cubebol: antifeedants against Acusta despesta from the Japanese cedar, Cryptomeria japonica II; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
(-)-cubebol : A tertiary alcohol resulting from the formal addition of water to the double bond of alpha-cubebene. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]
| Flora | Rank | Flora Definition | Family | Family Definition |
|---|---|---|---|---|
| Cryptomeria | genus | A plant genus of the family CUPRESSACEAE which produce POLLEN that is a major ALLERGEN.[MeSH] | Cupressaceae | A plant family of the order Pinales, class Pinopsida, division Tracheophyta. They are mainly resinous, aromatic evergreen trees.[MeSH] |
| Cryptomeria japonica | species | [no description available] | Cupressaceae | A plant family of the order Pinales, class Pinopsida, division Tracheophyta. They are mainly resinous, aromatic evergreen trees.[MeSH] |
| ID Source | ID |
|---|---|
| PubMed CID | 11276107 |
| CHEBI ID | 63446 |
| SCHEMBL ID | 246610 |
| MeSH ID | M0408533 |
| Synonym |
|---|
| (-)-(1r,4s,5r,6r,7s,10r)-7-isopropyl-4,10-dimethyl-tricyclo[4.4.0.0(1,5)]decan-4-ol |
| (3s,3ar,3br,4s,7r,7ar)-3,7-dimethyl-4-(propan-2-yl)octahydro-1h-cyclopenta[1,3]cyclopropa[1,2]benzen-3-ol |
| (-)-cubebol |
| 23445-02-5 |
| cubeb camphor |
| CHEBI:63446 |
| cubebol |
| (1r,4s,5r,6r,7s,10r)-7-isopropyl-4,10-dimethyl-tricyclo[4.4.0.0(1,5)]decan-4-ol |
| 1h-cyclopenta(1,3)cyclopropa(1,2)benzen-3-ol, octahydro-3,7-dimethyl-4-(1-methylethyl)-, (3s-(3alpha,3abeta,3balpha,4alpha,7beta,7as*))- |
| 1h-cyclopenta(1,3)cyclopropa(1,2)benzen-3-ol, octahydro-3,7-dimethyl-4-(1-methylethyl)-, (3s,3ar,3br,4s,7r,7ar)- |
| 1h-cyclopenta(1,3)cyclopropa(1,2)benzen-3-ol, 2,3,3aalpha,3balpha,4,5,6,7-octahydro-4alpha-isopropyl-3beta,7betadimethyl-, (-)- |
| unii-9c9zts2b3u |
| fema no. 4497 |
| 9c9zts2b3u , |
| 1h-cyclopenta(1,3)cyclopropa(1,2)benzen-3-ol, 2,3,3a.alpha.,3b.alpha.,4,5,6,7-octahydro-4.alpha.-isopropyl-3.beta.,7.beta-dimethyl-, (-)- |
| 1h-cyclopenta(1,3)cyclopropa(1,2)benzen-3-ol, octahydro-3,7-dimethyl-4-(1-methylethyl)-, (3s-(3.alpha.,3a.beta.,3b.alpha.,4.alpha.,7.beta.,7as*))- |
| SCHEMBL246610 |
| DTXSID90177997 |
| Q726875 |
| (1r,4s,5r,6r,7s,10r)-4,10-dimethyl-7-isopropyltricyclo[4.4.0.01,5]decane-4-ol |
| (1r,4s,5r,6r,7s,10r)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]decan-4-ol |
| Class | Description |
|---|---|
| sesquiterpenoid | Any terpenoid derived from a sesquiterpene. The term includes compounds in which the C15 skeleton of the parent sesquiterpene has been rearranged or modified by the removal of one or more skeletal atoms (generally methyl groups). |
| tertiary alcohol | A tertiary alcohol is a compound in which a hydroxy group, -OH, is attached to a saturated carbon atom which has three other carbon atoms attached to it. |
| carbotricyclic compound | A carbopolyclic compound comprising of three carbocyclic rings. |
| [compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] | |
| Timeframe | Studies, This Drug (%) | All Drugs % |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (37.50) | 29.6817 |
| 2010's | 3 (37.50) | 24.3611 |
| 2020's | 2 (25.00) | 2.80 |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||
| Publication Type | This drug (%) | All Drugs (%) |
|---|---|---|
| Trials | 0 (0.00%) | 5.53% |
| Reviews | 0 (0.00%) | 6.00% |
| Case Studies | 0 (0.00%) | 4.05% |
| Observational | 0 (0.00%) | 0.25% |
| Other | 8 (100.00%) | 84.16% |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||