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Details

Stereochemistry RACEMIC
Molecular Formula C13H15NO2
Molecular Weight 217.2637
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLUTETHIMIDE

SMILES

CCC1(CCC(=O)NC1=O)C2=CC=CC=C2

InChI

InChIKey=JMBQKKAJIKAWKF-UHFFFAOYSA-N
InChI=1S/C13H15NO2/c1-2-13(10-6-4-3-5-7-10)9-8-11(15)14-12(13)16/h3-7H,2,8-9H2,1H3,(H,14,15,16)

HIDE SMILES / InChI

Molecular Formula C13H15NO2
Molecular Weight 217.2637
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:37:42 UTC 2023
Edited
by admin
on Fri Dec 15 15:37:42 UTC 2023
Record UNII
C8I4BVN78E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLUTETHIMIDE
HSDB   INN   JAN   MART.   MI   ORANGE BOOK   VANDF   WHO-DD  
INN  
Official Name English
GLUTETHIMIDE [MART.]
Common Name English
GLUTETHIMIDE [VANDF]
Common Name English
GLUTETHIMIDE [MI]
Common Name English
2-Ethyl-2-phenylglutarimide
Systematic Name English
DORIDEN
Brand Name English
2,6-PIPERIDINEDIONE, 3-ETHYL-3-PHENYL-
Systematic Name English
ELRODORM
Common Name English
NOXYRON
Common Name English
glutethimide [INN]
Common Name English
GLUTETHIMIDE [JAN]
Common Name English
NSC-95239
Code English
GLUTETHIMIDE [ORANGE BOOK]
Common Name English
RIGENOX
Common Name English
GLUTETHIMIDE [HSDB]
Common Name English
SARODORMIN
Common Name English
Glutethimide [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29756
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
DEA NO. 2550
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
WHO-VATC QN05CE01
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
WHO-ATC N05CE01
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
Code System Code Type Description
MESH
D005984
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
ECHA (EC/EINECS)
201-012-0
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
DRUG CENTRAL
1313
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
INN
484
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
RXCUI
4903
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY RxNorm
PUBCHEM
3487
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
SMS_ID
100000084210
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
HSDB
3088
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
ChEMBL
CHEMBL1102
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
NSC
95239
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
MERCK INDEX
m5783
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY Merck Index
FDA UNII
C8I4BVN78E
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
IUPHAR
7192
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
WIKIPEDIA
GLUTETHIMIDE
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
NCI_THESAURUS
C65807
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
EVMPD
SUB07945MIG
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
CAS
77-21-4
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
DRUG BANK
DB01437
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
EPA CompTox
DTXSID1023102
Created by admin on Fri Dec 15 15:37:43 UTC 2023 , Edited by admin on Fri Dec 15 15:37:43 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
SOLVATE->ANHYDROUS
Related Record Type Details
METABOLITE -> PARENT
URINE
METABOLITE -> PARENT
METABOLITE ACTIVE -> PARENT
PLASMA; URINE
METABOLITE TOXIC -> PARENT
Metabolite contributes to the coma produced by glutethimide overdose in man.
METABOLITE -> PARENT
URINE
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Tmax PHARMACOKINETIC ORAL ADMINISTRATION