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

Details

Stereochemistry ABSOLUTE
Molecular Formula C25H32N2O2
Molecular Weight 392.5338
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVOMORAMIDE

SMILES

C[C@@H](CN1CCOCC1)C(C(=O)N2CCCC2)(C3=CC=CC=C3)C4=CC=CC=C4

InChI

InChIKey=INUNXTSAACVKJS-NRFANRHFSA-N
InChI=1S/C25H32N2O2/c1-21(20-26-16-18-29-19-17-26)25(22-10-4-2-5-11-22,23-12-6-3-7-13-23)24(28)27-14-8-9-15-27/h2-7,10-13,21H,8-9,14-20H2,1H3/t21-/m0/s1

HIDE SMILES / InChI

Molecular Formula C25H32N2O2
Molecular Weight 392.5338
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Levomoramide is the levorotatory, biologically inactive isomer of dextromoramide.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Teratogenic potential of two neurotropic drugs, haloperidol and dextromoramide, tested on mouse embryos.
1990-07
[Modification, by lithium, of catalepsy induced by central cholinergic stimulants and morphine-like drugs].
1981

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:25:46 GMT 2025
Edited
by admin
on Mon Mar 31 18:25:46 GMT 2025
Record UNII
7M86YFN15D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVOMORAMIDE
INN  
INN  
Official Name English
R-898
Preferred Name English
RACEMORAMIDE, (R)-
Common Name English
(-)-4-(2-METHYL-4-OXO-3,3-DIPHENYL-4-(1-PYRROLIDINYL)BUTYL)MORPHOLINE
Systematic Name English
PYRROLIDINE, 1-(3-METHYL-4-(4-MORPHOLINYL)-1-OXO-2,2-DIPHENYLBUTYL)-, (R)-
Common Name English
levomoramide [INN]
Common Name English
PYRROLIDINE, 1-((3R)-3-METHYL-4-(4-MORPHOLINYL)-1-OXO-2,2-DIPHENYLBUTYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C67413
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
DEA NO. 9629
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
Code System Code Type Description
INN
730
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
PRIMARY
WIKIPEDIA
Levomoramide
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
PRIMARY
MESH
C018992
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
PRIMARY
PUBCHEM
10453145
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
PRIMARY
NCI_THESAURUS
C83878
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
PRIMARY
EVMPD
SUB08481MIG
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
PRIMARY
SMS_ID
100000082299
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
PRIMARY
EPA CompTox
DTXSID401016989
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
PRIMARY
ECHA (EC/EINECS)
227-123-4
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
PRIMARY
FDA UNII
7M86YFN15D
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104862
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
PRIMARY
CAS
5666-11-5
Created by admin on Mon Mar 31 18:25:46 GMT 2025 , Edited by admin on Mon Mar 31 18:25:46 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
Related Record Type Details
ACTIVE MOIETY