CHEBI:26137 - pinocarveol

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name pinocarveol
ChEBI ID CHEBI:26137
Definition A 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.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:29666
Supplier Information
Download Molfile XML SDF
Formula C10H16O
Net Charge 0
Average Mass 152.23344
Monoisotopic Mass 152.12012
InChI InChI=1S/C10H16O/c1-6-8-4-7(5-9(6)11)10(8,2)3/h7-9,11H,1,4-5H2,2-3H3
InChIKey LCYXQUJDODZYIJ-UHFFFAOYSA-N
SMILES CC1(C)C2CC(O)C(=C)C1C2
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Zingiber officinale (NCBI:txid94328) See: PubMed
Roles Classification
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
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.
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.
Application(s): 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.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 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 (−)-trans-pinocarveol (CHEBI:83263) is a pinocarveol (CHEBI:26137)
IUPAC Name
6,6-dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol
Synonyms Sources
10-Pinen-3-ol ChemIDplus
2(10)-Pinen-3-ol ChemIDplus
3-Hydroxy-6,6-dimethyl-2-methylenebicyclo(3.1.1)heptane ChemIDplus
6,6-Dimethyl-2-methylenebicyclo(3.1.1)heptan-3-ol ChemIDplus
Manual Xrefs Databases
c0629 UM-BBD
C11941 KEGG COMPOUND
HMDB0035743 HMDB
LMPR0102120025 LIPID MAPS
View more database links
Registry Numbers Types Sources
2042781 Reaxys Registry Number Reaxys
5947-36-4 CAS Registry Number KEGG COMPOUND
5947-36-4 CAS Registry Number UM-BBD
5947-36-4 CAS Registry Number ChemIDplus
5947-36-4 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations Types Sources
20590154 PubMed citation Europe PMC
24273211 PubMed citation Europe PMC
24455984 PubMed citation Europe PMC
Last Modified
27 January 2016