Design, Synthesis and Biological Evaluation of Ligustrazine-Flavonoid Derivatives as Potential Anti-Tumor Agents
In the clinic some anti-tumor drugs have shown damage to normal blood vessels, which could lead to vascular diseases. Therefore, it is necessary to evaluate the effects of anti-tumor drugs on normal blood vessels at the beginning of the drug design process. In this study, ligustrazine (TMP) and flavonoids were selected as raw materials. Sixteen novel TMP-flavonoid derivatives were designed and synthesized. Interestingly, compounds14and16were obtained by hydrolysis of a dihydroflavone to a chalcone under alkaline conditions. The cytotoxicity of the TMP-flavonoid derivatives was evaluated on five human tumor cell lines and one classical type of normal endothelial cell lines (HUVEC-12) by an MTT assay. Part of the derivatives showed better anti-tumor activities than the corresponding raw materials. Among them, compound14exhibited the closest activity to the positive control against the Bel-7402 cell line (IC50= 10.74 ± 1.12 μM; DDP IC50= 6.73 ± 0.37 μM) and had no toxicity on HUVEC-12 (IC50> 40 μM). Subsequently, fluorescence staining and flow cytometry analysis indicated that compound14could induce apoptosis of Bel-7402 cell lines. Moreover, the structure-activity relationships of these derivatives were briefly discussed.Keywords:TMP-flavonoid derivatives;anti-tumor;human tumor cell lines;HUVEC-12;fluorescence staining;flow cytometry
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