Compounds > chrysanthenone
Page last updated: 2024-12-08

chrysanthenone

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

chrysanthenone: in oil of leaves of the Ethiopian plant Laggera tomentosa (Asteraceae); used in perfumery & toothpaste; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

FloraRankFlora DefinitionFamilyFamily Definition
Laggeragenus[no description available]AsteraceaeA large plant family of the order Asterales, subclass Asteridae, class Magnoliopsida. The family is also known as Compositae. Flower petals are joined near the base and stamens alternate with the corolla lobes. The common name of daisy refers to several genera of this family including Aster; CHRYSANTHEMUM; RUDBECKIA; TANACETUM.[MeSH]
Laggera tomentosaspecies[no description available]AsteraceaeA large plant family of the order Asterales, subclass Asteridae, class Magnoliopsida. The family is also known as Compositae. Flower petals are joined near the base and stamens alternate with the corolla lobes. The common name of daisy refers to several genera of this family including Aster; CHRYSANTHEMUM; RUDBECKIA; TANACETUM.[MeSH]

Cross-References

ID SourceID
PubMed CID442463
CHEBI ID19
CHEBI ID3681
SCHEMBL ID2384039
MeSH IDM0408200

Synonyms (12)

Synonym
bicyclo[3.1.1]hept-2-en-6-one, 2,7,7-trimethyl-
chrysanthenone
C09843
AC1L9CVQ ,
CHEBI:19
CHEBI:3681
SCHEMBL2384039
2,7,7-trimethylbicyclo[3.1.1]hept-2-en-6-one #
IECBDTGWSQNQID-UHFFFAOYSA-N
2,7,7-trimethylbicyclo[3.1.1]hept-2-en-6-one
DTXSID80894868
Q5114549
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
monoterpenoidAny terpenoid derived from a monoterpene. The term includes compounds in which the C10 skeleton of the parent monoterpene has been rearranged or modified by the removal of one or more skeletal atoms (generally methyl groups).
monoterpenoidAny terpenoid derived from a monoterpene. The term includes compounds in which the C10 skeleton of the parent monoterpene has been rearranged or modified by the removal of one or more skeletal atoms (generally methyl groups).
[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]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (60.00)29.6817
2010's1 (20.00)24.3611
2020's1 (20.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 24.51

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index24.51 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.66 (4.65)
Search Engine Demand Index23.28 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (24.51)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
camphor, (+-)-isomer
[no description available]		2.7830bornane monoterpenoid;
cyclic monoterpene ketone		plant metabolite
eucalyptol
[no description available]		2.4520
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.		2.9640boranes;
mononuclear parent hydride
camphene
camphene : A monoterpene with a bicyclic skeleton that is bicyclo[2.2.1]heptane substituted by geminal methyl groups at position 2 and a methylidene group at position 3. It is a widespread natural product found in many essential oils.		2.0410carbobicyclic compound;
monoterpene		fragrance;
plant metabolite
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.		2.4520cyclohexanols;
secondary alcohol		solvent
beta-selinene
beta-selinene: isolated from aerial parts of Ligusticum chuanxiong; RN given for (4aR-(4aalpha,7alpha,8abeta))-isomer. (-)-beta-selinene : The (4aS,7S,8aR)-stereoisomer of beta-selinene.		2.0410beta-selinene
beta-thujone
[no description available]		2.5320beta-thujone
sabinyl acetate
sabinyl acetate: present in essential oils; RN given refers to cpd without isomeric designation		2.0510
chrysanthenyl acetate
chrysanthenyl acetate: structure given in first source		2.0510
davanone
davanone: antifungal and antispasmodic isolated from natural Davana oil and Artemisia pallens; structure in first source		2.0510oxolanes
sesquiterpenes
[no description available]		2.4520
caryophyllene oxide
caryophyllene oxide: has butyrylcholinesterase inhibitory activity; structure in first source. epoxide : Any cyclic ether in which the oxygen atom forms part of a 3-membered ring.		2.0410epoxidemetabolite
bornyl acetate
[no description available]		2.0410acetate ester;
monoterpenoid
isoborneol
isoborneol: RN given refers to cpd without isomeric designation; structure		2.7830borneol
ConditionIndicatedRelationship StrengthStudiesTrials