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Details

Stereochemistry RACEMIC
Molecular Formula C10H16N2OS
Molecular Weight 212.312
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ALBUTOIN

SMILES

CC(C)CC1NC(=S)N(CC=C)C1=O

InChI

InChIKey=RATGSRSDPNECNO-UHFFFAOYSA-N
InChI=1S/C10H16N2OS/c1-4-5-12-9(13)8(6-7(2)3)11-10(12)14/h4,7-8H,1,5-6H2,2-3H3,(H,11,14)

HIDE SMILES / InChI

Molecular Formula C10H16N2OS
Molecular Weight 212.312
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Albutoin has been shown to have an anticonvulsant activity against clonic and tonic experimental seizures in mice and rats, particularly those induced by pentylenetetrazol. The first report, in 1959, of the clinical use of albutoin indicated that the drug was more effective in tonic-clonic seizures than in absence seizures. Albutoin was marketed in Europe as CO-ORD and Euprax by Baxter Laboratories. Albutoin was not approved by the United States Food and Drug Administration.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacologic interactions of albutoin with other anticonvulsant drugs.
1970 Aug
Evaluation of albutoin as an antiepileptic drug.
1974 Apr
Drug treatment of epilepsy in the century of the ILAE: the second 50 years, 1959-2009.
2009 Mar

Sample Use Guides

The low dosage of albutoin (600 mg/day, medication schedule 2) was not more effective than placebo (medication schedule 1) in preventing excess seizures. The high dosage of albutoin (1,200 mg/day, medication schedule 3) had about the same effectiveness as the low dosage of phenobarbital (150 mg/day, medication schedule 4) in preventing excess seizures.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:54:41 GMT 2023
Edited
by admin
on Sat Dec 16 16:54:41 GMT 2023
Record UNII
475NGR2DC1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ALBUTOIN
INN   MART.   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
ALBUTOIN [MART.]
Common Name English
(±)-4-IMIDAZOLIDINONE, 5-(2-METHYLPROPYL)-3-(2-PROPENYL)-2-THIOXO-
Systematic Name English
4-IMIDAZOLIDINONE, 5-(2-METHYLPROPYL)-3-(2-PROPENYL)-2-THIOXO-
Systematic Name English
Albutoin [WHO-DD]
Common Name English
ALBUTOIN [MI]
Common Name English
BAX-422Z
Code English
ALBUTOIN [USAN]
Common Name English
3-Allyl-5-isobutyl-2-thiohydantoin
Systematic Name English
EUPRAX
Brand Name English
albutoin [INN]
Common Name English
(±)-3-ALLYL-5-ISOBUTYL-2-THIOHYDANTOIN
Systematic Name English
BAX 422Z
Code English
Classification Tree Code System Code
NCI_THESAURUS C264
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL327235
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY
PUBCHEM
3032361
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY
CAS
830-89-7
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY
EVMPD
SUB05298MIG
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY
INN
1449
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY
MERCK INDEX
m1481
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY Merck Index
DRUG CENTRAL
106
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY
EPA CompTox
DTXSID0022565
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY
NCI_THESAURUS
C90706
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY
FDA UNII
475NGR2DC1
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY
MESH
C006443
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY
SMS_ID
100000087716
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY
WIKIPEDIA
Albutoin
Created by admin on Sat Dec 16 16:54:41 GMT 2023 , Edited by admin on Sat Dec 16 16:54:41 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY