EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C10H8O |
| Net Charge | 0 |
| Average Mass | 144.173 |
| Monoisotopic Mass | 144.05751 |
| SMILES | C1=C[C@H]2O[C@H]2c2ccccc21 |
| InChI | InChI=1S/C10H8O/c1-2-4-8-7(3-1)5-6-9-10(8)11-9/h1-6,9-10H/t9-,10+/m1/s1 |
| InChIKey | XQIJIALOJPIKGX-ZJUUUORDSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Mus musculus (ncbitaxon:10090) | - | PubMed (19425150) | Source: BioModels - MODEL1507180067 |
| Roles Classification |
|---|
| Biological Role: | mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| (1S,2R)-naphthalene 1,2-oxide (CHEBI:34001) has role mouse metabolite (CHEBI:75771) |
| (1S,2R)-naphthalene 1,2-oxide (CHEBI:34001) is a naphthalene 1,2-oxide (CHEBI:52431) |
| (1S,2R)-naphthalene 1,2-oxide (CHEBI:34001) is enantiomer of (1R,2S)-naphthalene 1,2-oxide (CHEBI:33998) |
| Incoming Relation(s) |
| (1R,2S)-naphthalene 1,2-oxide (CHEBI:33998) is enantiomer of (1S,2R)-naphthalene 1,2-oxide (CHEBI:34001) |
| IUPAC Name |
|---|
| (1aR,7bS)-1a,7b-dihydronaphtho[1,2-b]oxirene |
| Synonyms | Source |
|---|---|
| (1S,2R)-naphthalene 1,2-oxide | KEGG COMPOUND |
| (1S,2R)-naphthalene epoxide | KEGG COMPOUND |
| (1aR,7bS)-1aH,7bH-naphtho[1,2-b]oxirene | ChEBI |
| (1S,2R)-1,2-dihydro-1,2-epoxynaphthalene | ChEBI |
| (1S,2R)-1,2-epoxy-1,2-dihydronaphthalene | ChEBI |
| (−)-(1S,2R)-naphthalene 1,2-oxide | ChEBI |
| Manual Xrefs | Databases |
|---|---|
| C14787 | KEGG COMPOUND |
| HMDB0060301 | HMDB |
| Registry Numbers | Sources |
|---|---|
| CAS:24825-00-1 | ChEBI |
| Citations |
|---|