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CHEBI:65665 - trans-N-p-coumaroyl tyramine

ChEBI IDCHEBI:65665
ChEBI Nametrans-N-p-coumaroyl tyramine
Stars
DefinitionA natural product found particularly in Solanum melongena and Asimina triloba.
Last Modified2 April 2025
DownloadsMolfile
FormulaC17H17NO3
Net Charge0
Average Mass283.327
Monoisotopic Mass283.12084
SMILESO=C(/C=C/c1ccc(O)cc1)NCCc1ccc(O)cc1
InChIInChI=1S/C17H17NO3/c19-15-6-1-13(2-7-15)5-10-17(21)18-12-11-14-3-8-16(20)9-4-14/h1-10,19-20H,11-12H2,(H,18,21)/b10-5+
InChIKeyRXGUTQNKCXHALN-BJMVGYQFSA-N
Species of MetaboliteComponentSourceComments
Celtis chinensis (IPNI:851023-1) twig (BTO:0001411) PubMed (14560923)
Solanum melongena (ncbitaxon:4111) root (BTO:0001188) DOI (10.1271/bbb1961.42.623)
Asimina triloba (ncbitaxon:12953) bark (BTO:0001301) PubMed (1593281)
Arcangelisia gusanlung (ncbitaxon:432629) stem (BTO:0001300) PubMed (21500777) MeOH extract of air-dried and smashed stems
Nicotiana attenuata (ncbitaxon:49451) - MetaboLights (MTBLS335) From MetaboLights
Roles Classification
Chemical Role:
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
ChEBI Ontology
Outgoing Relation(s)
trans-N-p-coumaroyl tyramine (CHEBI:65665) has role metabolite (CHEBI:25212)
trans-N-p-coumaroyl tyramine (CHEBI:65665) is a hydroxycinnamic acid (CHEBI:24689)
Synonyms  Source
(E)-3-(4-hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamideChEBI
(2E)-3-(4-Hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]acrylamideChEBI
N-(4-hydroxy-beta-phenethyl)-4-hydroxycinnamideChEBI
UniProt Name  Source
N-[(E)-4-coumaroyl]tyramineUniProt
Manual XrefsDatabases
HMDB0039521HMDB
Citations