Page last updated: 2024-08-17

2,6-dihydroxyanthraquinone and 9,10-anthraquinone

2,6-dihydroxyanthraquinone has been researched along with 9,10-anthraquinone in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's3 (60.00)29.6817
2010's0 (0.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Hong, CY; Huang, SS; Yeh, SF1
Strassburg, CP; Tukey, RH1
Matsuda, H; Morikawa, T; Shimoda, H; Yoshikawa, M1
Kobayashi, N; Koyama, J; Morita, I; Nisino, Y; Osakai, T; Tokuda, H1
Lefin, R; Petzer, A; Petzer, JP1

Reviews

1 review(s) available for 2,6-dihydroxyanthraquinone and 9,10-anthraquinone

ArticleYear
Human UDP-glucuronosyltransferases: metabolism, expression, and disease.
    Annual review of pharmacology and toxicology, 2000, Volume: 40

    Topics: Autoimmunity; Chromosome Mapping; Glucuronides; Glucuronosyltransferase; Humans; Hyperbilirubinemia; Neoplasms; Steroids; Terminology as Topic

2000

Other Studies

4 other study(ies) available for 2,6-dihydroxyanthraquinone and 9,10-anthraquinone

ArticleYear
Effect of anthraquinone derivatives on lipid peroxidation in rat heart mitochondria: structure-activity relationship.
    Journal of natural products, 1995, Volume: 58, Issue:9

    Topics: Animals; Anthraquinones; Antioxidants; Free Radical Scavengers; In Vitro Techniques; Lipid Peroxidation; Male; Mitochondria, Heart; Rats; Rats, Sprague-Dawley; Structure-Activity Relationship

1995
Phytoestrogens from the roots of Polygonum cuspidatum (Polygonaceae): structure-requirement of hydroxyanthraquinones for estrogenic activity.
    Bioorganic & medicinal chemistry letters, 2001, Jul-23, Volume: 11, Issue:14

    Topics: Anthraquinones; Cell Division; Cells, Cultured; Emodin; Estradiol; Estrogen Receptor alpha; Estrogen Receptor beta; Estrogens, Non-Steroidal; Genistein; Humans; Isoflavones; Phytoestrogens; Plant Preparations; Polygonaceae; Protein Binding; Receptors, Estrogen; Structure-Activity Relationship

2001
Correlation between reduction potentials and inhibitions of Epstein-Barr virus activation by anthraquinone derivatives.
    Bioorganic & medicinal chemistry letters, 2008, Jul-15, Volume: 18, Issue:14

    Topics: Anthraquinones; Antiviral Agents; Buffers; Cell Line, Tumor; Chemistry, Pharmaceutical; Drug Design; Emodin; Herpesvirus 4, Human; Humans; Hydrogen-Ion Concentration; Inhibitory Concentration 50; Methylation; Models, Chemical; Virus Activation

2008
Phenothiazine, anthraquinone and related tricyclic derivatives as inhibitors of monoamine oxidase.
    Bioorganic & medicinal chemistry, 2022, 01-15, Volume: 54

    Topics: Anthraquinones; Dose-Response Relationship, Drug; Humans; Molecular Structure; Monoamine Oxidase; Monoamine Oxidase Inhibitors; Phenothiazines; Structure-Activity Relationship

2022