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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=C2C=CC=C3)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 ( + / - )

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

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:16:36 GMT 2023
Edited
by admin
on Fri Dec 15 15:16:36 GMT 2023
Record UNII
14144823D4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ALONIMID
INN   USAN  
INN   USAN  
Official Name English
2,3-DIHYDROSPIRO(NAPHTHALENE-1(4H),3'-PIPERIDINE)-2',4,6'-TRIONE
Systematic Name English
ALONIMID [USAN]
Common 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 Fri Dec 15 15:16:36 GMT 2023 , Edited by admin on Fri Dec 15 15:16:36 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C87203
Created by admin on Fri Dec 15 15:16:36 GMT 2023 , Edited by admin on Fri Dec 15 15:16:36 GMT 2023
PRIMARY
FDA UNII
14144823D4
Created by admin on Fri Dec 15 15:16:36 GMT 2023 , Edited by admin on Fri Dec 15 15:16:36 GMT 2023
PRIMARY
INN
3162
Created by admin on Fri Dec 15 15:16:36 GMT 2023 , Edited by admin on Fri Dec 15 15:16:36 GMT 2023
PRIMARY
PUBCHEM
17928
Created by admin on Fri Dec 15 15:16:36 GMT 2023 , Edited by admin on Fri Dec 15 15:16:36 GMT 2023
PRIMARY
CAS
2897-83-8
Created by admin on Fri Dec 15 15:16:36 GMT 2023 , Edited by admin on Fri Dec 15 15:16:36 GMT 2023
PRIMARY
SMS_ID
100000087465
Created by admin on Fri Dec 15 15:16:36 GMT 2023 , Edited by admin on Fri Dec 15 15:16:36 GMT 2023
PRIMARY
EVMPD
SUB05356MIG
Created by admin on Fri Dec 15 15:16:36 GMT 2023 , Edited by admin on Fri Dec 15 15:16:36 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104014
Created by admin on Fri Dec 15 15:16:36 GMT 2023 , Edited by admin on Fri Dec 15 15:16:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID00863051
Created by admin on Fri Dec 15 15:16:36 GMT 2023 , Edited by admin on Fri Dec 15 15:16:36 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY