valproic acid has been researched along with 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 2 (66.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bezakova, Z; Carbone, V; Demopoulos, V; Djoubissie, PO; El-Kabbani, O; Karasu, C; Majekova, M; Rackova, L; Snirc, V; Stefek, M | 1 |
Demopoulos, VJ; Koukoulitsa, C; Nicolaou, I; Pegklidou, K | 1 |
Alexiou, P; Demopoulos, VJ | 1 |
3 other study(ies) available for valproic acid and 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid
Article | Year |
---|---|
Carboxymethylated pyridoindole antioxidants as aldose reductase inhibitors: Synthesis, activity, partitioning, and molecular modeling.
Topics: Aldehyde Reductase; Animals; Antioxidants; Carbolines; Computer Simulation; Drug Evaluation, Preclinical; Enzyme Inhibitors; Hydrogen-Ion Concentration; Kinetics; Male; Methylation; Models, Molecular; Molecular Structure; Rats; Rats, Wistar; Static Electricity; Stereoisomerism; Structure-Activity Relationship; Time Factors | 2008 |
Design and synthesis of novel series of pyrrole based chemotypes and their evaluation as selective aldose reductase inhibitors. A case of bioisosterism between a carboxylic acid moiety and that of a tetrazole.
Topics: Aldehyde Reductase; Animals; Carboxylic Acids; Drug Design; Enzyme Inhibitors; Female; Male; Molecular Structure; Pyrroles; Rats; Rats, Inbred F344; Stereoisomerism; Structure-Activity Relationship; Tetrazoles | 2010 |
A diverse series of substituted benzenesulfonamides as aldose reductase inhibitors with antioxidant activity: design, synthesis, and in vitro activity.
Topics: Aldehyde Reductase; Animals; Antioxidants; Benzene Derivatives; Drug Design; Female; Free Radical Scavengers; In Vitro Techniques; Lipid Peroxidation; Male; Rats; Rats, Inbred F344; Stereoisomerism; Structure-Activity Relationship; Sulfonamides | 2010 |