Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H13BrN2O2 |
Molecular Weight | 237.094 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(Br)(CC)C(=O)NC(N)=O
InChI
InChIKey=OPNPQXLQERQBBV-UHFFFAOYSA-N
InChI=1S/C7H13BrN2O2/c1-3-7(8,4-2)5(11)10-6(9)12/h3-4H2,1-2H3,(H3,9,10,11,12)
Carbromal is containing bromide mild hypnotic that has been used to mild insomnia treatment. Carbromal is one of a number of hypnotics containing bromide, which releases the bromide ion on hydrolysis in the body. It has no advantages over other hypnotics. Chronic administration can cause accumulation of bromide ions which have the same distribution as chloride ions but are not actively transported out of cells and are excreted in the urine with a half-life of 10-12 days. Bromism may result from chronic carbromal ingestion and with a plasma bromine concentration of 10-15 mM, the signs are acne, cerebral retardation, cerebellar dysfunction, hyperreflexia, extensor plantar responses, and gastro¬intestinal symptoms. The risk of bromism developing makes carbromal a more dangerous drug than most other hypnotics.
Approval Year
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
30 μM |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
CARBROMAL serum | Homo sapiens population: HEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
|
20 μM |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
BROMOETHYLBUTYRAMIDE serum | Homo sapiens population: HEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
Doses
Dose | Population | Adverse events |
---|---|---|
780 mg 1 times / day multiple, oral Recommended Dose: 780 mg, 1 times / day Route: oral Route: multiple Dose: 780 mg, 1 times / day Sources: |
unhealthy, 27-53 |
Disc. AE: Drug eruption... AEs leading to discontinuation/dose reduction: Drug eruption (6%) Sources: |
5850 mg 1 times / day multiple, oral Dose: 5850 mg, 1 times / day Route: oral Route: multiple Dose: 5850 mg, 1 times / day Sources: |
unhealthy, 54 |
Other AEs: Addiction... |
260 mg 1 times / day multiple, oral Recommended Dose: 260 mg, 1 times / day Route: oral Route: multiple Dose: 260 mg, 1 times / day Sources: |
unhealthy, 60-65 |
Other AEs: Drug eruption... |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Drug eruption | 6% Disc. AE |
780 mg 1 times / day multiple, oral Recommended Dose: 780 mg, 1 times / day Route: oral Route: multiple Dose: 780 mg, 1 times / day Sources: |
unhealthy, 27-53 |
Addiction | 1% | 5850 mg 1 times / day multiple, oral Dose: 5850 mg, 1 times / day Route: oral Route: multiple Dose: 5850 mg, 1 times / day Sources: |
unhealthy, 54 |
Drug eruption | 1% | 260 mg 1 times / day multiple, oral Recommended Dose: 260 mg, 1 times / day Route: oral Route: multiple Dose: 260 mg, 1 times / day Sources: |
unhealthy, 60-65 |
Name | Type | Language | ||
---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
WHO-ATC |
N05CM04
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
||
|
NCI_THESAURUS |
C29756
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
||
|
WHO-VATC |
QN05CM04
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
49191
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
0Y299JY9V3
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
53
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
504
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
2067
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | RxNorm | ||
|
SUB06617MIG
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
m1055
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | Merck Index | ||
|
100000084568
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
DTXSID8020252
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
77-65-6
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
6488
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
4100
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
201-046-6
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
CHEMBL1697828
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
C76936
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
C084812
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
DB13817
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY | |||
|
CARBROMAL
Created by
admin on Mon Mar 31 17:34:22 GMT 2025 , Edited by admin on Mon Mar 31 17:34:22 GMT 2025
|
PRIMARY |
ACTIVE MOIETY