CHEBI:15421 - perillyl aldehyde

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
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
Supplier Information
Download Molfile XML SDF
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 Waiting for Citations Type Source
23413567 PubMed citation Europe PMC
Last Modified
27 January 2016