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Details

Stereochemistry ACHIRAL
Molecular Formula C10H11BrN2O3
Molecular Weight 287.11
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BRALLOBARBITAL

SMILES

BrC(=C)CC1(CC=C)C(=O)NC(=O)NC1=O

InChI

InChIKey=DYODAJAEQDVYFX-UHFFFAOYSA-N
InChI=1S/C10H11BrN2O3/c1-3-4-10(5-6(2)11)7(14)12-9(16)13-8(10)15/h3H,1-2,4-5H2,(H2,12,13,14,15,16)

HIDE SMILES / InChI

Molecular Formula C10H11BrN2O3
Molecular Weight 287.11
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Brallobarbital possessed the sedative and hypnotic properties and was a component of Vesparax that was used to treat sleep disorders. However, was revealed that brallobarbital was responsible for the problems in Vesparax intoxication.

Approval Year

PubMed

PubMed

TitleDatePubMed
Rapid toxicological screening of barbiturates in plasma by wide-bore capillary gas chromatography and nitrogen-phosphorus detection.
1993-03-01
[Excretion ratios of brallobarbital in man].
1969-04
[Isolation and identification of brallobarbital metabolites].
1969-03
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:26:42 GMT 2025
Edited
by admin
on Mon Mar 31 18:26:42 GMT 2025
Record UNII
D0N7A2M3MU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BRALLOBARBITAL
INN   MART.   MI   WHO-DD  
INN  
Official Name English
T2G1S
Preferred Name English
(±)-BRALLOBARBITAL
Common Name English
BRALLOBARBITAL, (±)-
Common Name English
BRALLOBARBITAL [MI]
Common Name English
BRALLOBARBITAL [MART.]
Common Name English
5-ALLYL-5-(2-BROMOALLYL)BARBITURIC ACID
Systematic Name English
brallobarbital [INN]
Common Name English
Brallobarbital [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C67084
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
Code System Code Type Description
MESH
C012790
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-225-0
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
NCI_THESAURUS
C74380
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
CAS
561-86-4
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
DRUG CENTRAL
393
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
ChEMBL
CHEMBL2106093
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
EVMPD
SUB05880MIG
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
PUBCHEM
68416
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
SMS_ID
100000088640
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
INN
8
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
MERCK INDEX
m2636
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY Merck Index
FDA UNII
D0N7A2M3MU
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
WIKIPEDIA
Brallobarbital
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
ChEMBL
CHEMBL2109283
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
EPA CompTox
DTXSID60204648
Created by admin on Mon Mar 31 18:26:42 GMT 2025 , Edited by admin on Mon Mar 31 18:26:42 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY