Page last updated: 2024-08-05 11:14:32

dihydroxyanthraquinone

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ChEBI ID: 37484

Members (17)

MemberDefinitionRole
1,4-dihydroxyanthraquinoneA dihydroxyanthraquinone having the two hydroxy substituents at the 1- and 4-positions; formally derived from anthraquinone by replacement of two hydrogen atoms by hydroxy groupsquinizarin
2,6-dihydroxyanthraquinoneA dihydroxyanthraquinone that is anthracene substituted by hydroxy groups at C-3 and C-7 and oxo groups at C-9 and C-10.anthraflavic acid
alizarinA dihydroxyanthraquinone that is anthracene-9,10-dione in which the two hydroxy groups are located at positions 1 and 2.alizarin
aloe emodinA dihydroxyanthraquinone that is chrysazin carrying a hydroxymethyl group at position 3. It has been isolated from plant species of the genus Aloe.Aloe emodin
anthraglycoside bEmodin 8-glucoside
anthrarufinA dihydroxyanthraquinone that is anthracene-9,10-dione substituted by hydroxy groups at positions 1 and 5.anthrarufin
chrysophanic acidA trihydroxyanthraquinone that is chrysazin with a methyl substituent at C-3. It has been isolated from Aloe vera and exhibits antiviral and anti-inflammatory activity.chrysophanol
danthronA dihydroxyanthraquinone that is anthracene-9,10-dione substituted by hydroxy groups at positions 1 and 8.chrysazin
knipholoneAn anthraquinone that is anthracene-9,10-dione substituted by hydroxy groups at positions 4 and 6, a methyl group at position 2 and a 3-acetyl-2,6-dihydroxy-4-methoxyphenyl group at position 1. It exhibits antioxidant, cytotoxic and antiplasmodial activities.knipholone
lucidinLucidin
mitoxantroneA dihydroxyanthraquinone that is 1,4-dihydroxy-9,10-anthraquinone which is substituted by 6-hydroxy-1,4-diazahexyl groups at positions 5 and 8.mitoxantrone
obtusifolinObtusifolin
physcioneA dihydroxyanthraquinone that is 9,10-anthraquinone bearing hydroxy substituents at positions 1 and 8, a methoxy group at position 3, and a methyl group at position 6. It has been widely isolated and characterised from both terrestrial and marine sources.physcion
questinA dihydroxyanthraquinone that is 1,6-dihyroxy-9,10-anthraquinone which is substituted by a methyl group at position 3 and a methoxy group at position 8.questin
rheinRhein
rubiadinA dihydroxyanthraquinone that is anthracene-9,10-dione substituted by hydroxy groups at positions 1 and 3 and a methyl group at position 2. It has been isolated from Rubia yunnanensis.rubiadin
soranjidiolA member of the class of hydroxyanthraquinones that is anthracene-9,10-dione substituted by hydroxy groups at positions 1 and 6 and a methyl group at position 2. It has been isolated from the roots of Rubia yunnanensis.1,6-dihydroxy-2-methyl-9,10-anthraquinone

Research

Studies (6,156)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-1990814 (13.22)18.7374
1990's1,331 (21.62)18.2507
2000's1,789 (29.06)29.6817
2010's1,707 (27.73)24.3611
2020's515 (8.37)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials1,055 (15.25%)5.53%
Reviews452 (6.53%)6.00%
Case Studies387 (5.59%)4.05%
Observational13 (0.19%)0.25%
Other5,011 (72.43%)84.16%