Page last updated: 2024-09-04

fidarestat and 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid

fidarestat has been researched along with 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid in 1 studies

Compound Research Comparison

Studies
(fidarestat)
Trials
(fidarestat)
Recent Studies (post-2010)
(fidarestat)
Studies
(6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid)
Trials
(6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid)
Recent Studies (post-2010) (6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid)
973331,54116580

Protein Interaction Comparison

ProteinTaxonomyfidarestat (IC50)6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (IC50)
Prostaglandin G/H synthase 1Homo sapiens (human)0.13
Prostaglandin G/H synthase 2Homo sapiens (human)0.15

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Demopoulos, VJ; Nicolaou, I1

Other Studies

1 other study(ies) available for fidarestat and 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid

ArticleYear
Substituted pyrrol-1-ylacetic acids that combine aldose reductase enzyme inhibitory activity and ability to prevent the nonenzymatic irreversible modification of proteins from monosaccharides.
    Journal of medicinal chemistry, 2003, Jan-30, Volume: 46, Issue:3

    Topics: Acetates; Aldehyde Reductase; Animals; Diabetes Mellitus; Enzyme Inhibitors; Female; Fructose; Male; Monosaccharides; Oxidation-Reduction; Proteins; Pyrroles; Rats; Rats, Inbred F344; Serum Albumin; Structure-Activity Relationship

2003