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CHEBI:26137 - pinocarveol

ChEBI IDCHEBI:26137
ChEBI Namepinocarveol
Stars
DefinitionA pinane monoterpenoid that is a bicyclo[3.1.1]heptane substituted by two methyl groups at position 6, a methylidene group at position 2 and a hydroxy group at position 3.
Secondary ChEBI IDCHEBI:29666
Last Modified27 January 2016
DownloadsMolfile
FormulaC10H16O
Net Charge0
Average Mass152.237
Monoisotopic Mass152.12012
SMILESC=C1C(O)CC2CC1C2(C)C
InChIInChI=1S/C10H16O/c1-6-8-4-7(5-9(6)11)10(8,2)3/h7-9,11H,1,4-5H2,2-3H3
InChIKeyLCYXQUJDODZYIJ-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Zingiber officinale (ncbitaxon:94328) - PubMed (20590154)
Mus musculus (ncbitaxon:10090) - PubMed (19425150) Source: BioModels - MODEL1507180067
Roles Classification
Biological Roles:
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
volatile oil component  Any plant metabolite that is found naturally as a component of a volatile oil.
GABA modulator  A substance that does not act as agonist or antagonist but does affect the gamma-aminobutyric acid receptor-ionophore complex. GABA-A receptors appear to have at least three allosteric sites at which modulators act: a site at which benzodiazepines act by increasing the opening frequency of gamma-aminobutyric acid-activated chloride channels; a site at which barbiturates act to prolong the duration of channel opening; and a site at which some steroids may act.
mouse metabolite  Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
Application:
GABA modulator  A substance that does not act as agonist or antagonist but does affect the gamma-aminobutyric acid receptor-ionophore complex. GABA-A receptors appear to have at least three allosteric sites at which modulators act: a site at which benzodiazepines act by increasing the opening frequency of gamma-aminobutyric acid-activated chloride channels; a site at which barbiturates act to prolong the duration of channel opening; and a site at which some steroids may act.
ChEBI Ontology
Outgoing Relation(s)
pinocarveol (CHEBI:26137) has role GABA modulator (CHEBI:50268)
pinocarveol (CHEBI:26137) has role mouse metabolite (CHEBI:75771)
pinocarveol (CHEBI:26137) has role plant metabolite (CHEBI:76924)
pinocarveol (CHEBI:26137) has role volatile oil component (CHEBI:27311)
pinocarveol (CHEBI:26137) is a carbobicyclic compound (CHEBI:36785)
pinocarveol (CHEBI:26137) is a pinane monoterpenoid (CHEBI:26133)
pinocarveol (CHEBI:26137) is a secondary alcohol (CHEBI:35681)
Incoming Relation(s)
(−)-trans-pinocarveol (CHEBI:83263) is a pinocarveol (CHEBI:26137)
IUPAC Name 
6,6-dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol
Synonyms  Source
6,6-Dimethyl-2-methylenebicyclo(3.1.1)heptan-3-olChemIDplus
10-Pinen-3-olChemIDplus
2(10)-Pinen-3-olChemIDplus
3-Hydroxy-6,6-dimethyl-2-methylenebicyclo(3.1.1)heptaneChemIDplus
Manual XrefsDatabases
c0629UM-BBD
C11941KEGG COMPOUND
LMPR0102120025LIPID MAPS
HMDB0035743HMDB
Registry NumbersSources
Reaxys:2042781Reaxys
CAS:5947-36-4KEGG COMPOUND
CAS:5947-36-4UM-BBD
CAS:5947-36-4NIST Chemistry WebBook
CAS:5947-36-4ChemIDplus
Citations