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Antioxidant and Antitumor Activities of Newly Synthesized Hesperetin Derivatives
Authors:Guanlin Zhong  Jiayi Shen  Zhengwang Chen  Zunxian Lin  Lipeng Long  Jiaying Wu  Chenhuan Long  Siyu Huang  Ping Lian  Guotian Luo
Institution:Key Laboratory of Organo-Pharmaceutical Chemistry of Jiangxi Province, Gannan Normal University, Ganzhou 341000, China; (G.Z.); (Z.C.); (Z.L.); (L.L.); (J.W.); (C.L.); (S.H.); (P.L.)
Abstract:Hesperetin is a class of natural products with a wide range of sources and remarkable biological activities. In this study, we described the synthesis of a series of novel hesperetin derivatives and evaluated the in vitro antioxidant and antitumor activity of these compounds. Eleven novel compounds were synthesized in moderate yields. The compounds synthesized in this work exhibited antioxidant activities against DPPH and ABTS free radicals in a dose-dependent manner. Among them, compound 3f had the best antioxidant activity, with IC50 of 1.2 μM and 24 μM for DPPH and ABTS, respectively. The antitumor activity of the compounds against human cancer cell lines, such as breast MCF-7, liver HepG2, and cervical Hela, was determined by a standard 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) assay. Three compounds had moderate IC50 values. Interestingly, compound 3f had better biological activity than hesperetin, which matches the prediction by Maestro from Schrödinger. Therefore, the new hesperidin derivative is a promising drug for the treatment of cancer due to its effective antitumor activity. The results also suggested that the antitumor activities of hesperetin derivatives may be related to their antioxidant activities.
Keywords:hesperetin derivatives  aminobenzene methylation  antioxidant activity  antitumor activity  structure–  activity relationships  molecular docking
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