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
[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 Fri Dec 15 16:21:04 GMT 2023
Edited
by admin
on Fri Dec 15 16:21:04 GMT 2023
Record UNII
7M86YFN15D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVOMORAMIDE
INN  
INN  
Official 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
R-898
Code English
Classification Tree Code System Code
NCI_THESAURUS C67413
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
DEA NO. 9629
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
Code System Code Type Description
INN
730
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
PRIMARY
WIKIPEDIA
Levomoramide
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
PRIMARY
MESH
C018992
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
PRIMARY
PUBCHEM
10453145
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
PRIMARY
NCI_THESAURUS
C83878
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
PRIMARY
EVMPD
SUB08481MIG
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
PRIMARY
SMS_ID
100000082299
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
PRIMARY
EPA CompTox
DTXSID401016989
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
PRIMARY
ECHA (EC/EINECS)
227-123-4
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
PRIMARY
FDA UNII
7M86YFN15D
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104862
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
PRIMARY
CAS
5666-11-5
Created by admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
Related Record Type Details
ACTIVE MOIETY