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The thiosemicarbazone derivatives have a wide range of biological activities, such as antioxidant activity. In this study, the antiradical activities of six camphene-based thiosemicarbazones (<b>TSC-1~6</b>) were investigated by 2,2-diphenyl-1-picrylhydrazyl (DPPH) and peroxyl radical scavenging capacity (PSC) assays, respectively, and the results reveal that <b>TSC1~6</b> exhibited good abilities for scavenging free radicals in a dose-dependent way. Compound <b>TSC-2</b> exhibited the best effect of scavenging DPPH radical, with the lowest EC₅₀ (0.208 &#177; 0.004 mol/mol DPPH) as well as the highest bimolecular rate constant K_b (4218 M^&#8722;1 s^&#8722;1), which is 1.18-fold higher than that of Trolox. Meanwhile, <b>TSC-2</b> also obtained the lowest EC₅₀ (1.27 &#181;mol of Trolox equiv/&#181;mol) of scavenging peroxyl radical. Furthermore, the density functional theory (DFT) calculation was carried out to further explain the experimental results by calculating several molecular descriptors associated with radical scavenging activity. These theoretical data suggested that the electron-donating effect of the diethylamino group in <b>TSC-2</b> leads to the enhancement of the scavenging activities and the studied compounds may prefer to undergo the hydrogen atom transfer process.