Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C7H8NO3.Na |
| Molecular Weight | 177.1331 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].C[C-]1OC(=O)N(CC=C)C1=O
InChI
InChIKey=QXGBKVKAWTZKOL-UHFFFAOYSA-N
InChI=1S/C7H8NO3.Na/c1-3-4-8-6(9)5(2)11-7(8)10;/h3H,1,4H2,2H3;/q-1;+1
| Molecular Formula | C7H9NO3 |
| Molecular Weight | 155.1513 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
| Molecular Formula | Na |
| Molecular Weight | 22.98976928 |
| Charge | 1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Allomethadione is an anticonvulsant. It was used for the treatment of epilepsy. Allomethadione appears to have the advantage over tridione (another anticonvulsant) in not producing ataxia or gastric irritation. Photophobia is common in patients taking tridione but allomethadione did not produce photophobia. The drug causes renal damage. The compound has been marketed in Europe.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:35:32 GMT 2025
by
admin
on
Mon Mar 31 23:35:32 GMT 2025
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| Record UNII |
X358SB601N
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| Record Status |
Validated (UNII)
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| Record Version |
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91810501
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6058-46-4
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DTXSID50412194
Created by
admin on Mon Mar 31 23:35:32 GMT 2025 , Edited by admin on Mon Mar 31 23:35:32 GMT 2025
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X358SB601N
Created by
admin on Mon Mar 31 23:35:32 GMT 2025 , Edited by admin on Mon Mar 31 23:35:32 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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