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CHEBI:50233 - (+)-isodihydrocarveol

ChEBI IDCHEBI:50233
ChEBI Name(+)-isodihydrocarveol
Stars
DefinitionThe (1S,2S,4R)-stereoisomer of dihydrocarveol.
Secondary ChEBI IDsCHEBI:161, CHEBI:50227
Last Modified24 June 2014
SubmitterMarcus Ennis
DownloadsMolfile
FormulaC10H18O
Net Charge0
Average Mass154.253
Monoisotopic Mass154.13577
SMILESC=C(C)[C@@H]1CC[C@H](C)[C@@H](O)C1
InChIInChI=1S/C10H18O/c1-7(2)9-5-4-8(3)10(11)6-9/h8-11H,1,4-6H2,2-3H3/t8-,9+,10-/m0/s1
InChIKeyKRCZYMFUWVJCLI-AEJSXWLSSA-N
Roles Classification
Biological Roles:
volatile oil component  Any plant metabolite that is found naturally as a component of a volatile oil.
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Application:
acaricide  A substance used to destroy pests of the subclass Acari (mites and ticks).
ChEBI Ontology
Outgoing Relation(s)
(+)-isodihydrocarveol (CHEBI:50233) is a dihydrocarveol (CHEBI:50215)
(+)-isodihydrocarveol (CHEBI:50233) is enantiomer of (−)-isodihydrocarveol (CHEBI:150)
Incoming Relation(s)
(−)-isodihydrocarveol (CHEBI:150) is enantiomer of (+)-isodihydrocarveol (CHEBI:50233)
IUPAC Names 
(1S,2S,5R)-2-methyl-5-(prop-1-en-2-yl)cyclohexanol
(1S,2S,4R)-p-menth-8-en-2-ol
Synonyms  Source
(1S,2S,4R)-Iso-dihydrocarveolKEGG COMPOUND
(1S,2S,5R)-5-isopropenyl-2-methylcyclohexanolChEBI
UniProt Name  Source
(1S,2S,4R)-isodihydrocarveolUniProt
Manual XrefsDatabases
C11399KEGG COMPOUND
LMPR0102090034LIPID MAPS
Registry NumbersSources
Beilstein:2553476Beilstein
Reaxys:2553476Reaxys