Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H14N2O3 |
| Molecular Weight | 210.2298 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C1(CC=C)C(=O)NC(=O)NC1=O
InChI
InChIKey=UORJNBVJVRLXMQ-UHFFFAOYSA-N
InChI=1S/C10H14N2O3/c1-4-5-10(6(2)3)7(13)11-9(15)12-8(10)14/h4,6H,1,5H2,2-3H3,(H2,11,12,13,14,15)
| Molecular Formula | C10H14N2O3 |
| Molecular Weight | 210.2298 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: https://www.drugs.com/mmx/aprobarbital.html
Sources: https://www.drugs.com/mmx/aprobarbital.html
Aprobarbital is a barbiturate derivative. Aprobarbital have been used for the short-term treatment of insomnia and for routine sedation to relieve anxiety, tension, and apprehension however, barbiturates generally have been replaced by benzodiazepines.
CNS Activity
Originator
Sources: http://www.trademarkia.com/alurate-71245642.html | https://en.wikipedia.org/wiki/Aprobarbital
Curator's Comment: On Saturday, March 12, 1927, a U.S. federal trademark registration was filed for ALURATE (trade name for Aprobarbital) by Hoffmann-La Roche Inc.. According to Wikipedia Aprobarbital was invented in the 1920s by Ernst Preiswerk (No additional reference available). # Hoffmann-La Roche Inc.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2093872 Sources: https://www.drugbank.ca/drugs/DB01352 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | ALURATE Approved UseAprobarbital have been used for the short-term treatment of insomnia and for routine sedation to relieve anxiety, tension, and apprehension however, barbiturates generally have been replaced by benzodiazepines. Launch Date1927 |
|||
| Primary | ALURATE Approved UseAprobarbital have been used for the short-term treatment of insomnia and for routine sedation to relieve anxiety, tension, and apprehension however, barbiturates generally have been replaced by benzodiazepines. Launch Date1927 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Occurrence and fate of barbiturates in the aquatic environment. | 2006-12-01 |
|
| The history of barbiturates a century after their clinical introduction. | 2005-12 |
|
| Determinations of zidovudine/didanosine/nevirapine and zidovudine/didanosine/ritonavir in human serum by micellar electrokinetic chromatography. | 2002-11-07 |
|
| Determination of lamivudine/stavudine/efavirenz in human serum using liquid chromatography/electrospray tandem mass spectrometry with ionization polarity switch. | 2002-09 |
|
| Determination of zidovudine/lamivudine/nevirapine in human plasma using ion-pair HPLC. | 2002-06-01 |
|
| Permanent impairment of renal function after methicillin nephropathy. | 1971-11-13 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.drugs.com/mmx/aprobarbital.html
Usual adult dose
Hypnotic: Oral, 40 to 160 mg at bedtime.
Sedative: Daytime—Oral, 40 mg three times a day.
Route of Administration:
Oral
| Substance Class |
Chemical
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Q0YKG9L6RF
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NCI_THESAURUS |
C67084
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WHO-ATC |
N05CA05
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DEA NO. |
2100
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WHO-VATC |
QN05CA05
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1161
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6464
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Q0YKG9L6RF
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120769
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DTXSID8022616
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CHEMBL7863
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200-997-4
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2791
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C006470
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3290
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APROBARBITAL
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232
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77-02-1
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100000087182
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SUB05543MIG
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m2015
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C76525
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17381
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DB01352
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ACTIVE MOIETY |