EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C5H7O4 |
| Net Charge | -1 |
| Average Mass | 131.107 |
| Monoisotopic Mass | 131.03498 |
| SMILES | CC(=O)C(C)(O)C(=O)[O-] |
| InChI | InChI=1S/C5H8O4/c1-3(6)5(2,9)4(7)8/h9H,1-2H3,(H,7,8)/p-1 |
| InChIKey | NMDWGEGFJUBKLB-UHFFFAOYSA-M |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Saccharomyces cerevisiae (ncbitaxon:4932) | - | PubMed (24678285) | Source: yeast.sf.net |
| Roles Classification |
|---|
| Biological Role: | Saccharomyces cerevisiae metabolite Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| 2-acetyllactate (CHEBI:57774) has role Saccharomyces cerevisiae metabolite (CHEBI:75772) |
| 2-acetyllactate (CHEBI:57774) is a 2-oxo monocarboxylic acid anion (CHEBI:35179) |
| 2-acetyllactate (CHEBI:57774) is a hydroxy monocarboxylic acid anion (CHEBI:36059) |
| 2-acetyllactate (CHEBI:57774) is conjugate base of 2-acetyllactic acid (CHEBI:16444) |
| Incoming Relation(s) |
| 2-acetyllactic acid (CHEBI:16444) is conjugate acid of 2-acetyllactate (CHEBI:57774) |
| IUPAC Name |
|---|
| 2-hydroxy-2-methyl-3-oxobutanoate |
| Synonyms | Source |
|---|---|
| 2-acetyllactate anion | ChEBI |
| 2-acetyllactate(1−) | ChEBI |
| UniProt Name | Source |
|---|---|
| 2-acetolactate | UniProt |
| Registry Numbers | Sources |
|---|---|
| Beilstein:7089436 | Beilstein |