CHEBI:28715 - 5-hydroxykynurenamine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 5-hydroxykynurenamine
Definition A hydroxykynurenamine where the hydroxy group is located at the 5-position.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:20589, CHEBI:2075
Supplier Information
Download Molfile XML SDF
Formula C9H12N2O2
Net Charge 0
Average Mass 180.20380
Monoisotopic Mass 180.08988
InChI InChI=1S/C9H12N2O2/c10-4-3-9(13)7-5-6(12)1-2-8(7)11/h1-2,5,12H,3-4,10-11H2
SMILES NCCC(=O)c1cc(O)ccc1N
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5-hydroxykynurenamine (CHEBI:28715) has role mouse metabolite (CHEBI:75771)
5-hydroxykynurenamine (CHEBI:28715) is a hydroxykynurenamine (CHEBI:24705)
5-hydroxykynurenamine (CHEBI:28715) is conjugate base of 5-hydroxykynurenaminium(1+) (CHEBI:62214)
Incoming formyl-5-hydroxykynurenamine (CHEBI:28736) has functional parent 5-hydroxykynurenamine (CHEBI:28715)
5-hydroxykynurenaminium(1+) (CHEBI:62214) is conjugate acid of 5-hydroxykynurenamine (CHEBI:28715)
Synonyms Sources
3-Amino-1-(2-amino-5-hydroxyphenyl)-1-propanone ChemIDplus
5-Hydroxykynurenamine KEGG COMPOUND
Mausamine ChemIDplus
Mousamine ChemIDplus
Manual Xref Database
View more database links
Registry Numbers Types Sources
2093152 Reaxys Registry Number Reaxys
708-23-6 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
14468719 PubMed citation Europe PMC
4885724 PubMed citation Europe PMC
5049691 PubMed citation Europe PMC
5655081 PubMed citation Europe PMC
5861330 PubMed citation Europe PMC
Last Modified
27 January 2016