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

Details

Stereochemistry RACEMIC
Molecular Formula C11H16N2O3
Molecular Weight 224.2563
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VINYLBITAL

SMILES

CCCC(C)C1(C=C)C(=O)NC(=O)NC1=O

InChI

InChIKey=KGKJZEKQJQQOTD-UHFFFAOYSA-N
InChI=1S/C11H16N2O3/c1-4-6-7(3)11(5-2)8(14)12-10(16)13-9(11)15/h5,7H,2,4,6H2,1,3H3,(H2,12,13,14,15,16)

HIDE SMILES / InChI

Molecular Formula C11H16N2O3
Molecular Weight 224.2563
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Vinylbital is a barbiturate derivative. It was introduced into therapy in 1963 and used as a sedative and in the treatment of insomnia.

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:47:49 GMT 2023
Edited
by admin
on Fri Dec 15 18:47:49 GMT 2023
Record UNII
3W58ITX06Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VINYLBITAL
INN   MART.   MI   WHO-DD  
INN  
Official Name English
BUTYLVINAL
Common Name English
vinylbital [INN]
Common Name English
2,4,6(1H,3H,5H)-PYRIMIDINETRIONE, 5-ETHENYL-5-(1-METHYLBUTYL)-
Systematic Name English
VINYMAL
Common Name English
VINYLBITAL [MI]
Common Name English
JD-96
Code English
JD96
Code English
BUTYVINYL
Common Name English
OPTANOX
Brand Name English
VINYLBITAL [MART.]
Common Name English
5-ETHENYL-5-(1-METHYLBUTYL)-2,4,6(1H,3H,5H)-PYRIMIDINETRIONE
Common Name English
Vinylbital [WHO-DD]
Common Name English
5-(1-METHYLBUTYL)-5-VINYLBARBITURIC ACID
Systematic Name English
SPEDA
Brand Name English
VINYLBITONE
Common Name English
BARBITURIC ACID, 5-(1-METHYLBUTYL)-5-VINYL-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29756
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
WHO-VATC QN05CA08
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
WHO-ATC N05CA08
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
219-395-8
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
PUBCHEM
72135
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
NCI_THESAURUS
C74377
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105552
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
INN
1153
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
RXCUI
19928
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY RxNorm
DRUG CENTRAL
2829
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
MERCK INDEX
m11460
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY Merck Index
DRUG BANK
DB13770
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
MESH
C013334
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
EVMPD
SUB00076MIG
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
FDA UNII
3W58ITX06Q
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
WIKIPEDIA
VINYLBITAL
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
CAS
2430-49-1
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
SMS_ID
100000079137
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
EPA CompTox
DTXSID50862938
Created by admin on Fri Dec 15 18:47:49 GMT 2023 , Edited by admin on Fri Dec 15 18:47:49 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY