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InChI=1S/CH4O/c1-2/h2H,1H3
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> Main
CHEBI:15421 - perillyl aldehyde
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ChEBI Name
perillyl aldehyde
ChEBI ID
CHEBI:15421
Definition
An aldehyde that is cyclohex-1-ene-1-carbaldehyde substituted by a prop-1-en-2-yl group at position 4.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:14773, CHEBI:8023, CHEBI:25938
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Formula
C10H14O
Net Charge
0
Average Mass
150.21756
Monoisotopic Mass
150.10447
InChI
InChI=1S/C10H14O/c1-8(2)10-5-3-9(7-11)4-6-10/h3,7,10H,1,4-6H2,2H3
InChIKey
RUMOYJJNUMEFDD-UHFFFAOYSA-N
SMILES
[H]C(=O)C1=CCC(CC1)C(C)=C
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Homo sapiens
(NCBI:txid9606)
See:
DOI
Roles Classification
Biological Role
(s):
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
volatile oil component
Any plant metabolite that is found naturally as a component of a volatile oil.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
perillyl aldehyde (
CHEBI:15421
)
has role
human metabolite (
CHEBI:77746
)
perillyl aldehyde (
CHEBI:15421
)
has role
mouse metabolite (
CHEBI:75771
)
perillyl aldehyde (
CHEBI:15421
)
has role
volatile oil component (
CHEBI:27311
)
perillyl aldehyde (
CHEBI:15421
)
is a
aldehyde (
CHEBI:17478
)
perillyl aldehyde (
CHEBI:15421
)
is a
olefinic compound (
CHEBI:78840
)
IUPAC Name
4-(prop-1-en-2-yl)cyclohex-1-ene-1-carbaldehyde
Synonyms
Sources
4-(1-methylethenyl)-1-cyclohexene1-carboxyaldehyde
ChEBI
p
-mentha-1,8-dien-7-al
NIST Chemistry WebBook
perillal
NIST Chemistry WebBook
Perillaldehyde
KEGG COMPOUND
perillic aldehyde
ChemIDplus
Perillyl aldehyde
KEGG COMPOUND
perillyl aldehyde
UniProt
perillylaldehyde
ChEBI
Manual Xrefs
Databases
C00003050
KNApSAcK
C02576
KEGG COMPOUND
c0666
UM-BBD
LMPR0102090010
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
2111-75-3
CAS Registry Number
ChemIDplus
2111-75-3
CAS Registry Number
NIST Chemistry WebBook
Citation
Type
Source
23413567
PubMed citation
Europe PMC
Last Modified
27 January 2016