EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C6H10NO4 |
| Net Charge | -1 |
| Average Mass | 160.149 |
| Monoisotopic Mass | 160.06153 |
| SMILES | [NH3+][C@@H](CCCC(=O)[O-])C(=O)[O-] |
| InChI | InChI=1S/C6H11NO4/c7-4(6(10)11)2-1-3-5(8)9/h4H,1-3,7H2,(H,8,9)(H,10,11)/p-1/t4-/m0/s1 |
| InChIKey | OYIFNHCXNCRBQI-BYPYZUCNSA-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). Saccharomyces cerevisiae metabolite Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| L-2-aminoadipate(1−) (CHEBI:58672) has role Saccharomyces cerevisiae metabolite (CHEBI:75772) |
| L-2-aminoadipate(1−) (CHEBI:58672) has role human metabolite (CHEBI:77746) |
| L-2-aminoadipate(1−) (CHEBI:58672) is a α-amino-acid anion (CHEBI:33558) |
| L-2-aminoadipate(1−) (CHEBI:58672) is conjugate acid of L-2-aminoadipate(2−) (CHEBI:17082) |
| L-2-aminoadipate(1−) (CHEBI:58672) is conjugate base of L-2-aminoadipic acid (CHEBI:37023) |
| Incoming Relation(s) |
| L-2-aminoadipic acid (CHEBI:37023) is conjugate acid of L-2-aminoadipate(1−) (CHEBI:58672) |
| L-2-aminoadipate(2−) (CHEBI:17082) is conjugate base of L-2-aminoadipate(1−) (CHEBI:58672) |
| L-2-aminoadipate(1−) residue (CHEBI:235404) is substituent group from L-2-aminoadipate(1−) (CHEBI:58672) |
| IUPAC Name |
|---|
| (2S)-2-azaniumylhexanedioate |
| UniProt Name | Source |
|---|---|
| L-2-aminoadipate | UniProt |