EMBL-EBI | Chemical Biology | ChEBI
Example searches: iron*, InChI=1S/CH4O/c1-2/h2H,1H3, caffeine | Advanced Search
CHEBI:83263 - (−)-trans-pinocarveol
| Formula | C10H16O |
| Net Charge | 0 |
| Average Mass | 152.237 |
| Monoisotopic Mass | 152.12012 |
| SMILES | C=C1[C@H](O)C[C@@H]2C[C@H]1C2(C)C |
| 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 |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Eucalyptus perriniana (ncbitaxon:183845) | - | PubMed (23980409) |
| 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) |
| (−)-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 |
| Synonyms | Source |
|---|---|
| (1S)-(-)-trans-Pinocarveol | HMDB |
| L-Pinocarveol | HMDB |
| trans-(-)-Pinocarveol | HMDB |
| L-trans-Pinocarveol | HMDB |
| Manual Xrefs | Databases |
|---|---|
| C00011040 | KNApSAcK |
| HMDB0036128 | HMDB |
| Registry Numbers | Sources |
|---|---|
| Reaxys:5730571 | Reaxys |
| CAS:1674-08-4 | ChemIDplus |
| Citations |
|---|