EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C6H10O6 |
| Net Charge | 0 |
| Average Mass | 178.140 |
| Monoisotopic Mass | 178.04774 |
| SMILES | [H][C@]1([C@@H](O)CO)OC(=O)[C@@H](O)[C@H]1O |
| InChI | InChI=1S/C6H10O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h2-5,7-10H,1H2/t2-,3+,4-,5+/m0/s1 |
| InChIKey | SXZYCXMUPBBULW-SKNVOMKLSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Homo sapiens (ncbitaxon:9606) | - | DOI (10.1038/nbt.2488) | |
| Mus musculus (ncbitaxon:10090) | - | PubMed (19425150) | Source: BioModels - MODEL1507180067 |
| Roles Classification |
|---|
| Biological Roles: | human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| L-gulono-1,4-lactone (CHEBI:17587) has functional parent L-gulonic acid (CHEBI:16154) |
| L-gulono-1,4-lactone (CHEBI:17587) has role human metabolite (CHEBI:77746) |
| L-gulono-1,4-lactone (CHEBI:17587) has role mouse metabolite (CHEBI:75771) |
| L-gulono-1,4-lactone (CHEBI:17587) is a gulonolactone (CHEBI:37433) |
| IUPAC Name |
|---|
| (3S,4R,5R)-5-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxydihydrofuran-2(3H)-one |
| Synonyms | Source |
|---|---|
| L-Gulono-1,4-lactone | KEGG COMPOUND |
| L-Gulono-gamma-lactone | KEGG COMPOUND |
| gamma-Gulonolactone | KEGG COMPOUND |
| L-Gulonic acid gamma-lactone | KEGG COMPOUND |
| L-Gulonolactone | KEGG COMPOUND |
| UniProt Name | Source |
|---|---|
| L-gulono-1,4-lactone | UniProt |
| Manual Xrefs | Databases |
|---|---|
| C01040 | KEGG COMPOUND |
| HMDB0003466 | HMDB |
| Registry Numbers | Sources |
|---|---|
| Reaxys:83002 | Reaxys |
| CAS:1128-23-0 | KEGG COMPOUND |
| Citations |
|---|