5-hydroxyindoleacetylglycine (CHEBI:27631)

ChEBI > Main

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name	5-hydroxyindoleacetylglycine

ChEBI ID	CHEBI:27631

Definition	An N-acylglycine resulting from the formal condensation of the carboxy group of (5-hydroxyindol-3-yl)acetic acid with the amino group of glycine.

Stars	This entity has been manually annotated by the ChEBI Team.

Secondary ChEBI IDs	CHEBI:20586, CHEBI:2072

Supplier Information

Download	Molfile XML SDF

Formula

C12H12N2O4

Net Charge

Average Mass

248.238

Monoisotopic Mass

248.07971

InChI

InChI=1S/C12H12N2O4/c15-8-1-2-10-9(4-8)7(5-13-10)3-11(16)14-6-12(17)18/h1-2,4-5,13,15H,3,6H2,(H,14,16)(H,17,18)

InChIKey

LFUCRBSGQMAKCO-UHFFFAOYSA-N

SMILES

OC(=O)CNC(=O)CC1=CNC2=CC=C(O)C=C12

Metabolite of Species	Details
Rattus norvegicus (NCBI:txid10116)	Found in urine (BTO:0001419). 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):	rat metabolite Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus).

ChEBI Ontology
Outgoing	5-hydroxyindoleacetylglycine (CHEBI:27631) has functional parent (5-hydroxyindol-3-yl)acetic acid (CHEBI:27823) 5-hydroxyindoleacetylglycine (CHEBI:27631) has role rat metabolite (CHEBI:86264) 5-hydroxyindoleacetylglycine (CHEBI:27631) is a N-acylglycine (CHEBI:16180) 5-hydroxyindoleacetylglycine (CHEBI:27631) is a hydroxyindoles (CHEBI:84729)

IUPAC Name

N-[(5-hydroxy-1H-indol-3-yl)acetyl]glycine

Synonyms	Sources
2-[2-(5-hydroxy-1H-indol-3-yl)acetamido]acetic acid	IUPAC
5-hydroxyindoleacetyl glycine	ChEBI
5-hydroxyindoleacetylglycine	KEGG COMPOUND
N-[(5-hydroxyindol-3-yl)acetyl]-glycine	ChEBI

Registry Number	Type	Source
16606-62-5	CAS Registry Number	ChEBI

Last Modified

02 March 2021