EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C2H5NO2 |
| Net Charge | 0 |
| Average Mass | 75.067 |
| Monoisotopic Mass | 75.03203 |
| SMILES | CC(=O)NO |
| InChI | InChI=1S/C2H5NO2/c1-2(4)3-5/h5H,1H3,(H,3,4) |
| InChIKey | RRUDCFGSUDOHDG-UHFFFAOYSA-N |
| Wikipedia |
|---|
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Chlamydomonas reinhardtii (ncbitaxon:3055) | - | PubMed (25515814) |
| Roles Classification |
|---|
| Biological Roles: | EC 3.5.1.5 (urease) inhibitor EC 3.5.1.* (non-peptide linear amide C-N hydrolase) inhibitor that interferes with the activity of urease (EC 3.5.1.5), reducing hydrolysis. algal metabolite Any eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| acetohydroxamic acid (CHEBI:27777) has functional parent acetamide (CHEBI:27856) |
| acetohydroxamic acid (CHEBI:27777) has role algal metabolite (CHEBI:84735) |
| acetohydroxamic acid (CHEBI:27777) has role EC 3.5.1.5 (urease) inhibitor (CHEBI:50635) |
| acetohydroxamic acid (CHEBI:27777) is a acetohydroxamic acids (CHEBI:22177) |
| acetohydroxamic acid (CHEBI:27777) is tautomer of N-hydroxyacetimidic acid (CHEBI:49029) |
| Incoming Relation(s) |
| N-hydroxyacetimidic acid (CHEBI:49029) is tautomer of acetohydroxamic acid (CHEBI:27777) |
| IUPAC Name |
|---|
| N-hydroxyacetamide |
| INNs | Source |
|---|---|
| acetohydroxamic acid | ChemIDplus |
| acide acétohydroxamique | ChEBI |
| ácido acetohidroxámico | ChEBI |
| acidum acetohydroxamicum | ChEBI |
| Synonyms | Source |
|---|---|
| Acetohydroxamic acid | KEGG COMPOUND |
| N-Acetylhydroxylamine | ChemIDplus |
| N-Hydroxyacetamide | ChEBI |
| N-Acetyl hydroxyacetamide | ChemIDplus |
| AHA | ChemIDplus |
| Methylhydroxamic acid | ChemIDplus |
| Brand Name | Source |
|---|---|
| Lithostat | DrugBank |