EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C6H10N3O2 |
| Net Charge | +1 |
| Average Mass | 156.165 |
| Monoisotopic Mass | 156.07675 |
| SMILES | [NH3+][C@H](Cc1cnc[nH+]1)C(=O)[O-] |
| InChI | InChI=1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/p+1/t5-/m1/s1 |
| InChIKey | HNDVDQJCIGZPNO-RXMQYKEDSA-O |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Saccharomyces cerevisiae (ncbitaxon:4932) | - | PubMed (15744050) |
| 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) |
| D-histidinium(1+) (CHEBI:32526) has role Saccharomyces cerevisiae metabolite (CHEBI:75772) |
| D-histidinium(1+) (CHEBI:32526) is a histidinium(1+) (CHEBI:32531) |
| D-histidinium(1+) (CHEBI:32526) is conjugate acid of D-histidine (CHEBI:27947) |
| D-histidinium(1+) (CHEBI:32526) is conjugate base of D-histidinium(2+) (CHEBI:32527) |
| D-histidinium(1+) (CHEBI:32526) is enantiomer of L-histidinium(1+) (CHEBI:32513) |
| Incoming Relation(s) |
| D-histidinium(2+) (CHEBI:32527) is conjugate acid of D-histidinium(1+) (CHEBI:32526) |
| D-histidine (CHEBI:27947) is conjugate base of D-histidinium(1+) (CHEBI:32526) |
| L-histidinium(1+) (CHEBI:32513) is enantiomer of D-histidinium(1+) (CHEBI:32526) |
| D-histidinium residue (CHEBI:29981) is substituent group from D-histidinium(1+) (CHEBI:32526) |
| IUPAC Name |
|---|
| D-histidinium |
| Synonyms | Source |
|---|---|
| (2R)-2-ammonio-3-(1H-imidazol-3-ium-4-yl)propanoate | IUPAC |
| D-histidine monocation | JCBN |
| D-histidinium(1+) | JCBN |
| Registry Numbers | Sources |
|---|---|
| Gmelin:279474 | Gmelin |