CHEBI:15420 - perillyl alcohol

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name perillyl alcohol
ChEBI ID CHEBI:15420
Definition A limonene monoterpenoid consists of a cyclohexene ring substituted by a hydroxymethyl and a prop-1-en-2-yl group at positions 1 and 4 respectively. It is a constituent of a variety of essential oils including lavender.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:18496, CHEBI:8022, CHEBI:14772
Supplier Information
Download Molfile XML SDF
Formula C10H16O
Net Charge 0
Average Mass 152.23344
Monoisotopic Mass 152.12012
InChI InChI=1S/C10H16O/c1-8(2)10-5-3-9(7-11)4-6-10/h3,10-11H,1,4-7H2,2H3
InChIKey NDTYTMIUWGWIMO-UHFFFAOYSA-N
SMILES CC(=C)C1CCC(CO)=CC1
Metabolite of Species Details
Homo sapiens (NCBI:txid9606) See: DOI
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
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 alcohol (CHEBI:15420) has role plant metabolite (CHEBI:76924)
perillyl alcohol (CHEBI:15420) has role volatile oil component (CHEBI:27311)
perillyl alcohol (CHEBI:15420) is a limonene monoterpenoid (CHEBI:25040)
Incoming (−)-perillyl alcohol (CHEBI:10782) is a perillyl alcohol (CHEBI:15420)
IUPAC Name
[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol
Synonyms Sources
1-Hydroxymethyl-4-isopropenyl-1-cyclohexene ChemIDplus
1-perillalcohol NIST Chemistry WebBook
4-(1-Methylethenyl)-1-cyclohexene-1-methanol ChemIDplus
4-Isopropenyl-1-cyclohexene carbinol ChemIDplus
4-Isopropenylcyclohex-1-en-1-ylmethanol ChemIDplus
dihydrocuminyl alcoholn NIST Chemistry WebBook
Isocarveol ChemIDplus
p-Mentha-1,8-dien-7-ol ChemIDplus
Perilla alcohol ChemIDplus
Perillol ChemIDplus
perillyl alcohol UniProt
Manual Xrefs Databases
HMDB0003634 HMDB
Perillyl-Alcohols MetaCyc
View more database links
Registry Numbers Types Sources
2044612 Reaxys Registry Number Reaxys
536-59-4 CAS Registry Number NIST Chemistry WebBook
536-59-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10379660 PubMed citation Europe PMC
11840288 PubMed citation Europe PMC
15210838 PubMed citation Europe PMC
23727191 PubMed citation Europe PMC
Last Modified
23 October 2015