   INN   MART.   WHO-DD  
INN  
Official Name English
LEVOMETHADYL ACETATE [USAN]
Common Name English
LEVACETYLMETHADOL [MART.]
Common Name English
Levacetylmethadol [WHO-DD]
Common Name English
BENZENEETHANOL, .BETA.-(2-(DIMETHYLAMINO)PROPYL)-.ALPHA.-ETHYL-.BETA.-PHENYL-, ACETATE (ESTER), (-)-
Common Name English
LEVOMETHADYL ACETATE [MI]
Common Name English
LEVO-ALPHACETYLMETHADOL
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C67413
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
EMA ASSESSMENT REPORTS ORLAAM (WITHDRAWN: OPIOID-RELATED DISORDERS)
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
WHO-ATC N07BC03
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
DEA NO. 9648
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
WHO-VATC QN07BC03
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
Code System Code Type Description
EVMPD
SUB08451MIG
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
MERCK INDEX
m6789
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY Merck Index
WIKIPEDIA
LEVACETYLMETHADOL
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
ChEMBL
CHEMBL1514
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
FDA UNII
R3B637Y991
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
NCI_THESAURUS
C87359
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
DRUG CENTRAL
1571
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
EPA CompTox
DTXSID3023211
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
PUBCHEM
15130
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
CAS
1477-40-3
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
SMS_ID
100000085464
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
INN
3175
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
DRUG BANK
DB01227
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
CAS
34433-66-4
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
SUPERSEDED
CHEBI
6441
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
IUPHAR
7212
Created by admin on Sat Dec 16 17:02:38 UTC 2023 , Edited by admin on Sat Dec 16 17:02:38 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY