Page last updated: 2024-12-11

artemetin

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

Cross-References

ID SourceID
PubMed CID5320351
CHEMBL ID225700
CHEBI ID175930
SCHEMBL ID2122576
MeSH IDM0153038

Synonyms (40)

Synonym
CHEBI:175930
2-(3,4-dimethoxyphenyl)-5-hydroxy-3,6,7-trimethoxychromen-4-one
479-90-3
ACON1_000985
MEGXP0_002022
artemisetin
2-(3,4-dimethoxyphenyl)-5-hydroxy-3,6,7-trimethoxy-chromen-4-one
5'-hydroxy-3,3',4',6,7-pentamethoxyflavone
4h-1-benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5-hydroxy-3,6,7-trimethoxy-
NCGC00169786-01
CHEMBL225700
BRD-K39946608-001-01-8
artemetin
LMPK12113017
quercetagetin 3,6,7,3',4'-pentamethyl ether
unii-73kmt7r64h
5-hydroxy-3,3',4',6,7-pentamethoxyflavone
73kmt7r64h ,
SCHEMBL2122576
5-hydroxy-3,3',4',6,7-pentamethoxy-flavone
3,6,7,3',4'-pentamethylquercetagetin
AC-34968
2-(3,4-dimethoxyphenyl)-5-hydroxy-3,6,7-trimethoxy-4h-chromen-4-one #
erianthin
RIGYMJVFEJNCKD-UHFFFAOYSA-N
flavone, 5-hydroxy-3,3',4',6,7-pentamethoxy-
5-hydroxy-3,6,7,3',4'-pentamethoxyflavone
DTXSID20197325
artemisetin(p)
artemitin
quercetagetin-3,6,7,3',4'-pentamethylether
penta-o-methylquercetagetin
AKOS032948424
2-(3,4-dimethoxyphenyl)-5-hydroxy-3,6,7-trimethoxy-4h-chromen-4-one
HY-N3017
CS-0022980
FT-0777586
Q27266189
MS-26430
A871998

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
" A marked cell bioavailability increase was demonstrated for the artemetin C-prenylated derivative."( Effects of quercetin and artemetin prenylation on bioavailability and bioactivity.
Bombardelli, E; Khalili, A; Nieddu, M; Pollastro, F; Rosa, A; Salamone, S; Sansaro, A, 2021
)
1.16
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
flavonoidsAny organic molecular entity whose stucture is based on derivatives of a phenyl-substituted 1-phenylpropane possessing a C15 or C16 skeleton, or such a structure which is condensed with a C6-C3 lignan precursors. The term is a 'superclass' comprising all members of the classes of flavonoid, isoflavonoid, neoflavonoid, chalcones, dihydrochalcones, aurones, pterocarpan, coumestans, rotenoid, flavonolignan, homoflavonoid and flavonoid oligomers. Originally restricted to natural products, the term is also applied to synthetic compounds related to them.
etherAn organooxygen compound with formula ROR, where R is not hydrogen.
[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]

Pathways (2)

PathwayProteinsCompounds
polymethylated quercetin glucoside biosynthesis II - quercetagetin series (Chrysosplenium)231
superpathway of polymethylated quercetin/quercetagetin glucoside biosynthesis (Chrysosplenium)234
polymethylated quercetin glucoside biosynthesis II - quercetagetin series (Chrysosplenium)238
superpathway of polymethylated quercetin/quercetagetin glucoside biosynthesis (Chrysosplenium)246

Bioassays (27)

Assay IDTitleYearJournalArticle
AID663321Antiinflammatory activity in human neutrophils assessed as inhibition of FMLP/CB-induced elastase release using Meo-Suc-Ala-Ala-Pro-Val-p-nitroanilide as substrate incubated for 5 mins prior to FMLP/CB-challenge by spectrophotometry2012Journal of natural products, Apr-27, Volume: 75, Issue:4
Bioactive diterpenes from Callicarpa longissima.
AID304975Antifungal activity against Trichophyton mentagrophytes by broth micro-dilution technique2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
New antifungal flavonoid glycoside from Vitex negundo.
AID1546567Cytotoxicity against human HepG2 cells after 72 hrs by MTT assay2020Bioorganic & medicinal chemistry, 01-01, Volume: 28, Issue:1
Artemisia: a promising plant for the treatment of cancer.
AID288087Apoptotic activity in HL60 cells after 24 hrs2007Bioorganic & medicinal chemistry, May-15, Volume: 15, Issue:10
Isolation and syntheses of polymethoxyflavones and hydroxylated polymethoxyflavones as inhibitors of HL-60 cell lines.
AID379312Antioxidant scavenging activity against 2,2'-azobis-amidinopropane-induced peroxyl radicals assessed as total oxyradical scavenging capacity relative to Trolox2000Journal of natural products, Mar, Volume: 63, Issue:3
Evaluation of the total peroxyl radical-scavenging capacity of flavonoids: structure-activity relationships.
AID304977Antifungal activity against Candida parapsilosis ATCC 22019 by broth micro-dilution technique2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
New antifungal flavonoid glycoside from Vitex negundo.
AID1242377Positive inotropic effect in Sprague-Dawley rat ventricular myocytes assessed as change in ventricular cell contractility at 10 uM by video edge detector relative to control2015ACS medicinal chemistry letters, Jul-09, Volume: 6, Issue:7
Exploration of Pharmacophore in Chrysosplenol C as Activator in Ventricular Myocyte Contraction.
AID334225Cytotoxicity against human HCT116 cells assessed as growth inhibition after 72 hrs by MTT assay2002Journal of natural products, Apr, Volume: 65, Issue:4
New diterpenes and norditerpenes from the fruits of Vitex rotundifolia.
AID663320Antiinflammatory activity in human neutrophils assessed as inhibition of FMLP/CB-induced superoxide-anion generation incubated for 5 mins prior to FMLP/CB-challenge measured after 10 mins by spectrophotometry2012Journal of natural products, Apr-27, Volume: 75, Issue:4
Bioactive diterpenes from Callicarpa longissima.
AID334224Cytotoxicity against rat PC12 cells assessed as growth inhibition after 72 hrs by MTT assay2002Journal of natural products, Apr, Volume: 65, Issue:4
New diterpenes and norditerpenes from the fruits of Vitex rotundifolia.
AID304971Antibacterial activity against Staphylococcus aureus by broth micro-dilution technique2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
New antifungal flavonoid glycoside from Vitex negundo.
AID1546568Cytotoxicity against human SH-SY5Y cells after 72 hrs by MTT assay2020Bioorganic & medicinal chemistry, 01-01, Volume: 28, Issue:1
Artemisia: a promising plant for the treatment of cancer.
AID304970Antibacterial activity against Pseudomonas aeruginosa by broth micro-dilution technique2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
New antifungal flavonoid glycoside from Vitex negundo.
AID304974Antifungal activity against Sporothrix schenckii by broth micro-dilution technique2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
New antifungal flavonoid glycoside from Vitex negundo.
AID379313Antioxidant scavenging activity against 2,2'-azobis-amidinopropane-induced peroxyl radicals assessed as total oxyradical scavenging capacity2000Journal of natural products, Mar, Volume: 63, Issue:3
Evaluation of the total peroxyl radical-scavenging capacity of flavonoids: structure-activity relationships.
AID304976Antifungal activity against Aspergillus fumigatus by broth micro-dilution technique2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
New antifungal flavonoid glycoside from Vitex negundo.
AID422404Antitubercular activity against Mycobacterium tuberculosis H37Rv after 2 weeks2009Journal of natural products, Feb-27, Volume: 72, Issue:2
seco-Abietane diterpenoids, a phenylethanoid derivative, and antitubercular constituents from Callicarpa pilosissima.
AID304973Antifungal activity against Cryptococcus neoformans by broth micro-dilution technique2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
New antifungal flavonoid glycoside from Vitex negundo.
AID288086Antiproliferative activity against HL60 after 24 hrs2007Bioorganic & medicinal chemistry, May-15, Volume: 15, Issue:10
Isolation and syntheses of polymethoxyflavones and hydroxylated polymethoxyflavones as inhibitors of HL-60 cell lines.
AID304972Antifungal activity against Candida albicans by broth micro-dilution technique2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
New antifungal flavonoid glycoside from Vitex negundo.
AID304968Antibacterial activity against Klebsiella pneumoniae by broth micro-dilution technique2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
New antifungal flavonoid glycoside from Vitex negundo.
AID1242378Positive inotropic effect in Sprague-Dawley rat ventricular myocytes assessed as change in ventricular cell contractility at 50 uM by video edge detector relative to control2015ACS medicinal chemistry letters, Jul-09, Volume: 6, Issue:7
Exploration of Pharmacophore in Chrysosplenol C as Activator in Ventricular Myocyte Contraction.
AID288088Cytotoxicity against human PMN cells at 100 uM2007Bioorganic & medicinal chemistry, May-15, Volume: 15, Issue:10
Isolation and syntheses of polymethoxyflavones and hydroxylated polymethoxyflavones as inhibitors of HL-60 cell lines.
AID629056Agonist activity at full length mouse FXR/RXRalpha expressed in human HEK293 cells assessed as induction of transcriptional activity at 10 ug/mL after 18 hrs by dual luciferase reporter gene assay relative to control2011Bioorganic & medicinal chemistry, Nov-15, Volume: 19, Issue:22
Pharmacophore-based discovery of FXR-agonists. Part II: identification of bioactive triterpenes from Ganoderma lucidum.
AID1546569Cytotoxicity against mouse S17 cells after 72 hrs by MTT assay2020Bioorganic & medicinal chemistry, 01-01, Volume: 28, Issue:1
Artemisia: a promising plant for the treatment of cancer.
AID304967Antibacterial activity against Streptococcus faecalis by broth micro-dilution technique2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
New antifungal flavonoid glycoside from Vitex negundo.
AID304969Antibacterial activity against Escherichia coli by broth micro-dilution technique2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
New antifungal flavonoid glycoside from Vitex negundo.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (27)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (3.70)18.7374
1990's1 (3.70)18.2507
2000's10 (37.04)29.6817
2010's12 (44.44)24.3611
2020's3 (11.11)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 26.52

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 Index26.52 (24.57)
Research Supply Index3.33 (2.92)
Research Growth Index5.18 (4.65)
Search Engine Demand Index29.35 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (26.52)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (3.70%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other26 (96.30%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]