CHEBI:17818 - N-feruloyltyramine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name N-feruloyltyramine
ChEBI ID CHEBI:17818
ChEBI ASCII Name N-feruloyltyramine
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:12500, CHEBI:7272, CHEBI:21701
Supplier Information
Download Molfile XML SDF
Formula C18H19NO4
Net Charge 0
Average Mass 313.34780
Monoisotopic Mass 313.13141
InChI InChI=1S/C18H19NO4/c1-23-17-12-14(4-8-16(17)21)5-9-18(22)19-11-10-13-2-6-15(20)7-3-13/h2-9,12,20-21H,10-11H2,1H3,(H,19,22)/b9-5+
InChIKey NPNNKDMSXVRADT-WEVVVXLNSA-N
SMILES COc1cc(\C=C\C(=O)NCCc2ccc(O)cc2)ccc1O
Metabolite of Species Details
Piper boehmeriaefolium (NCBI:txid130389) Found in whole plant (BTO:0001461). Methanolic extract of air-dried, powdered whole plant See: PubMed
Pisonia aculeata (NCBI:txid363212) Found in stem (BTO:0001300). Cold methanolic extract of dried stems and roots See: PubMed
Pisonia aculeata (NCBI:txid363212) Found in root (BTO:0001188). Cold methanolic extract of dried stems and roots 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): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing N-feruloyltyramine (CHEBI:17818) has role metabolite (CHEBI:25212)
N-feruloyltyramine (CHEBI:17818) is a tyramines (CHEBI:27175)
IUPAC Name
(2E)-3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide
Synonyms Sources
Moupinamide ChemIDplus
N-[(E)-feruloyl]tyramine UniProt
N-Feruloyltyramine KEGG COMPOUND
trans-N-Feruloyltyramine KEGG COMPOUND
Manual Xrefs Databases
C00000660 KNApSAcK
C02717 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
65646-26-6 CAS Registry Number ChemIDplus
66648-43-9 CAS Registry Number KEGG COMPOUND
Last Modified
09 August 2019