(-)-trans-pinocarveol (CHEBI:83263)

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ChEBI Name	*(−)-trans-pinocarveol*

ChEBI ID	CHEBI:83263

ChEBI ASCII Name	(-)-trans-pinocarveol

Definition	The (1S,3R,5S)-stereoisomer of pinocarveol.

Stars	This entity has been manually annotated by the ChEBI Team.

Supplier Information

Download	Molfile XML SDF

Formula

C10H16O

Net Charge

Average Mass

152.23340

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/t7-,8+,9+/m0/s1

InChIKey

LCYXQUJDODZYIJ-DJLDLDEBSA-N

SMILES

CC1(C)[C@H]2C[C@@H]1C(=C)[C@H](O)C2

Metabolite of Species	Details
Eucalyptus perriniana (NCBI:txid183845)	See: PubMed

Roles Classification
Biological Role(s):	mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). (via pinocarveol ) 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. (via pinocarveol ) plant metabolite Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms. (via pinocarveol ) volatile oil component Any plant metabolite that is found naturally as a component of a volatile oil. (via pinocarveol )

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. (via pinocarveol )

ChEBI Ontology
Outgoing	(−)-trans-pinocarveol (CHEBI:83263) is a pinocarveol (CHEBI:26137)

IUPAC Name

(1S,3R,5S)-6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptan-3-ol

Last Modified

10 October 2014