Journal of Enzyme Inhibition and Medicinal Chemistry · 2014 · 65 citations · 20 references
PharmacyChemistryPharmacologyDrug DiscoveryOrganic ChemistryStructure-activity RelationshipsAntioxidant DefenseStructure-activity Relationship AnalysisAntioxidant Activity AssaysAntioxidant Capacity AssaysAntioxidant PropertiesMass Spectral Data AnalysisNatural AntioxidantsScavengingSynthetic AntioxidantsTriazole Chemistry
Various triheterocyclic compounds containing benzimidazole, thiophene, and 1,2,4-triazole rings (3-6) were synthesized and screened for their antioxidant activities. The structures of the synthesized compounds (2-6) were judged by (1)H NMR, (13)C NMR, elemental analysis, and LC-MS spectral data. Antioxidant activities of the synthesized compounds (2-6) were determined with CUPric Reducing Antioxidant Capacity (CUPRAC), ABTS (2,2-azinobis(3-ethylbenzothiazoline-6-sulfonic acid)/persulfate, and DPPH (1,1-diphenyl-2-picrylhydrazyl) assays. Most of the compounds showed a significant antioxidant activity and especially, compound 5c showed very good SC50 value for DPPH method and compound 5h exhibited very high scavenging activity to ABTS method.
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Use of a free radical method to evaluate antioxidant activity
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