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tetrahydroxyflavone

Any hydroxyflavone carrying four hydroxy substituents.

ChEBI ID: 38684

Members (31)

MemberDefinitionRole
3-methylquercetinA monomethoxyflavone that is quercetin in which the hydroxy group at position 3' is replaced by a methoxy group.isorhamnetin
avicularinA quercetin O-glycoside in which an alpha-L-arabinofuranosyl residue is attached at position 3 of quercetin via a glycosidic linkage. It is isolated particularly from Juglans regia and Foeniculum vulgare.avicularin
axillarinA dimethoxyflavone that is the 3,6-dimethyl ether derivative of quercetagetin.axillarin
azaleatinA monomethoxyflavone that is quercetin in which the hydroxy group at position 5 is replaced by a methoxy group.azaleatin
cudraflavone cA tetrahydroxyflavone that is flavone substituted by hydroxy groups at positions 5, 7, 2' and 4' and prenyl groups at positions 3 and 6. Isolated from Morus nigra, it exhibits antibacterial and cytotoxic activities.cudraflavone C
datiscetinA tetrahydroxyflavone that is 7-hydroxyflavonol bearing two additional hydroxy substituents at positions 2' and 5.datiscetin
fisetinA 7-hydroxyflavonol with additional hydroxy groups at positions 3, 3' and 4'.fisetin
homoorientinA flavone C-glycoside consisting of luteolin having a beta-D-glucosyl residue at the 6-position.isoorientin
hyperosideA quercetin O-glycoside that is quercetin with a beta-D-galactosyl residue attached at position 3. Isolated from Artemisia capillaris, it exhibits hepatoprotective activity.quercetin 3-O-beta-D-galactopyranoside
isoscutellareinA tetrahydroxyflavone that is apigenin with an extra hydroxy group at position 8.isoscutellarein
kaempferolA tetrahydroxyflavone in which the four hydroxy groups are located at positions 3, 5, 7 and 4'. Acting as an antioxidant by reducing oxidative stress, it is currently under consideration as a possible cancer treatment.kaempferol
kuwanon gA tetrahydroxyflavone isolated from the root barks of Morus alba and has been shown to exhibit anti-inflammatory activity.kuwanone G
kuwanon hA tetrahydroxyflavone isolated from the plant species of the genus Morus.kuwanone H
luteolinA tetrahydroxyflavone in which the four hydroxy groups are located at positions 3', 4', 5 and 7. It is thought to play an important role in the human body as an antioxidant, a free radical scavenger, an anti-inflammatory agent and an immune system modulator as well as being active against several cancers.luteolin
maysinA flavone C-glycoside that is luteolin attached to a disaccharide residue at position 6. It has been isolated from natural product Petrorhagia velutina and Zea mays and exhibits insecticidal and neuroprotective activities.maysin
orientinA C-glycosyl compound that is luteolin substituted by a beta-D-glucopyranosyl moiety at position 8.orientin
pedalitinA tetrahydroxy-monohydroxy-flavone, with the four hydroxy groups at C-3',-4',-5 and 6, and the methoxy group at C-7. It has been isolated from a number of plant species, including Eremosparton songoricum, Rabdosia japonica and Ruellia tuberosa.pedalitin
quercetin 3-o-gentiobiosideA quercetin O-glycoside in which the hydroxy hydrogen at position 3 of quercetin has been replaced by a gentiobiosyl group.quercetin 3-beta-gentiobioside
quercetin 3-o-glucopyranosideA quercetin O-glucoside that is quercetin with a beta-D-glucosyl residue attached at position 3. Isolated from Lepisorus contortus, it exhibits antineoplastic activityand has been found to decrease the rate of polymerization and sickling of red blood cellsquercetin 3-O-beta-D-glucopyranoside
quercetin 3-o-methyl etherA tetrahydroxyflavone having the 4-hydroxy groups located at the 3'- 4'- 5- and 7-positions as well as a methoxy group at the 2-position.3',4',5,7-tetrahydroxy-3-methoxyflavone
quercetin 3-sambubiosideA quercetin O-glucoside that is quercetin attached to a beta-D-sambubiosyl residue at position 3 via a glycosidc linkage.2)-beta-D-glucoside].html>quercetin 3-O-[beta-D-xylosyl-(1->2)-beta-D-glucoside]
quercetin 7-rhamnosideA quercetin O-glycoside that is quercetin attached to a alpha-L-rhamnopyranosyl moiety at position 7 via a glycosidic linkage.quercetin 7-O-alpha-L-rhamnopyranoside
quercetin-3-o-sophorosideA quercetin O-glucoside that is quercetin attached to a beta-D-sophorosyl residue at position 3 via a glycosidic linkage.2)-beta-D-glucoside.html>quercetin 3-O-beta-D-glucosyl-(1->2)-beta-D-glucoside
quercimeritrinA quercetin O-glucoside in which a glucosyl residue is attached at position 7 of quercetin via a beta-glycosidic linkage.quercetin 7-O-beta-D-glucoside
quercitrinA quercetin O-glycoside that is quercetin substituted by a alpha-L-rhamnosyl moiety at position 3 via a glycosidic linkage.quercitrin
rhamnetinA monomethoxyflavone that is quercetin methylated at position 7.rhamnetin
rutinA rutinoside that is quercetin with the hydroxy group at position C-3 substituted with glucose and rhamnose sugar groups.rutin
scutellareinFlavone substituted with hydroxy groups at C-4', -5, -6 and -7.scutellarein
spiraeosideA quercetin O-glucoside that is quercetin with a beta-D-glucosyl residue attached at position 4'.quercetin 4'-O-beta-D-glucopyranoside
syringetinA dimethoxyflavone that is myricetin in which the hydroxy groups at positions 3' and 5' have been replaced by methoxy groups.syringetin
tamarixetinA monomethoxyflavone that is quercetin methylated at position O-4'. Isolated from Cyperus teneriffae.tamarixetin

Research

Studies (9,254)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-19901,165 (12.59)18.7374
1990's437 (4.72)18.2507
2000's1,852 (20.01)29.6817
2010's4,073 (44.01)24.3611
2020's1,727 (18.66)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials300 (2.74%)5.53%
Reviews390 (3.57%)6.00%
Case Studies37 (0.34%)4.05%
Observational4 (0.04%)0.25%
Other10,202 (93.31%)84.16%