Compounds > 4',5-dihydroxy-3',6,7,8-tetramethoxyflavone
Page last updated: 2024-09-05

4',5-dihydroxy-3',6,7,8-tetramethoxyflavone and 4'-hydroxy-5,6,7,8,3'-pentamethoxyflavone

4',5-dihydroxy-3',6,7,8-tetramethoxyflavone has been researched along with 4'-hydroxy-5,6,7,8,3'-pentamethoxyflavone in 3 studies

Compound Research Comparison

Studies
(4',5-dihydroxy-3',6,7,8-tetramethoxyflavone)		Trials
(4',5-dihydroxy-3',6,7,8-tetramethoxyflavone)		Recent Studies (post-2010)
(4',5-dihydroxy-3',6,7,8-tetramethoxyflavone)		Studies
(4'-hydroxy-5,6,7,8,3'-pentamethoxyflavone)		Trials
(4'-hydroxy-5,6,7,8,3'-pentamethoxyflavone)		Recent Studies (post-2010) (4'-hydroxy-5,6,7,8,3'-pentamethoxyflavone)
6031508

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Autino, JC; Bennardi, DO; Castro, EA; Duchowicz, PR; Fernández, FM; Mercader, AG; Romanelli, GP1
Kosano, H; Miyata, Y; Natsugari, H; Okuyama, Y; Oshitari, T; Takahashi, H1
Kosano, H; Miyata, Y; Natsugari, H; Okuyama, Y; Oshitari, T; Shimada, A; Takahashi, H1

Other Studies

3 other study(ies) available for 4',5-dihydroxy-3',6,7,8-tetramethoxyflavone and 4'-hydroxy-5,6,7,8,3'-pentamethoxyflavone

ArticleYear
QSAR prediction of inhibition of aldose reductase for flavonoids.
    Bioorganic & medicinal chemistry, 2008, Aug-01, Volume: 16, Issue:15

    Topics: Aldehyde Reductase; Computer Simulation; Flavonoids; Molecular Structure; Predictive Value of Tests; Quantitative Structure-Activity Relationship

2008
B-Ring-modified and/or 5-demethylated nobiletin congeners: inhibitory activity against pro-MMP-9 production.
    Bioorganic & medicinal chemistry, 2011, Dec-01, Volume: 19, Issue:23

    Topics: Cell Line; Enzyme Precursors; Epithelial Cells; Flavones; Humans; Lens, Crystalline; Matrix Metalloproteinase 9; Matrix Metalloproteinase Inhibitors; Protease Inhibitors; Tetradecanoylphorbol Acetate; Tumor Necrosis Factor-alpha

2011
Polymethoxyflavones as agents that prevent formation of cataract: nobiletin congeners show potent growth inhibitory effects in human lens epithelial cells.
    Bioorganic & medicinal chemistry letters, 2013, Jan-01, Volume: 23, Issue:1

    Topics: Cataract; Cell Line; Cell Movement; Cell Proliferation; Citrus; Epithelial Cells; Flavones; Humans; Lens, Crystalline; Matrix Metalloproteinase 9; Structure-Activity Relationship

2013