Page last updated: 2024-08-05 11:17:05

trihydroxyanthraquinone

A member of the class of hydroxyanthraquinones carrying three hydroxy substituents.

ChEBI ID: 37488

Members (10)

MemberDefinitionRole
1,3,6-trihydroxy-2-methyl-9,10-anthraquinoneA trihydroxyanthraquinone that is 9,10-anthraquinone substituted by hydroxy groups at positions 1, 3 and 6 and a methyl group at position 2. It has been isolated from the roots of Rubia yunnanensis.1,3,6-trihydroxy-2-methyl-9,10-anthraquinone
1,3,6-trihydroxy-8-n-propylanthraquinoneR1128A
1,3,8-trihydroxy-6-hydroxymethylanthraquinoneCitreorosein
4,5,7-trihydroxy-9,10-dioxo-2-anthracenecarboxylic acid4,5,7-trihydroxy-9,10-dioxo-2-anthracenecarboxylic acid
aurantio-obtusinA trihydroxyanthraquinone that is 1,3,7-trihydroxy-9,10-anthraquinone which is by methoxy groups at positions 2 and 8, and by a methyl group at position 6.aurantio-obtusin
emodinA trihydroxyanthraquinone that is 9,10-anthraquinone which is substituted by hydroxy groups at positions 1, 3, and 8 and by a methyl group at position 6. It is present in the roots and barks of numerous plants (particularly rhubarb and buckthorn), moulds, and lichens. It is an active ingredient of various Chinese herbs.emodin
endocrocinA trihydroxyanthraquinone that is 9,10-anthraquinone which is substituted by a carboxy group at position 2, a methyl group at position 3, and hydroxy groups at positions 1, 6, and 8.endocrocin
funiculosin (anthraquinone)Islandicin
purpurinA trihydroxyanthraquinone derived from anthracene by substitution with oxo groups at C-9 and C-10 and with hydroxy groups at C-1, C-2 and C-4.purpurin
skyrinskyrin

Research

Studies (1,855)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-199097 (5.23)18.7374
1990's111 (5.98)18.2507
2000's420 (22.64)29.6817
2010's808 (43.56)24.3611
2020's419 (22.59)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials3 (0.15%)5.53%
Reviews80 (4.07%)6.00%
Case Studies4 (0.20%)4.05%
Observational1 (0.05%)0.25%
Other1,876 (95.52%)84.16%