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CHEBI:232 - (+)-cis-carveol

Default Structure
ChEBI IDCHEBI:232
ChEBI Name(+)-cis-carveol
Stars
ASCII Name(+)-cis-carveol
DefinitionThe (1S,5S)-stereoisomer of carveol.
Last Modified29 January 2015
DownloadsMolfile
FormulaC10H16O
Net Charge0
Average Mass152.237
Monoisotopic Mass152.12012
SMILESC=C(C)[C@H]1CC=C(C)[C@@H](O)C1
InChIInChI=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
InChIKeyBAVONGHXFVOKBV-UWVGGRQHSA-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.
ChEBI Ontology
Outgoing Relation(s)
(+)-cis-carveol (CHEBI:232) is a carveol (CHEBI:23046)
(+)-cis-carveol (CHEBI:232) is enantiomer of (−)-cis-carveol (CHEBI:227)
Incoming Relation(s)
(−)-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  Source
(+)-(4S,6S)-cis-carveolChEBI
(4S,6S)-cis-CarveolKEGG COMPOUND
UniProt Name  Source
(1S,5S)-carveolUniProt
Manual XrefsDatabases
C11408KEGG COMPOUND
Registry NumbersSources
Reaxys:2206716Reaxys