CHEBI:232 - (+)-cis-carveol

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ChEBI Name (+)-cis-carveol
ChEBI ID CHEBI:232
ChEBI ASCII Name (+)-cis-carveol
Definition The (1S,5S)-stereoisomer of carveol.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C10H16O
Net Charge 0
Average Mass 152.23344
Monoisotopic Mass 152.12012
InChI InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3/t9-,10-/m0/s1
InChIKey BAVONGHXFVOKBV-UWVGGRQHSA-N
SMILES CC(=C)[C@H]1CC=C(C)[C@@H](O)C1
Roles Classification
Biological Role(s): volatile oil component
Any plant metabolite that is found naturally as a component of a volatile oil.
(via carveol )
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via carveol )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (+)-cis-carveol (CHEBI:232) is a carveol (CHEBI:23046)
(+)-cis-carveol (CHEBI:232) is enantiomer of (−)-cis-carveol (CHEBI:227)
Incoming (−)-cis-carveol (CHEBI:227) is enantiomer of (+)-cis-carveol (CHEBI:232)
IUPAC Names
(1S,5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-ol
(4S,6S)-p-mentha-1,8-dien-6-ol
Synonyms Sources
(+)-(4S,6S)-cis-carveol ChEBI
(1S,5S)-carveol UniProt
(4S,6S)-cis-Carveol KEGG COMPOUND
Manual Xref Database
C11408 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
2206716 Reaxys Registry Number Reaxys
2206716 Beilstein Registry Number Beilstein
Last Modified
29 January 2015