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Details

Stereochemistry RACEMIC
Molecular Formula C12H20N2O3
Molecular Weight 240.2988
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIBERAL

SMILES

CCC1(C(C)CC(C)C)C(=O)NC(=O)NC1=O

InChI

InChIKey=KXHLANWWTKSOMW-UHFFFAOYSA-N
InChI=1S/C12H20N2O3/c1-5-12(8(4)6-7(2)3)9(15)13-11(17)14-10(12)16/h7-8H,5-6H2,1-4H3,(H2,13,14,15,16,17)

HIDE SMILES / InChI

Molecular Formula C12H20N2O3
Molecular Weight 240.2988
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
The effects of barbiturates on the metabolism of phosphatidic acid and phosphatidylinositol in rat brain synaptosomes.
1979 Jan 15
Characterization of barbiturate-stimulated chloride efflux from rat brain synaptoneurosomes.
1985 Nov
Regulation of [35S]t-butylbicyclophosphorothionate binding sites in rat brain by GABA, pyrethroid and barbiturate.
1985 Sep 24
Facilitation of recurrent inhibition in rat hippocampus by barbiturate and related nonbarbiturate depressant drugs.
1986 Aug
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:04:53 GMT 2023
Edited
by admin
on Sat Dec 16 10:04:53 GMT 2023
Record UNII
31E1HC8I46
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIBERAL
Common Name English
5-ETHYL-5-(1,3-DIMETHYLBUTYL) BARBITURIC ACID
Systematic Name English
DMBEB
Common Name English
2,4,6(1H,3H,5H)-PYRIMIDINETRIONE, 5-(1,3-DIMETHYLBUTYL)-5-ETHYL-
Systematic Name English
PENTOBARBITAL SODIUM IMPURITY F [EP IMPURITY]
Common Name English
5-ETHYL-5-(1,3-DIMETHYLBUTYL)BARBITURIC ACID
Systematic Name English
DMBB
Common Name English
NSC-31256
Code English
(±)-5-(1,3-DIMETHYLBUTYL)-5-ETHYLBARBITURIC ACID
Systematic Name English
5-(1,3-DIMETHYLBUTYL)-5-ETHYLBARBITURIC ACID
Systematic Name English
PENTOBARBITAL IMPURITY F [EP IMPURITY]
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID301031188
Created by admin on Sat Dec 16 10:04:54 GMT 2023 , Edited by admin on Sat Dec 16 10:04:54 GMT 2023
PRIMARY
FDA UNII
31E1HC8I46
Created by admin on Sat Dec 16 10:04:54 GMT 2023 , Edited by admin on Sat Dec 16 10:04:54 GMT 2023
PRIMARY
NSC
31256
Created by admin on Sat Dec 16 10:04:54 GMT 2023 , Edited by admin on Sat Dec 16 10:04:54 GMT 2023
PRIMARY
PUBCHEM
18079
Created by admin on Sat Dec 16 10:04:54 GMT 2023 , Edited by admin on Sat Dec 16 10:04:54 GMT 2023
PRIMARY
CAS
2964-06-9
Created by admin on Sat Dec 16 10:04:54 GMT 2023 , Edited by admin on Sat Dec 16 10:04:54 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP