EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C5H10O6 |
| Net Charge | 0 |
| Average Mass | 166.129 |
| Monoisotopic Mass | 166.04774 |
| SMILES | O=C(O)[C@H](O)[C@@H](O)[C@H](O)CO |
| InChI | InChI=1S/C5H10O6/c6-1-2(7)3(8)4(9)5(10)11/h2-4,6-9H,1H2,(H,10,11)/t2-,3+,4-/m1/s1 |
| InChIKey | QXKAIJAYHKCRRA-FLRLBIABSA-N |
| Wikipedia |
|---|
| Roles Classification |
|---|
| Chemical Role: | Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Brønsted base). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| D-xylonic acid (CHEBI:48093) is a xylonic acid (CHEBI:33828) |
| D-xylonic acid (CHEBI:48093) is conjugate acid of D-xylonate (CHEBI:17746) |
| D-xylonic acid (CHEBI:48093) is enantiomer of L-xylonic acid (CHEBI:48092) |
| Incoming Relation(s) |
| D-xylono-1,4-lactone (CHEBI:16392) has functional parent D-xylonic acid (CHEBI:48093) |
| D-xylono-1,5-lactone (CHEBI:15867) has functional parent D-xylonic acid (CHEBI:48093) |
| 5-phospho-D-xylonic acid (CHEBI:136746) has functional parent D-xylonic acid (CHEBI:48093) |
| D-xylonate (CHEBI:17746) is conjugate base of D-xylonic acid (CHEBI:48093) |
| L-xylonic acid (CHEBI:48092) is enantiomer of D-xylonic acid (CHEBI:48093) |
| IUPAC Names |
|---|
| (2R,3S,4R)-2,3,4,5-tetrahydroxypentanoic acid |
| D-xylonic acid |
| Synonym | Source |
|---|---|
| D-Xylonate | KEGG COMPOUND |
| Manual Xrefs | Databases |
|---|---|
| C00502 | KEGG COMPOUND |
| Xylonic_acid | Wikipedia |
| Registry Numbers | Sources |
|---|---|
| Beilstein:1724268 | Beilstein |
| CAS:526-91-0 | KEGG COMPOUND |