ACTA FAC MED NAISS 2020;37(4): 381-386

Original article

 

UDC: 541: 542.943

DOI: 10.5937/afmnai37-27103

 

 

In Vitro Antioxidant Properties of 2-Imino-benzimidazole
and 1,3-Thiazolo[3,2-a]benzimidazolone Derivatives

 

Katarina Tomović1, Jelena Mrmošanin2, Denitsa Yancheva3,
Anelia Ts Mavrova4, Andrija Šmelcerović5

1University of Niš, Faculty of Medicine, Department of Pharmacy, Niš, Serbia
2University of Niš, Faculty of Sciences and Mathematics, Department of Chemistry, Niš, Serbia
3Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences, Sofia, Bulgaria
4University of Chemical Technology and Metallurgy, Sofia, Bulgaria
5University of Niš, Faculty of Medicine, Department of Chemistry, Niš, Serbia

 

 

 SUMMARY

                                   

               Antioxidant properties of 2-[2-imino-5-nitro-3-(2-oxo-2-phenylethyl)-2,3-dihydro-1H-benzimidazol-1-yl]-1-phenylethanone (compound 1) and 2-(4-fluorobenzylidene)-6-(phenylcarbonyl)[1,3]thiazolo[3,2-a]benzimidazol-3(2H)-one (compound 2) were evaluated in vitro. Compounds 1 and 2 did not show significant radical scavenging activity. It has been suggested that antioxidant strategies should not be based on direct scavengers but rather on the potentiation of endogenous antioxidant defenses, or on the reduction of the sources of reactive species. Although a direct scavenging mechanism is missing, the assayed compounds (1 and 2) as evidenced inhibitors of xanthine oxidase and dipeptidyl peptidase-4 might act antioxidatively by employing other mechanisms.

 

Key words: 2-imino-benzimidazoles, 1,3-thiazolo[3,2-a]benzimidazolones, antioxidant activity, antioxidant mechanisms