EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C5H10NO2 |
| Net Charge | -1 |
| Average Mass | 116.140 |
| Monoisotopic Mass | 116.07170 |
| SMILES | CC(C)[C@H](N)C(=O)[O-] |
| InChI | InChI=1S/C5H11NO2/c1-3(2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H,7,8)/p-1/t4-/m0/s1 |
| InChIKey | KZSNJWFQEVHDMF-BYPYZUCNSA-M |
| Roles Classification |
|---|
| Biological Role: | plant metabolite Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| L-valinate (CHEBI:32851) has role plant metabolite (CHEBI:76924) |
| L-valinate (CHEBI:32851) is a L-α-amino acid anion (CHEBI:59814) |
| L-valinate (CHEBI:32851) is a valinate (CHEBI:32859) |
| L-valinate (CHEBI:32851) is conjugate base of L-valine (CHEBI:16414) |
| L-valinate (CHEBI:32851) is enantiomer of D-valinate (CHEBI:32855) |
| Incoming Relation(s) |
| L-valine (CHEBI:16414) is conjugate acid of L-valinate (CHEBI:32851) |
| D-valinate (CHEBI:32855) is enantiomer of L-valinate (CHEBI:32851) |
| IUPAC Name |
|---|
| L-valinate |
| Synonyms | Source |
|---|---|
| (2S)-2-amino-3-methylbutanoate | IUPAC |
| L-valine anion | JCBN |
| Registry Numbers | Sources |
|---|---|
| Gmelin:325409 | Gmelin |
| Beilstein:3933569 | Beilstein |