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| ChEBI ID | CHEBI:31304 |
| ChEBI Name | bromisoval |
| Stars | |
| Definition | A racemate comprising equimolar amounts of (R)- and (S)-bromisoval. It was previously used for its hypnotic and sedative properties but the use of bromides is now deprecated due to the possibility of the toxic accumulation of bromine in the body. |
| Last Modified | 22 February 2017 |
| Formula | C6H11BrN2O2 |
| Net Charge | 0 |
| Average Mass | 223.068 |
| Monoisotopic Mass | 222.00039 |
| Wikipedia |
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| Roles Classification |
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| Application: | sedative A central nervous system depressant used to induce drowsiness or sleep or to reduce psychological excitement or anxiety. |
| ChEBI Ontology |
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| Outgoing Relation(s) |
| bromisoval (CHEBI:31304) has part (R)-bromisoval (CHEBI:77044) |
| bromisoval (CHEBI:31304) has part (S)-bromisoval (CHEBI:77045) |
| bromisoval (CHEBI:31304) has role sedative (CHEBI:35717) |
| bromisoval (CHEBI:31304) is a racemate (CHEBI:60911) |
| IUPAC Name |
|---|
| rac-2-bromo-N-carbamoyl-3-methylbutanamide |
| INNs | Source |
|---|---|
| bromisoval | WHO MedNet |
| bromisoval | WHO MedNet |
| bromisovalum | WHO MedNet |
| bromisoval | WHO MedNet |
| Synonyms | Source |
|---|---|
| Bromisovalum | KEGG COMPOUND |
| Bromovalerylurea | KEGG COMPOUND |
| (α-bromoisovaleroyl)urea | NIST Chemistry WebBook |
| (α-bromoisovaleryl)urea | NIST Chemistry WebBook |
| α-bromisovalerylurea | NIST Chemistry WebBook |
| α-bromoisovaleric acid ureide | NIST Chemistry WebBook |
| Brand Names | Source |
|---|---|
| Abroval | NIST Chemistry WebBook |
| Alluval | NIST Chemistry WebBook |
| Bromaral | NIST Chemistry WebBook |
| Alural | NIST Chemistry WebBook |
| Manual Xrefs | Databases |
|---|---|
| C12829 | KEGG COMPOUND |
| US914518 | Patent |
| D01391 | KEGG DRUG |
| Bromisoval | Wikipedia |
| Registry Numbers | Sources |
|---|---|
| Reaxys:1724352 | Reaxys |
| CAS:496-67-3 | KEGG COMPOUND |
| CAS:496-67-3 | NIST Chemistry WebBook |
| Citations |
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