Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H15N2O3.Na |
| Molecular Weight | 234.2275 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].CCC(C)C1(CC)C(=O)NC(=O)[N-]C1=O
InChI
InChIKey=QORQZMBCPRBCAB-UHFFFAOYSA-M
InChI=1S/C10H16N2O3.Na/c1-4-6(3)10(5-2)7(13)11-9(15)12-8(10)14;/h6H,4-5H2,1-3H3,(H2,11,12,13,14,15);/q;+1/p-1
Barbiturates are non-selective depressants of the central nervous system. Butabarbital is one of them, which is used under brand name butisol sodium as a sedative or hypnotic. Like other barbiturates, butabarbital is capable of producing all levels of CNS mood alteration from excitation to mild sedation, to hypnosis, and deep coma. The mechanism of action by which barbiturates exert their effect is not yet completely understood, but is assumed, that butabarbital binds at a distinct binding site associated with a Cl- ionopore at the GABAA receptor, increasing the duration of time for which the Cl- ionopore is open. The post-synaptic inhibitory effect of GABA in the thalamus is, therefore, prolonged.
CNS Activity
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2093872 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11264449 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | BUTISOL SODIUM Approved UseBUTISOL SODIUM (butabarbital sodium tablets, USP and butabarbital sodium oral solution, USP) is indicated for use as a sedative or hypnotic. Since barbiturates appear to lose their effectiveness for sleep induction and sleep maintenance after 2 weeks, use of BUTISOL SODIUM in treating insomnia should be limited to this time. Launch Date1939 |
Doses
| Dose | Population | Adverse events |
|---|---|---|
15 mg 4 times / day multiple, oral Recommended Dose: 15 mg, 4 times / day Route: oral Route: multiple Dose: 15 mg, 4 times / day Sources: |
unhealthy, 36 |
Disc. AE: Drowsiness... AEs leading to discontinuation/dose reduction: Drowsiness (1 patient) Sources: |
30 mg 4 times / day multiple, oral Recommended Dose: 30 mg, 4 times / day Route: oral Route: multiple Dose: 30 mg, 4 times / day Sources: |
unhealthy, adult |
Other AEs: Sedation... |
30 mg 4 times / day multiple, oral Recommended Dose: 30 mg, 4 times / day Route: oral Route: multiple Dose: 30 mg, 4 times / day Sources: |
unhealthy, adult |
Other AEs: Sedation... |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Drowsiness | 1 patient Disc. AE |
15 mg 4 times / day multiple, oral Recommended Dose: 15 mg, 4 times / day Route: oral Route: multiple Dose: 15 mg, 4 times / day Sources: |
unhealthy, 36 |
| Sedation | 10 patients | 30 mg 4 times / day multiple, oral Recommended Dose: 30 mg, 4 times / day Route: oral Route: multiple Dose: 30 mg, 4 times / day Sources: |
unhealthy, adult |
| Sedation | 14 patients | 30 mg 4 times / day multiple, oral Recommended Dose: 30 mg, 4 times / day Route: oral Route: multiple Dose: 30 mg, 4 times / day Sources: |
unhealthy, adult |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
OverviewOther
| Other Inhibitor | Other Substrate | Other Inducer |
|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| yes |
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Sources: https://pubmed.ncbi.nlm.nih.gov/30443785/ Page: 11.0 |
yes | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/30443785/ Page: 11.0 |
yes |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Adverse drug effects in hospitalized elderly: data from the healthcare cost and utilization project. | 2010 |
|
| Management of acute diarrhoea in primary care in Bahrain: self-reported practices of doctors. | 2007-06 |
|
| Treatment with the xanthine oxidase inhibitor, allopurinol, improves nerve and vascular function in diabetic rats. | 2007-04-30 |
|
| The history of barbiturates a century after their clinical introduction. | 2005-12 |
|
| Comparative abuse liability and pharmacological effects of meprobamate, triazolam, and butabarbital. | 2003-06 |
Sample Use Guides
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| Classification Tree | Code System | Code | ||
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DEA NO. |
2100
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NCI_THESAURUS |
C67084
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143-81-7
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9WTD50I918
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C65275
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11778
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CHEMBL449
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DBSALT000312
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m2779
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100000085038
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SUB04343MIG
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23690439
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DTXSID70874119
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91109
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205-611-8
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ACTIVE MOIETY
SUBSTANCE RECORD