CHEBI:16433 - trans-caffeic acid

ChEBI IDCHEBI:16433
ChEBI Nametrans-caffeic acid
Stars
ASCII Nametrans-caffeic acid
DefinitionThe trans-isomer of caffeic acid.
Secondary ChEBI IDsCHEBI:1379, CHEBI:11691, CHEBI:11692, CHEBI:12870, CHEBI:19877, CHEBI:41964
Last Modified21 October 2024
DownloadsMolfile
FormulaC9H8O4
Net Charge0
Average Mass180.159
Monoisotopic Mass180.04226
SMILESO=C(O)/C=C/c1ccc(O)c(O)c1
InChIInChI=1S/C9H8O4/c10-7-3-1-6(5-8(7)11)2-4-9(12)13/h1-5,10-11H,(H,12,13)/b4-2+
InChIKeyQAIPRVGONGVQAS-DUXPYHPUSA-N
Wikipedia
Species of MetaboliteComponentSourceComments
Solanum campaniforme (IPNI:818569-1) leaf (BTO:0000713) PubMed (21962208) Dried leaves were extracted with ethyl alcohol.
Mus musculus (ncbitaxon:10090) - PubMed (19425150) Source: BioModels - MODEL1507180067
Roles Classification
Chemical Roles:
antioxidant  A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Roles:
mouse metabolite  Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
EC 1.13.11.34 (arachidonate 5-lipoxygenase) inhibitor  A lipoxygenase inhibitor that interferes with the action of arachidonate 5-lipoxygenase (EC 1.13.11.34).
EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor  A lipoxygenase inhibitor that interferes with the action of arachidonate 15-lipoxygenase (EC 1.13.11.33).
EC 2.5.1.18 (glutathione transferase) inhibitor  An EC 2.5.1.* (non-methyl-alkyl or aryl transferase) inhibitor that interferes with the action of a glutathione transferase (EC 2.5.1.18).
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
EC 3.5.1.98 (histone deacetylase) inhibitor  An EC 3.5.1.* (non-peptide linear amide C-N hydrolase) inhibitor that interferes with the function of histone deacetylase (EC 3.5.1.98).
Application:
geroprotector  Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.
ChEBI Ontology
Outgoing Relation(s)
trans-caffeic acid (CHEBI:16433) has role geroprotector (CHEBI:176497)
trans-caffeic acid (CHEBI:16433) has role mouse metabolite (CHEBI:75771)
trans-caffeic acid (CHEBI:16433) is a caffeic acid (CHEBI:36281)
trans-caffeic acid (CHEBI:16433) is conjugate acid of trans-caffeate (CHEBI:57770)
Incoming Relation(s)
(2S,3R)-trans-caftaric acid (CHEBI:76075) has functional parent trans-caffeic acid (CHEBI:16433)
Cuscuta propenamide 1 (CHEBI:65700) has functional parent trans-caffeic acid (CHEBI:16433)
N-caffeoylspermidine (CHEBI:138030) has functional parent trans-caffeic acid (CHEBI:16433)
N1,N5,N10-tris-(E)-caffeoyl spermidine (CHEBI:232324) has functional parent trans-caffeic acid (CHEBI:16433)
N1,N8-bis(caffeoyl)spermidine (CHEBI:138028) has functional parent trans-caffeic acid (CHEBI:16433)
trans-5-O-caffeoyl-D-quinic acid (CHEBI:16384) has functional parent trans-caffeic acid (CHEBI:16433)
trans-caffeoyl-CoA (CHEBI:87449) has functional parent trans-caffeic acid (CHEBI:16433)
1-O-caffeoylquinic acid (CHEBI:136555) has functional parent trans-caffeic acid (CHEBI:16433)
1-caffeoyl-5-feruloylquinic acid (CHEBI:88343) has functional parent trans-caffeic acid (CHEBI:16433)
1-caffeoyl-β-D-glucose (CHEBI:614) has functional parent trans-caffeic acid (CHEBI:16433)
