valproic acid and zopolrestat

valproic acid has been researched along with zopolrestat in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's3 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bezakova, Z; Carbone, V; Demopoulos, V; Djoubissie, PO; El-Kabbani, O; Karasu, C; Majekova, M; Rackova, L; Snirc, V; Stefek, M1
Heine, A; Klebe, G; Majekova, M; Rechlin, C; Soltesova Prnova, M; Stefek, M1
Ballekova, J; Majekova, M; Prnova, M; Stefek, M1
Akber Ansari, S; Arote, R; Chhajed, S; Pathan, SK; Patil, R; Sangshetti, J; Shinde, DB1

Reviews

1 review(s) available for valproic acid and zopolrestat

ArticleYear
Synthesis and biological activity of structurally diverse phthalazine derivatives: A systematic review.
    Bioorganic & medicinal chemistry, 2019, 09-15, Volume: 27, Issue:18

    Topics: Humans; Phthalazines

2019

Other Studies

3 other study(ies) available for valproic acid and zopolrestat

ArticleYear
Carboxymethylated pyridoindole antioxidants as aldose reductase inhibitors: Synthesis, activity, partitioning, and molecular modeling.
    Bioorganic & medicinal chemistry, 2008, May-01, Volume: 16, Issue:9

    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
Identification of novel aldose reductase inhibitors based on carboxymethylated mercaptotriazinoindole scaffold.
    Journal of medicinal chemistry, 2015, Mar-26, Volume: 58, Issue:6

    Topics: Acetic Acid; Aldehyde Reductase; Animals; Crystallography, X-Ray; Enzyme Inhibitors; Humans; Indoleacetic Acids; Lens, Crystalline; Male; Models, Molecular; Rats; Rats, Wistar; Sorbitol; Structure-Activity Relationship; Sulfhydryl Compounds

2015
Structure optimization of tetrahydropyridoindole-based aldose reductase inhibitors improved their efficacy and selectivity.
    Bioorganic & medicinal chemistry, 2017, 12-15, Volume: 25, Issue:24

    Topics: Aldehyde Reductase; Animals; Dose-Response Relationship, Drug; Enzyme Inhibitors; Indoles; Male; Molecular Structure; Quantum Theory; Rats; Rats, Wistar; Structure-Activity Relationship

2017