EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C2H6NO6P |
| Net Charge | 0 |
| Average Mass | 171.045 |
| Monoisotopic Mass | 170.99327 |
| SMILES | O=C(COP(=O)(O)O)NO |
| InChI | InChI=1S/C2H6NO6P/c4-2(3-5)1-9-10(6,7)8/h5H,1H2,(H,3,4)(H2,6,7,8) |
| InChIKey | BAXHHWZKQZIJID-UHFFFAOYSA-N |
| Roles Classification |
|---|
| Biological Role: | EC 5.3.1.1 (triose-phosphate isomerase) inhibitor Any EC 5.3.1.* (intramolecular oxidoreductase interconverting aldoses and ketoses) inhibitor that interferes with the action of a triose-phosphate isomerase (EC 5.3.1.1). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| phosphoglycolohydroxamic acid (CHEBI:28475) has functional parent glycolic acid (CHEBI:17497) |
| phosphoglycolohydroxamic acid (CHEBI:28475) has role EC 5.3.1.1 (triose-phosphate isomerase) inhibitor (CHEBI:90691) |
| phosphoglycolohydroxamic acid (CHEBI:28475) is a amidoalkyl phosphate (CHEBI:37481) |
| phosphoglycolohydroxamic acid (CHEBI:28475) is a hydroxamic acid (CHEBI:24650) |
| IUPAC Name |
|---|
| 2-(hydroxyamino)-2-oxoethyl dihydrogen phosphate |
| Synonyms | Source |
|---|---|
| Phosphoglycolohydroxamate | KEGG COMPOUND |
| Phosphoglycolohydroxamic Acid | DrugBank |
| Registry Numbers | Sources |
|---|---|
| Reaxys:1870128 | Reaxys |
| CAS:51528-59-7 | ChemIDplus |
| Citations |
|---|