Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H14N2O4 |
| Molecular Weight | 226.2292 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(O)CC1(CC=C)C(=O)NC(=O)NC1=O
InChI
InChIKey=VNLMRPAWAMPLNZ-UHFFFAOYSA-N
InChI=1S/C10H14N2O4/c1-3-4-10(5-6(2)13)7(14)11-9(16)12-8(10)15/h3,6,13H,1,4-5H2,2H3,(H2,11,12,14,15,16)
Proxibarbal is a non-sedative barbiturate with a specific anti-serotonin and anti-histamine effect, due to enzyme induction of serotoninase and histaminase. Its lack of unpleasant side-effects. Proxibarbal exists in ring-chain tautomeric equilibrium with the two diastereomers of valofan. Proxibarbal is metabolized to a five-membered lactone. Its only barbituric property is its ability to induce enzymes that destroy a surplus of neurohormones and rid people of their neurovegetative sufferings, including migraine and other types of vascular headache. Side effects are: dizziness, drowsiness, dyspepsia, allergic reactions. Proxibarbal enhances the effects of other depriving agents, including alcohol.
Approval Year
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29756
Created by
admin on Wed Apr 02 09:56:02 GMT 2025 , Edited by admin on Wed Apr 02 09:56:02 GMT 2025
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WHO-VATC |
QN05CA22
Created by
admin on Wed Apr 02 09:56:02 GMT 2025 , Edited by admin on Wed Apr 02 09:56:02 GMT 2025
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WHO-ATC |
N05CA22
Created by
admin on Wed Apr 02 09:56:02 GMT 2025 , Edited by admin on Wed Apr 02 09:56:02 GMT 2025
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| Code System | Code | Type | Description | ||
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3734
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m9283
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DTXSID20862980
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F97OMS297F
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CHEMBL2105233
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2537-29-3
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219-803-4
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17336
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2322
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83885
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100000080858
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DB13253
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SUB10147MIG
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C084552
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admin on Wed Apr 02 09:56:02 GMT 2025 , Edited by admin on Wed Apr 02 09:56:02 GMT 2025
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C74375
Created by
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42013-34-3
Created by
admin on Wed Apr 02 09:56:02 GMT 2025 , Edited by admin on Wed Apr 02 09:56:02 GMT 2025
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SUPERSEDED | |||
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Proxibarbital
Created by
admin on Wed Apr 02 09:56:02 GMT 2025 , Edited by admin on Wed Apr 02 09:56:02 GMT 2025
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PRIMARY |
ACTIVE MOIETY