EMBL-EBI | Chemical Biology | ChEBI
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| ChEBI ID | CHEBI:134870 |
| ChEBI Name | toloxatone |
| Stars | |
| Definition | A racemate consisting of equimolar amounts of (R)- and (S)-toloxatone. It is a reversible monoamine oxidase A inhibitor and antidepressant. |
| Last Modified | 2 October 2020 |
| Formula | C11H13NO3 |
| Net Charge | 0 |
| Average Mass | 207.229 |
| Monoisotopic Mass | 207.08954 |
| Wikipedia |
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| Roles Classification |
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| Biological Role: | EC 1.4.3.4 (monoamine oxidase) inhibitor An EC 1.4.3.* (oxidoreductase acting on donor CH-NH2 group, oxygen as acceptor) inhibitor that interferes with the action of monoamine oxidase (EC 1.4.3.4). |
| Application: | antidepressant Antidepressants are mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| toloxatone (CHEBI:134870) has part (R)-toloxatone (CHEBI:156573) |
| toloxatone (CHEBI:134870) has part (S)-toloxatone (CHEBI:156574) |
| toloxatone (CHEBI:134870) has role antidepressant (CHEBI:35469) |
| toloxatone (CHEBI:134870) has role EC 1.4.3.4 (monoamine oxidase) inhibitor (CHEBI:38623) |
| toloxatone (CHEBI:134870) is a racemate (CHEBI:60911) |
| IUPAC Name |
|---|
| rac-5-(hydroxymethyl)-3-(3-methylphenyl)-1,3-oxazolidin-2-one |
| INNs | Source |
|---|---|
| toloxatone | WHO MedNet |
| toloxatone | WHO MedNet |
| toloxatona | WHO MedNet |
| toloxatonum | WHO MedNet |
| Synonyms | Source |
|---|---|
| rac-toloxatone | ChEBI |
| racemic toloxatone | ChEBI |
| (RS)-toloxatone | ChEBI |
| (5RS)-5-(hydroxymethyl)-3-(3-methylphenyl)-1,3-oxazolidin-2-one | ChEBI |
| rac-5-(hydroxymethyl)-3-(3-methylphenyl)-2-oxazolidinone | ChEBI |
| rac-5-hydroxymethyl-3-(m-tolyl)-2-oxazolidinone | ChEBI |
| Brand Names | Source |
|---|---|
| Humoryl | KEGG DRUG |
| Perenum | ChemIDplus |
| Manual Xrefs | Databases |
|---|---|
| 2702 | DrugCentral |
| DB09245 | DrugBank |
| D02559 | KEGG DRUG |
| Toloxatone | Wikipedia |
| US4699782 | Patent |
| Registry Numbers | Sources |
|---|---|
| Reaxys:527506 | Reaxys |
| CAS:29218-27-7 | ChemIDplus |
| Citations |
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