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hydroxyflavone

Any flavone in which one or more ring hydrogens are replaced by hydroxy groups.

ChEBI ID: 24698

Members (10)

MemberDefinitionRole
agathisflavoneA biflavonoid that is obtained by oxidative coupling of two molecules of apigenin resulting in a bond between positions C-6 and C-8 of the two chromene rings.agathisflavone
amentoflavoneA biflavonoid that is obtained by oxidative coupling of two molecules of apigenin resulting in a bond between positions C-3 of the hydroxyphenyl ring and C-8 of the chromene ring. A natural product found particularly in Ginkgo biloba and Hypericum perforatum.amentoflavone
cupressuflavoneA biflavonoid that is obtained by oxidative coupling of two molecules of apigenin resulting in a bond between positions C-8 of the two chromene rings respectively. Isolated from Cupressus sempervirens and Juniperus occidentalis, it exhibits free radical scavenging and antielastase activities.cupressuflavone
ginkgetinA biflavonoid that is the 7,4'-dimethyl ether derivative of amentoflavone. Isolated from Ginkgo biloba and Dioon, it exhibits anti-HSV-1, antineoplastic and inhibitory activities towards arachidonate 5-lipoxygenase and cyclooxygenase 2.ginkgetin
hinokiflavoneA biflavonoid that is apigenin substituted by a 4-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)phenoxy group at position 6. A diflavonyl ether, it is isolated from Rhus succedanea and has been found to possess significant cytotoxic potential.hinokiflavone
isochamaejasminA biflavonoid that consists of two units of 5,7,4'-trihydroxyflavanone joined together at position 3 and 3''.isochamaejasmin
morelloflavoneA biflavonoid found in Rheedia edulis and Garcinia livingstonei.(+)-morelloflavone
ochnaflavoneA biflavonoid with an ether linkage between the B-rings of the apigenin and luteolin subunits. It has been isolated from several members of the Ochnaceae plant family.ochnaflavone
robustaflavoneA biflavonoid that is obtained by oxidative coupling of two molecules of apigenin resulting in a bond between positions C-3 of the hydroxyphenyl ring and C-6 of the chromene ring. Isolated from Thuja orientalis and Rhus succedanea it exhibits antioxidant, cytotoxic and anti-hepatitis B activity.robustaflavone
sciadopitysinA biflavonoid that is a 7, 4', 4'''-trimethyl ether derivative of amentoflavone.sciadopitysin

Research

Studies (356)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-19908 (2.25)18.7374
1990's19 (5.34)18.2507
2000's69 (19.38)29.6817
2010's172 (48.31)24.3611
2020's88 (24.72)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews20 (4.60%)6.00%
Case Studies1 (0.23%)4.05%
Observational0 (0.00%)0.25%
Other414 (95.17%)84.16%