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Details

Stereochemistry RACEMIC
Molecular Formula C25H32N2O2
Molecular Weight 392.5338
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RACEMORAMIDE

SMILES

CC(CN1CCOCC1)C(C(=O)N2CCCC2)(C3=CC=CC=C3)C4=CC=CC=C4

InChI

InChIKey=INUNXTSAACVKJS-UHFFFAOYSA-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

HIDE SMILES / InChI
Molecular Formula C25H32N2O2
Molecular Weight 392.5338
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Sat Dec 16 15:48:39 UTC 2023
Edited
by admin
on Sat Dec 16 15:48:39 UTC 2023
Record UNII
L3J8QT828G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RACEMORAMIDE
INN  
INN  
Official Name English
PYRROLIDINE, 1-(3-METHYL-4-(4-MORPHOLINYL)-1-OXO-2,2-DIPHENYLBUTYL)-, (±)-
Systematic Name English
R 610
Code English
IDS-NR-002
Code English
racemoramide [INN]
Common Name English
R-610
Code English
Classification Tree Code System Code
NCI_THESAURUS C67413
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
DEA NO. 9645
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
Code System Code Type Description
CAS
13013-15-5
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
SUPERSEDED
CHEBI
35702
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
PRIMARY
PUBCHEM
9648
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
PRIMARY
FDA UNII
L3J8QT828G
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
PRIMARY
NCI_THESAURUS
C76845
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
PRIMARY
ECHA (EC/EINECS)
208-893-0
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
PRIMARY
ChEMBL
CHEMBL431928
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
PRIMARY
INN
734
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
PRIMARY
EPA CompTox
DTXSID50859343
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
PRIMARY
SMS_ID
100000080307
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
PRIMARY
CAS
545-59-5
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
PRIMARY
EVMPD
SUB10235MIG
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
PRIMARY
WIKIPEDIA
Racemoramide
Created by admin on Sat Dec 16 15:48:40 UTC 2023 , Edited by admin on Sat Dec 16 15:48:40 UTC 2023
PRIMARY
Related Record Type Details
Structure of LEVOMORAMIDE
ENANTIOMER -> RACEMATE
Structure of DEXTROMORAMIDE
ENANTIOMER -> RACEMATE
Related Record Type Details
Structure of RACEMORAMIDE
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