1,3-dicaffeoylquinic acid (CHEBI:520) has functional parent trans-caffeic acid (CHEBI:16433)
1,3,4,5-tetracaffeoylquinic acid (CHEBI:512) has functional parent trans-caffeic acid (CHEBI:16433)
2-O-caffeoyl maslinic acid (CHEBI:65547) has functional parent trans-caffeic acid (CHEBI:16433)
3-O-β-D-glucosyl-trans-caffeic acid (CHEBI:3293) has functional parent trans-caffeic acid (CHEBI:16433)
3,4-dihydroxy-5-prenylcinnamic acid (CHEBI:65784) has functional parent trans-caffeic acid (CHEBI:16433)
3,5-di-O-caffeoyl quinic acid (CHEBI:65751) has functional parent trans-caffeic acid (CHEBI:16433)
4-O-trans-caffeoylquinic acid (CHEBI:75491) has functional parent trans-caffeic acid (CHEBI:16433)
4-O-β-D-glucosyl-trans-caffeic acid (CHEBI:142393) has functional parent trans-caffeic acid (CHEBI:16433)
5-[(E)-caffeoyl]shikimic acid (CHEBI:2106) has functional parent trans-caffeic acid (CHEBI:16433)
7-O-[6-(6-methoxycaffeoyl)glucosyl]isovitexin (CHEBI:75420) has functional parent trans-caffeic acid (CHEBI:16433)
acteoside (CHEBI:132853) has functional parent trans-caffeic acid (CHEBI:16433)
caffeic acid 3-sulfate (CHEBI:90242) has functional parent trans-caffeic acid (CHEBI:16433)
caffeic acid 3-sulfate(2−) (CHEBI:133740) has functional parent trans-caffeic acid (CHEBI:16433)
caffeoylglycolic acid methyl ester (CHEBI:65548) has functional parent trans-caffeic acid (CHEBI:16433)
calabricoside B (CHEBI:65551) has functional parent trans-caffeic acid (CHEBI:16433)
chlorogenic acid (CHEBI:16112) has functional parent trans-caffeic acid (CHEBI:16433)
ethyl trans-caffeate (CHEBI:132714) has functional parent trans-caffeic acid (CHEBI:16433)
evolvoid A (CHEBI:65890) has functional parent trans-caffeic acid (CHEBI:16433)
gelsemiol-6'-trans-caffeoyl-1-glucoside (CHEBI:65957) has functional parent trans-caffeic acid (CHEBI:16433)
litseaefoloside C (CHEBI:66582) has functional parent trans-caffeic acid (CHEBI:16433)
malvidin 3-O-{6-O-[(E)-caffeoyl]-β-D-glucoside} (CHEBI:131453) has functional parent trans-caffeic acid (CHEBI:16433)
methyl 3,4-dicaffeoylquinate (CHEBI:85153) has functional parent trans-caffeic acid (CHEBI:16433)
quercetin 3-O-[(6-O-caffeoyl-β-D-glucosyl)-(1→2)-β-D-glucoside] (CHEBI:145787) has functional parent trans-caffeic acid (CHEBI:16433)
quercetin 3-O-α-(6'''-caffeoylglucosyl-β-1,2-rhamnoside) (CHEBI:66284) has functional parent trans-caffeic acid (CHEBI:16433)
rosmarinic acid (CHEBI:17226) has functional parent trans-caffeic acid (CHEBI:16433)
subulatin (CHEBI:66533) has functional parent trans-caffeic acid (CHEBI:16433)
trans-caffeate (CHEBI:57770) is conjugate base of trans-caffeic acid (CHEBI:16433)
IUPAC Name 
(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid
Synonyms  Source
3,4-Dihydroxy-trans-cinnamateKEGG COMPOUND
trans-CaffeateKEGG COMPOUND
3,4-dihydroxy-trans-cinnamateChEBI
trans-caffeateChEBI
CAFFEIC ACIDPDBeChem
3,4-Dihydroxy-trans-cinnamateKEGG COMPOUND
Manual XrefsDatabases
C01197KEGG COMPOUND
DHCPDBeChem
Caffeic_acidWikipedia
HMDB0001964HMDB
C00000615KNApSAcK
C01481KEGG COMPOUND
Registry NumbersSources
Reaxys:1954563Reaxys
CAS:501-16-6KEGG COMPOUND
CAS:501-16-6ChemIDplus
CAS:331-39-5KEGG COMPOUND
Citations