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

Details

Stereochemistry RACEMIC
Molecular Formula C11H16N2O3S
Molecular Weight 256.321
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of OZOLINONE

SMILES

CN1C(=O)C(S\C1=C/C(O)=O)N2CCCCC2

InChI

InChIKey=NQFBZYYUAFJYNS-FPLPWBNLSA-N
InChI=1S/C11H16N2O3S/c1-12-8(7-9(14)15)17-11(10(12)16)13-5-3-2-4-6-13/h7,11H,2-6H2,1H3,(H,14,15)/b8-7-

HIDE SMILES / InChI

Molecular Formula C11H16N2O3S
Molecular Weight 256.321
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 1
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:40:49 UTC 2023
Edited
by admin
on Fri Dec 15 15:40:49 UTC 2023
Record UNII
55TIT7J81D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OZOLINONE
INN   USAN  
INN   USAN  
Official Name English
(2Z)-2-(3-METHYL-4-OXO-5-(1-PIPERIDINYL)-2-THIAZOLIDINYLIDENE)ACETIC ACID
Common Name English
ACETIC ACID, 2-(3-METHYL-4-OXO-5-(1-PIPERIDINYL)-2-THIAZOLIDINYLIDENE)-, (2Z)-
Systematic Name English
ozolinone [INN]
Common Name English
ACETIC ACID, (3-METHYL-4-OXO-5-(1-PIPERIDINYL)-2-THIAZOLIDINYLIDENE)-, (Z)-
Common Name English
(±)-OZOLINONE
Common Name English
OZOLINONE [USAN]
Common Name English
GOEDECKE-382
Code English
GOEDECKE 382
Code English
(Z)-3-METHYL-4-OXO-5-PIPERIDINO-.DELTA.(SUP 2,.ALPHA.)-THIAZOLIDINEACETIC ACID.
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C49184
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
Code System Code Type Description
CAS
56784-39-5
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
PRIMARY
PUBCHEM
6436036
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
PRIMARY
WIKIPEDIA
Ozolinone
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
PRIMARY
MESH
C018121
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
PRIMARY
ChEMBL
CHEMBL2105356
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
PRIMARY
ECHA (EC/EINECS)
260-383-7
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
PRIMARY
EVMPD
SUB09582MIG
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
PRIMARY
NCI_THESAURUS
C66289
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
PRIMARY
FDA UNII
55TIT7J81D
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
PRIMARY
SMS_ID
100000082777
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
PRIMARY
INN
3984
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
PRIMARY
EPA CompTox
DTXSID30866590
Created by admin on Fri Dec 15 15:40:49 UTC 2023 , Edited by admin on Fri Dec 15 15:40:49 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
PARENT -> METABOLITE ACTIVE
Related Record Type Details
ACTIVE MOIETY