CHEBI:15400 - (−)-carvone

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (−)-carvone
ChEBI ID CHEBI:15400
ChEBI ASCII Name (-)-carvone
Definition A carvone having (R) configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:10775, CHEBI:18480, CHEBI:86
Supplier Information
Download Molfile XML SDF
Formula C10H14O
Net Charge 0
Average Mass 150.21756
Monoisotopic Mass 150.10447
InChI InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m1/s1
InChIKey ULDHMXUKGWMISQ-SECBINFHSA-N
SMILES CC(=C)[C@@H]1CC=C(C)C(=O)C1
Roles Classification
Biological Role(s): allergen
A chemical compound, or part thereof, which causes the onset of an allergic reaction by interacting with any of the molecular pathways involved in an allergy.
(via carvone )
antifungal agent
An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
(via botanical anti-fungal agent )
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via botanical anti-fungal agent )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (−)-carvone (CHEBI:15400) is a carvone (CHEBI:38265)
(−)-carvone (CHEBI:15400) is enantiomer of (+)-carvone (CHEBI:15399)
Incoming (5R)-5-isopropenyl-1,2-dimethylcyclohexane 1-hydroperoxide (CHEBI:59624) has functional parent (−)-carvone (CHEBI:15400)
(+)-carvone (CHEBI:15399) is enantiomer of (−)-carvone (CHEBI:15400)
IUPAC Names
(4R)-p-mentha-1(6),8-dien-2-one
(5R)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one
Synonyms Sources
(−)-(4R)-carvone ChEBI
(−)-(R)-carvone NIST Chemistry WebBook
(−)-p-mentha-6,8-dien-2-one NIST Chemistry WebBook
(-)-Carvone KEGG COMPOUND
(4R)-Carvone KEGG COMPOUND
(5R)-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-one ChemIDplus
(R)-(−)-carvone NIST Chemistry WebBook
(R)-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-one ChemIDplus
(R)-5-isopropenyl-2-methylcyclohex-2-en-1-one ChEBI
(R)-carvone UniProt
l-1-methyl-4-isopropenyl-6-cyclohexen-2-one NIST Chemistry WebBook
l-carvone ChemIDplus
l-p-mentha-1(6),8-dien-2-one ChemIDplus
levo-carvone NIST Chemistry WebBook
Manual Xrefs Databases
125 PPDB
C00000807 KNApSAcK
C01767 KEGG COMPOUND
c0627 UM-BBD
LMPR0102090007 LIPID MAPS
View more database links
Registry Numbers Types Sources
2206714 Reaxys Registry Number Reaxys
2206714 Beilstein Registry Number Beilstein
3588497 Beilstein Registry Number Beilstein
6485-40-1 CAS Registry Number KEGG COMPOUND
6485-40-1 CAS Registry Number NIST Chemistry WebBook
6485-40-1 CAS Registry Number ChemIDplus
83213 Gmelin Registry Number Gmelin
Citation Waiting for Citations Type Source
11380545 PubMed citation Europe PMC
Last Modified
18 September 2018
General Comment
2011-03-09 Distinghishable from its (+)-enantiomer by its spearmint taste and smell.