CHEBI:27480 - phenylacetylglycine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name phenylacetylglycine
Definition A N-acylglycine that is glycine substituted on nitrogen with a phenylacetyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:25983, CHEBI:8088, CHEBI:613592
Supplier Information
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Formula C10H11NO3
Net Charge 0
Average Mass 193.19920
Monoisotopic Mass 193.07389
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)
SMILES OC(=O)CNC(=O)Cc1ccccc1
Metabolite of Species Details
Mus musculus (NCBI:txidtxid10090) See: PubMed
Mus musculus (NCBI:txidtxid10090) Source: BioModels - MODEL1507180067 See: PubMed
Homo sapiens (NCBI:txidtxid9606) See: PubMed
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 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 4-hydroxyphenylacetylglycine (CHEBI:28595) has functional parent phenylacetylglycine (CHEBI:27480)
phenylacetylglycine(1−) (CHEBI:60874) is conjugate base of phenylacetylglycine (CHEBI:27480)
Synonyms Sources
N-Phenacetylglycine ChemIDplus
N-Phenylacetylglycine ChemIDplus
Phenaceturic acid ChEMBL
Phenacetylglycine ChEBI
Phenylacetylglycine KEGG COMPOUND
Manual Xrefs Databases
CPD-11715 MetaCyc
HMDB0000821 HMDB
View more database links
Registry Numbers Types Sources
1107116 Reaxys Registry Number Reaxys
500-98-1 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
15764292 PubMed citation Europe PMC
19961175 PubMed citation Europe PMC
21167146 PubMed citation Europe PMC
22770225 PubMed citation Europe PMC
22935565 PubMed citation Europe PMC
Last Modified
27 January 2016