EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C4H6O4 |
| Net Charge | 0 |
| Average Mass | 118.088 |
| Monoisotopic Mass | 118.02661 |
| SMILES | O=C1OC[C@H](O)[C@H]1O |
| InChI | InChI=1S/C4H6O4/c5-2-1-8-4(7)3(2)6/h2-3,5-6H,1H2/t2-,3+/m0/s1 |
| InChIKey | SGMJBNSHAZVGMC-STHAYSLISA-N |
| Roles Classification |
|---|
| Biological Role: | metabolite Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| L-threonolactone (CHEBI:71176) has role metabolite (CHEBI:25212) |
| L-threonolactone (CHEBI:71176) is a butan-4-olide (CHEBI:22950) |
| L-threonolactone (CHEBI:71176) is a diol (CHEBI:23824) |
| L-threonolactone (CHEBI:71176) is enantiomer of D-threonolactone (CHEBI:87770) |
| Incoming Relation(s) |
| D-threonolactone (CHEBI:87770) is enantiomer of L-threonolactone (CHEBI:71176) |
| IUPAC Name |
|---|
| (3R,4S)-3,4-dihydroxydihydrofuran-2(3H)-one |
| Synonyms | Source |
|---|---|
| Threonic acid-1,4-lactone | HMDB |
| L-threonic acid-1,4-lactone | ChEBI |
| Manual Xrefs | Databases |
|---|---|
| HMDB0000940 | HMDB |
| Registry Numbers | Sources |
|---|---|
| Reaxys:81074 | Reaxys |
| CAS:21730-93-8 | HMDB |
| Citations |
|---|