Substance | Relationship Strength | Studies | Trials | Classes | Roles |
camphor, (+-)-isomer [no description available] | 3.92 | 3 | 0 | bornane monoterpenoid; cyclic monoterpene ketone | plant metabolite |
eucalyptol [no description available] | 2.05 | 1 | 0 | | |
boranes Boranes: The collective name for the boron hydrides, which are analogous to the alkanes and silanes. Numerous boranes are known. Some have high calorific values and are used in high-energy fuels. (From Grant & Hackh's Chemical Dictionary, 5th ed). borane : The simplest borane, consisting of a single boron atom carrying three hydrogens.. boranes : The molecular hydrides of boron. | 2.05 | 1 | 0 | boranes; mononuclear parent hydride | |
cyclohexanol Cyclohexanols: Monohydroxy derivatives of cyclohexanes that contain the general formula R-C6H11O. They have a camphorlike odor and are used in making soaps, insecticides, germicides, dry cleaning, and plasticizers.. cyclohexanols : An alcohol in which one or more hydroxy groups are attached to a cyclohexane skeleton. | 2.05 | 1 | 0 | cyclohexanols; secondary alcohol | solvent |
beta-thujone [no description available] | 4.32 | 5 | 0 | beta-thujone | |
chrysanthenyl acetate chrysanthenyl acetate: structure given in first source | 2.05 | 1 | 0 | | |
chrysanthenone chrysanthenone: in oil of leaves of the Ethiopian plant Laggera tomentosa (Asteraceae); used in perfumery & toothpaste; structure in first source | 2.05 | 1 | 0 | monoterpenoid | |
davanone davanone: antifungal and antispasmodic isolated from natural Davana oil and Artemisia pallens; structure in first source | 2.05 | 1 | 0 | oxolanes | |
sesquiterpenes [no description available] | 2.49 | 2 | 0 | | |
isoborneol isoborneol: RN given refers to cpd without isomeric designation; structure | 2.05 | 1 | 0 | borneol | |
carbocysteine sabinol: RN given refers to (1S-(1alpha,3beta,5alpha))isomer; structure given in first source | 2.53 | 2 | 0 | | |