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

Details

Stereochemistry RACEMIC
Molecular Formula C14H13NO3
Molecular Weight 243.2579
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ALONIMID

SMILES

O=C1CCC2(CCC(=O)C3=CC=CC=C23)C(=O)N1

InChI

InChIKey=WZAIVXXKOAWTGQ-UHFFFAOYSA-N
InChI=1S/C14H13NO3/c16-11-5-7-14(8-6-12(17)15-13(14)18)10-4-2-1-3-9(10)11/h1-4H,5-8H2,(H,15,17,18)

HIDE SMILES / InChI
Molecular Formula C14H13NO3
Molecular Weight 243.2579
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description

ALONIMID, a compound which is structurally related to thalidomide, possesses sedative and hypnotic properties.

Approval Year

Unknown
149124
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:52:33 GMT 2025
Edited
by admin
on Mon Mar 31 17:52:33 GMT 2025
Record UNII
14144823D4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ALONIMID [USAN]
Preferred Name English
ALONIMID
INN   USAN  
INN   USAN  
Official Name English
2,3-DIHYDROSPIRO(NAPHTHALENE-1(4H),3'-PIPERIDINE)-2',4,6'-TRIONE
Systematic Name English
alonimid [INN]
Common Name English
SPIRO(NAPHTHALENE-1(4H),3'-PIPERIDINE)-2',4,6'-TRIONE, 2,3-DIHYDRO-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29756
Created by admin on Mon Mar 31 17:52:33 GMT 2025 , Edited by admin on Mon Mar 31 17:52:33 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C87203
Created by admin on Mon Mar 31 17:52:33 GMT 2025 , Edited by admin on Mon Mar 31 17:52:33 GMT 2025
PRIMARY
FDA UNII
14144823D4
Created by admin on Mon Mar 31 17:52:33 GMT 2025 , Edited by admin on Mon Mar 31 17:52:33 GMT 2025
PRIMARY
INN
3162
Created by admin on Mon Mar 31 17:52:33 GMT 2025 , Edited by admin on Mon Mar 31 17:52:33 GMT 2025
PRIMARY
PUBCHEM
17928
Created by admin on Mon Mar 31 17:52:33 GMT 2025 , Edited by admin on Mon Mar 31 17:52:33 GMT 2025
PRIMARY
CAS
2897-83-8
Created by admin on Mon Mar 31 17:52:33 GMT 2025 , Edited by admin on Mon Mar 31 17:52:33 GMT 2025
PRIMARY
SMS_ID
100000087465
Created by admin on Mon Mar 31 17:52:33 GMT 2025 , Edited by admin on Mon Mar 31 17:52:33 GMT 2025
PRIMARY
EVMPD
SUB05356MIG
Created by admin on Mon Mar 31 17:52:33 GMT 2025 , Edited by admin on Mon Mar 31 17:52:33 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104014
Created by admin on Mon Mar 31 17:52:33 GMT 2025 , Edited by admin on Mon Mar 31 17:52:33 GMT 2025
PRIMARY
EPA CompTox
DTXSID00863051
Created by admin on Mon Mar 31 17:52:33 GMT 2025 , Edited by admin on Mon Mar 31 17:52:33 GMT 2025
PRIMARY
Related Record Type Details
Structure of ALONIMID, (R)-
ENANTIOMER -> RACEMATE
Structure of ALONIMID, (S)-
ENANTIOMER -> RACEMATE
Related Record Type Details
Structure of ALONIMID
ACTIVE MOIETY
NIH
NCATS
PRIVACY NOTICE
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966