Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1367516 | Bioorganic & Medicinal Chemistry Letters | 2006 | 4 Pages |
The antioxidant properties of substituted diarylamines in the benzo[b]thiophene series were evaluated by their reducing power and free radical scavenging activity. The results were compared with those of standards: acid ascorbic for the first method and BHA and BHT for the second. For both methods it was possible to establish some structure–activity relationships (SARs) based on the position of the arylamination on the benzo[b]thiophene moiety, the presence of different substituents on the phenyl ring (F, 1 or 2 OMe) and on the thiophene ring (H, CO2Et, CO2H).
Graphical abstractChemical assays for the determination of the reducing power and free radical scavenging activity of the diarylamines are presented.Figure optionsDownload full-size imageDownload as PowerPoint slide