CHEBI:65331 - alkyl caffeate ester

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ChEBI Name alkyl caffeate ester
ChEBI ID CHEBI:65331
Definition A cinnamate ester obtained by formal condensation of caffeic acid with any alkyl alcohol.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter T. Berardini
Download Molfile XML SDF
Formula C9H7O4R
Net Charge 0
Average Mass (excl. R groups) 179.150
Monoisotopic Mass (excl. R groups) 179.03443
SMILES C=1(C=CC(=C(C1)O)O)/C=C/C(O*)=O
ChEBI Ontology
Outgoing alkyl caffeate ester (CHEBI:65331) has functional parent caffeic acid (CHEBI:36281)
alkyl caffeate ester (CHEBI:65331) is a catechols (CHEBI:33566)
alkyl caffeate ester (CHEBI:65331) is a cinnamate ester (CHEBI:36087)
alkyl caffeate ester (CHEBI:65331) is a phenylpropanoid (CHEBI:26004)
Incoming β-(4-hydroxyphenyl)ethyl-4-O-E-caffeoyl-O-[β-D-apiofuranosyl-(1→2)]-β-D-glucopyranoside (CHEBI:68340) is a alkyl caffeate ester (CHEBI:65331)
(3R,5R)-3,4,5-tris{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1-hydroxycyclohexane-1-carboxylic acid (CHEBI:139424) is a alkyl caffeate ester (CHEBI:65331)
(S)-1'-methylbutyl caffeate (CHEBI:70482) is a alkyl caffeate ester (CHEBI:65331)
(S)-1'-methylhexyl caffeate (CHEBI:70483) is a alkyl caffeate ester (CHEBI:65331)
(S)-1'-methyloctyl caffeate (CHEBI:70484) is a alkyl caffeate ester (CHEBI:65331)
1,3-dicaffeoylquinic acid (CHEBI:520) is a alkyl caffeate ester (CHEBI:65331)
1-O-caffeoylquinic acid (CHEBI:136555) is a alkyl caffeate ester (CHEBI:65331)
ethyl trans-caffeate (CHEBI:132714) is a alkyl caffeate ester (CHEBI:65331)
methyl 3,4-dicaffeoylquinate (CHEBI:85153) is a alkyl caffeate ester (CHEBI:65331)
methyl caffeate (CHEBI:6856) is a alkyl caffeate ester (CHEBI:65331)
monocaffeoylaltraric acid (CHEBI:147327) is a alkyl caffeate ester (CHEBI:65331)
phenethyl caffeate (CHEBI:8062) is a alkyl caffeate ester (CHEBI:65331)
subulatin (CHEBI:66533) is a alkyl caffeate ester (CHEBI:65331)
Synonym Source
alkyl caffeate ChEBI
Citation Waiting for Citations Type Source
22797656 PubMed citation SUBMITTER
Last Modified
03 December 2019