CHEBI:15400 - (−)-carvone

ChEBI IDCHEBI:15400
ChEBI Name(−)-carvone
Stars
ASCII Name(-)-carvone
DefinitionA carvone having (R) configuration.
Secondary ChEBI IDsCHEBI:86, CHEBI:10775, CHEBI:18480
Last Modified18 September 2018
SubmitterMarcus Ennis
DownloadsMolfile
FormulaC10H14O
Net Charge0
Average Mass150.221
Monoisotopic Mass150.10447
SMILESC=C(C)[C@@H]1CC=C(C)C(=O)C1
InChIInChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m1/s1
InChIKeyULDHMXUKGWMISQ-SECBINFHSA-N
Roles Classification
Biological Roles:
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.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
ChEBI Ontology
Outgoing Relation(s)
(−)-carvone (CHEBI:15400) is a carvone (CHEBI:38265)
(−)-carvone (CHEBI:15400) is enantiomer of (+)-carvone (CHEBI:15399)
Incoming Relation(s)
(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  Source
(−)-(4R)-carvoneChEBI
(4R)-CarvoneKEGG COMPOUND
(5R)-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-oneChemIDplus
(-)-CarvoneKEGG COMPOUND
l-1-methyl-4-isopropenyl-6-cyclohexen-2-oneNIST Chemistry WebBook
l-carvoneChemIDplus
UniProt Name  Source
(R)-carvoneUniProt
Manual XrefsDatabases
125PPDB
C00000807KNApSAcK
C01767KEGG COMPOUND
c0627UM-BBD
LMPR0102090007LIPID MAPS
Registry NumbersSources
Reaxys:2206714Reaxys
Beilstein:3588497Beilstein
Gmelin:83213Gmelin
CAS:6485-40-1KEGG COMPOUND
CAS:6485-40-1ChemIDplus
CAS:6485-40-1NIST Chemistry WebBook
Citations