EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C4H6NO4 |
| Net Charge | -1 |
| Average Mass | 132.095 |
| Monoisotopic Mass | 132.03023 |
| SMILES | [NH3+][C@@H](CC(=O)[O-])C(=O)[O-] |
| InChI | InChI=1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/p-1/t2-/m0/s1 |
| InChIKey | CKLJMWTZIZZHCS-REOHCLBHSA-M |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Homo sapiens (ncbitaxon:9606) | - | DOI (10.1038/nbt.2488) | |
| Saccharomyces cerevisiae (ncbitaxon:4932) | - | PubMed (24678285) | Source: yeast.sf.net |
| Roles Classification |
|---|
| Biological Roles: | human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). fundamental metabolite Any metabolite produced by all living cells. fundamental metabolite Any metabolite produced by all living cells. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| L-aspartate(1−) (CHEBI:29991) has role fundamental metabolite (CHEBI:78675) |
| L-aspartate(1−) (CHEBI:29991) has role human metabolite (CHEBI:77746) |
| L-aspartate(1−) (CHEBI:29991) is a L-α-amino acid zwitterion (CHEBI:59869) |
| L-aspartate(1−) (CHEBI:29991) is a aspartate(1−) (CHEBI:35391) |
| L-aspartate(1−) (CHEBI:29991) is a polar amino acid zwitterion (CHEBI:62031) |
| L-aspartate(1−) (CHEBI:29991) is conjugate acid of L-aspartate(2−) (CHEBI:29993) |
| L-aspartate(1−) (CHEBI:29991) is conjugate base of L-aspartic acid (CHEBI:17053) |
| L-aspartate(1−) (CHEBI:29991) is enantiomer of D-aspartate(1−) (CHEBI:29990) |
| Incoming Relation(s) |
| L-aspartate 4-semialdehyde (CHEBI:13086) has functional parent L-aspartate(1−) (CHEBI:29991) |
| L-aspartic acid (CHEBI:17053) is conjugate acid of L-aspartate(1−) (CHEBI:29991) |
| L-aspartate(2−) (CHEBI:29993) is conjugate base of L-aspartate(1−) (CHEBI:29991) |
| D-aspartate(1−) (CHEBI:29990) is enantiomer of L-aspartate(1−) (CHEBI:29991) |
| L-aspartate residue (CHEBI:29961) is substituent group from L-aspartate(1−) (CHEBI:29991) |
| IUPAC Name |
|---|
| hydrogen L-aspartate |
| Synonyms | Source |
|---|---|
| (2S)-2-ammoniobutanedioate | IUPAC |
| (2S)-2-ammoniosuccinate | ChEBI |
| L-aspartate | ChEBI |
| L-aspartate(1−) | JCBN |
| L-aspartic acid monoanion | JCBN |
| UniProt Name | Source |
|---|---|
| L-aspartate | UniProt |
| Registry Numbers | Sources |
|---|---|
| Reaxys:15801578 | Reaxys |
| Gmelin:327374 | Gmelin |