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ChEBI
> Main
CHEBI:16731 - (
E
)-cinnamaldehyde
Main
ChEBI Ontology
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ChEBI Name
(
E
)-cinnamaldehyde
ChEBI ID
CHEBI:16731
ChEBI ASCII Name
(E)-cinnamaldehyde
Definition
The
E
(
trans
) stereoisomer of cinnamaldehyde, the parent of the class of cinnamaldehydes.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:181858, CHEBI:3709, CHEBI:13994, CHEBI:23244
Supplier Information
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Wikipedia
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Read full article at Wikipedia
Formula
C9H8O
Net Charge
0
Average Mass
132.15920
Monoisotopic Mass
132.05751
InChI
InChI=1S/C9H8O/c10-8-4-7-9-5-2-1-3-6-9/h1-8H/b7-4+
InChIKey
KJPRLNWUNMBNBZ-QPJJXVBHSA-N
SMILES
O=C\C=C\c1ccccc1
Roles Classification
Biological Role
(s):
sensitiser
A chemical compound that causes a substantial proportion of exposed people or animals to develop an allergic reaction in normal tissue after repeated exposure to the compound.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
EC 4.3.1.24 (phenylalanine ammonia-lyase) inhibitor
An EC 4.3.* (
C
1
N
lyase) inhibitor that interferes with the action of phenylalanine ammonia-lyase (EC 4.3.1.24).
antifungal agent
An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
flavouring agent
A food additive that is used to added improve the taste or odour of a food.
Application
(s):
hypoglycemic agent
A drug which lowers the blood glucose level.
vasodilator agent
A drug used to cause dilation of the blood vessels.
flavouring agent
A food additive that is used to added improve the taste or odour of a food.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
(
E
)-cinnamaldehyde (
CHEBI:16731
)
has role
antifungal agent (
CHEBI:35718
)
(
E
)-cinnamaldehyde (
CHEBI:16731
)
has role
EC 4.3.1.24 (phenylalanine ammonia-lyase) inhibitor (
CHEBI:62871
)
(
E
)-cinnamaldehyde (
CHEBI:16731
)
has role
flavouring agent (
CHEBI:35617
)
(
E
)-cinnamaldehyde (
CHEBI:16731
)
has role
hypoglycemic agent (
CHEBI:35526
)
(
E
)-cinnamaldehyde (
CHEBI:16731
)
has role
plant metabolite (
CHEBI:76924
)
(
E
)-cinnamaldehyde (
CHEBI:16731
)
has role
sensitiser (
CHEBI:139492
)
(
E
)-cinnamaldehyde (
CHEBI:16731
)
has role
vasodilator agent (
CHEBI:35620
)
(
E
)-cinnamaldehyde (
CHEBI:16731
)
is a
3-phenylprop-2-enal (
CHEBI:142921
)
(
E
)-cinnamaldehyde (
CHEBI:16731
)
is a
cinnamaldehydes (
CHEBI:23245
)
Incoming
α-hexylcinnamaldehyde (
CHEBI:55365
)
has functional parent
(
E
)-cinnamaldehyde (
CHEBI:16731
)
(
E
)-sinapaldehyde (
CHEBI:27949
)
has functional parent
(
E
)-cinnamaldehyde (
CHEBI:16731
)
3,4-dimethoxy cinnamaldehyde (
CHEBI:86548
)
has functional parent
(
E
)-cinnamaldehyde (
CHEBI:16731
)
4-acetoxy-3-methoxy-
trans
-cinnamaldehyde (
CHEBI:86579
)
has functional parent
(
E
)-cinnamaldehyde (
CHEBI:16731
)
4-hydroxycinnamaldehyde (
CHEBI:28353
)
has functional parent
(
E
)-cinnamaldehyde (
CHEBI:16731
)
4-methoxymagnaldehyde B (
CHEBI:66705
)
has functional parent
(
E
)-cinnamaldehyde (
CHEBI:16731
)
coniferyl aldehyde (
CHEBI:16547
)
has functional parent
(
E
)-cinnamaldehyde (
CHEBI:16731
)
IUPAC Name
(3
E
)-3-phenylprop-2-enal
Synonyms
Sources
(E)-3-Phenyl-2-propenal
ChemIDplus
(E)-3-Phenyl-propenal
ChEMBL
(E)-3-Phenylpropenal
ChemIDplus
(E)-Cinnamaldehyde
ChemIDplus
(
E
)-cinnamaldehyde
UniProt
(E)-Cinnamic aldehyde
NIST Chemistry WebBook
(E)-phenylvinyl aldehyde
ChEMBL
3-phenylacrylaldehyde
ChEBI
Cinnamaldehyde
KEGG COMPOUND
trans-Cinnamic aldehyde
ChemIDplus
Manual Xrefs
Databases
1069
BPDB
C00002725
KNApSAcK
C00035187
KNApSAcK
C00903
KEGG COMPOUND
Cinnamaldehyde
Wikipedia
HMDB0003441
HMDB
View more database links
Registry Numbers
Types
Sources
1071571
Beilstein Registry Number
ChemIDplus
1071571
Reaxys Registry Number
Reaxys
14371-10-9
CAS Registry Number
ChemIDplus
14371-10-9
CAS Registry Number
NIST Chemistry WebBook
Citations
Types
Sources
11975643
PubMed citation
Europe PMC
17140783
PubMed citation
Europe PMC
17662960
PubMed citation
Europe PMC
18218683
PubMed citation
Europe PMC
19845671
PubMed citation
Europe PMC
20431333
PubMed citation
Europe PMC
20955755
PubMed citation
Europe PMC
21266172
PubMed citation
Europe PMC
21388814
PubMed citation
Europe PMC
21394803
PubMed citation
Europe PMC
21466812
PubMed citation
Europe PMC
21469739
PubMed citation
Europe PMC
21517069
PubMed citation
Europe PMC
21603596
PubMed citation
Europe PMC
21708228
PubMed citation
Europe PMC
21767279
PubMed citation
Europe PMC
21788726
PubMed citation
Europe PMC
29079364
PubMed citation
Europe PMC
Last Modified
16 January 2019