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CHEBI:27480 - phenylacetylglycine
| Formula | C10H11NO3 |
| Net Charge | 0 |
| Average Mass | 193.202 |
| Monoisotopic Mass | 193.07389 |
| SMILES | O=C(O)CNC(=O)Cc1ccccc1 |
| InChI | InChI=1S/C10H11NO3/c12-9(11-7-10(13)14)6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,11,12)(H,13,14) |
| InChIKey | UTYVDVLMYQPLQB-UHFFFAOYSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Mus musculus (ncbitaxon:10090) | |||
| - | PubMed (19961175) | ||
| - | PubMed (19425150) | Source: BioModels - MODEL1507180067 | |
| Homo sapiens (ncbitaxon:9606) | - | PubMed (21167146) |
| Roles Classification |
|---|
| Chemical Role: | Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Brønsted base). |
| Biological Roles: | human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| phenylacetylglycine (CHEBI:27480) has role human metabolite (CHEBI:77746) |
| phenylacetylglycine (CHEBI:27480) has role mouse metabolite (CHEBI:75771) |
| phenylacetylglycine (CHEBI:27480) is a N-acylglycine (CHEBI:16180) |
| phenylacetylglycine (CHEBI:27480) is a monocarboxylic acid (CHEBI:25384) |
| phenylacetylglycine (CHEBI:27480) is a monocarboxylic acid amide (CHEBI:29347) |
| phenylacetylglycine (CHEBI:27480) is conjugate acid of phenylacetylglycine(1−) (CHEBI:60874) |
| Incoming Relation(s) |
| 4-hydroxyphenylacetylglycine (CHEBI:28595) has functional parent phenylacetylglycine (CHEBI:27480) |
| phenylacetylglycine(1−) (CHEBI:60874) is conjugate base of phenylacetylglycine (CHEBI:27480) |
| IUPAC Name |
|---|
| N-(phenylacetyl)glycine |
| Synonyms | Source |
|---|---|
| Phenylacetylglycine | KEGG COMPOUND |
| N-Phenacetylglycine | ChemIDplus |
| N-Phenylacetylglycine | ChemIDplus |
| Phenacetylglycine | ChEBI |
| Phenaceturic acid | ChEMBL |
| Manual Xrefs | Databases |
|---|---|
| C05598 | KEGG COMPOUND |
| HMDB0000821 | HMDB |
| CPD-11715 | MetaCyc |
| Registry Numbers | Sources |
|---|---|
| Reaxys:1107116 | Reaxys |
| CAS:500-98-1 | ChemIDplus |
| Citations |
|---|