Page last updated: 2024-11-13

cycloeucalenone

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

Description

cycloeucalenone: from the stems of Tinospora crispa; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

cycloeucalenone : A pentacyclic triterpenoid that is 4alpha,14-dimethyl-9beta,19-cyclo-5alpha-ergost-24(28)-ene which is substituted by an oxo group at position 3. It has been isolated from several plant species including Quercus variabilis, Ammocharis coranica, Solanum cernuum and Tinospora crispa. [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]

FloraRankFlora DefinitionFamilyFamily Definition
SolanumgenusA plant genus of the family SOLANACEAE. Members contain SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for ATROPA BELLADONNA.[MeSH]SolanaceaeA plant family of the order SOLANALES, class MAGNOLIOPSIDA. Among the most noted are POTATOES; TOMATOES; CAPSICUM (green and red peppers); TOBACCO; and BELLADONNA.[MeSH]
Ammocharisgenus[no description available]AmaryllidaceaeA family of herbaceous plants with bulbs or rhizomes in the order Asparagales.[MeSH]
QuercusgenusA plant genus of the family FAGACEAE that is a source of TANNINS. Do not confuse with Holly (ILEX).[MeSH]FagaceaeA plant family of the order Fagales subclass Hamamelidae, class Magnoliopsida.[MeSH]
TinosporagenusA plant genus of the family MENISPERMACEAE. Members have been used in AYURVEDIC MEDICINE. Hypoglycemic effect has been reported.[MeSH]MenispermaceaeA plant family of the order Ranunculales, subclass Magnoliidae, class Magnoliopsida. Members are mostly vines and shrubs and they contain isoquinoline alkaloids, some of which have been used as arrow poisons.[MeSH]
Solanum cernuumspecies[no description available]SolanaceaeA plant family of the order SOLANALES, class MAGNOLIOPSIDA. Among the most noted are POTATOES; TOMATOES; CAPSICUM (green and red peppers); TOBACCO; and BELLADONNA.[MeSH]
Ammocharis coranicaspecies[no description available]AmaryllidaceaeA family of herbaceous plants with bulbs or rhizomes in the order Asparagales.[MeSH]
Quercus variabilisspecies[no description available]FagaceaeA plant family of the order Fagales subclass Hamamelidae, class Magnoliopsida.[MeSH]

Cross-References

ID SourceID
PubMed CID21594790
CHEMBL ID225754
CHEBI ID142915
MeSH IDM0447603

Synonyms (11)

Synonym
CHEMBL225754
4alpha,14-dimethyl-9beta,19-cyclo-5alpha-ergost-24(28)-en-3-one
CHEBI:142915
1255-12-5
(4alpha,5alpha,9beta)-4,14-dimethyl-9,19-cycloergost-24(28)-en-3-one
cycloeucalenone
4alpha,14alpha-dimethyl-9beta,19-cyclo-ergost-24(241)-en-3-one
9,19-cyclo-5alpha,9beta-ergost-24(28)-en-3-one
3h,19h-cyclopropa[9,10]cyclopenta[a]phenanthrene
C22121
(1s,3r,7s,8s,11s,12s,15r,16r)-7,12,16-trimethyl-15-[(2r)-6-methyl-5-methylideneheptan-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
[role 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]

Drug Classes (3)

ClassDescription
3-oxo-5alpha-steroidA 3-oxo steroid that has alpha configuration at position 5.
pentacyclic triterpenoid
cyclic terpene ketoneAn alicyclic ketone in which the carbocyclic ring structure forms part of a terpene skeleton.
[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]

Bioassays (7)

Assay IDTitleYearJournalArticle
AID288763Inhibition of TPA-induced Epstein-Barr virus early antigen activation assessed as EBV-EA induction in Raji cells at 0.32 nM after 48 hrs relative to TPA2007Journal of natural products, Jun, Volume: 70, Issue:6
Cancer chemopreventive effects of cycloartane-type and related triterpenoids in in vitro and in vivo models.
AID288764Inhibition of TPA-induced Epstein-Barr virus early antigen activation in Raji cells after 48 hrs2007Journal of natural products, Jun, Volume: 70, Issue:6
Cancer chemopreventive effects of cycloartane-type and related triterpenoids in in vitro and in vivo models.
AID288766Scavenging activity against NO generation in human Chang liver cells assessed as inhibition of NOR1-activation at 350 nM relative to NOR12007Journal of natural products, Jun, Volume: 70, Issue:6
Cancer chemopreventive effects of cycloartane-type and related triterpenoids in in vitro and in vivo models.
AID288760Inhibition of TPA-induced Epstein-Barr virus early antigen activation assessed as EBV-EA induction in Raji cells at 320 nM after 48 hrs relative to TPA2007Journal of natural products, Jun, Volume: 70, Issue:6
Cancer chemopreventive effects of cycloartane-type and related triterpenoids in in vitro and in vivo models.
AID288765Cell viability of Raji cells at 320 nM2007Journal of natural products, Jun, Volume: 70, Issue:6
Cancer chemopreventive effects of cycloartane-type and related triterpenoids in in vitro and in vivo models.
AID288761Inhibition of TPA-induced Epstein-Barr virus early antigen activation assessed as EBV-EA induction in Raji cells at 32 nM after 48 hrs relative to TPA2007Journal of natural products, Jun, Volume: 70, Issue:6
Cancer chemopreventive effects of cycloartane-type and related triterpenoids in in vitro and in vivo models.
AID288762Inhibition of TPA-induced Epstein-Barr virus early antigen activation assessed as EBV-EA induction in Raji cells at 3.2 nM after 48 hrs relative to TPA2007Journal of natural products, Jun, Volume: 70, Issue:6
Cancer chemopreventive effects of cycloartane-type and related triterpenoids in in vitro and in vivo models.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (4)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 23.30

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 Index23.30 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.51 (4.65)
Search Engine Demand Index21.17 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (23.30)

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]