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CHEBI:12876 - trans-4-coumarate

ChEBI IDCHEBI:12876
ChEBI Nametrans-4-coumarate
Stars
ASCII Nametrans-4-coumarate
DefinitionThe trans-isomer of 4-coumarate.
Last Modified18 July 2020
DownloadsMolfile
FormulaC9H7O3
Net Charge-1
Average Mass163.152
Monoisotopic Mass163.04007
SMILESO=C([O-])/C=C/c1ccc(O)cc1
InChIInChI=1S/C9H8O3/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-6,10H,(H,11,12)/p-1/b6-3+
InChIKeyNGSWKAQJJWESNS-ZZXKWVIFSA-M
Species of MetaboliteComponentSourceComments
Homo sapiens (ncbitaxon:9606) - DOI (10.1038/nbt.2488)
Roles Classification
Biological Roles:
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
ChEBI Ontology
Outgoing Relation(s)
trans-4-coumarate (CHEBI:12876) has role plant metabolite (CHEBI:76924)
trans-4-coumarate (CHEBI:12876) is a 4-coumarate (CHEBI:32373)
trans-4-coumarate (CHEBI:12876) is conjugate base of trans-4-coumaric acid (CHEBI:32374)
Incoming Relation(s)
trans-4-coumaroyl-AMP(1−) (CHEBI:192348) has functional parent trans-4-coumarate (CHEBI:12876)
trans-4-coumaric acid (CHEBI:32374) is conjugate acid of trans-4-coumarate (CHEBI:12876)
IUPAC Name 
(2E)-3-(4-hydroxyphenyl)prop-2-enoate
Synonyms  Source
(2E)-3-(4-hydroxyphenyl)acrylateChEBI
trans-p-coumarateChEBI
UniProt Name  Source
(E)-4-coumarateUniProt
Manual XrefsDatabases
COUMARATEMetaCyc
Registry NumbersSources
Gmelin:2148756Gmelin
Reaxys:5513651Reaxys