a College of Chemistry and Chemical Engineering , Hunan University , Changsha , China.
Nat Prod Res. 2019 Sep;33(17):2440-2445. doi: 10.1080/14786419.2018.1448812. Epub 2018 Mar 27.
Two series of fifteen novel thioxoflavonoids and were synthesized from corresponding flavonoids and by reacting with Lawesson's reagent, respectively. Their antiproliferative activities were evaluated on a panel of three human cancer cell lines (Hela, HCC1954 and SK-OV-3) using cell counting kit-8 (CCK-8) assay. The results showed that most of the target compounds exhibited moderate to good antiproliferative activities against the three human cancer cell lines. In particular, thioxoflavonoids and showed the strongest antiproliferative activity on all three human cancer cell lines with IC values ranging from 3.34 to 4.67 μM, showed the best antiproliferative activity on Hela cells (IC 2.30 μM), showed the best antiproliferative activity on HCC1954 cells (IC 2.13 μM) and SK-OV-3 cells (IC 2.33 μM). The antiproliferative activities may be involved in their antioxidant activity, which can be speculated by their ability to scavenge free radicals and by their capacity of affecting key redox enzymes.
两个系列共 15 个新型的噻二芳基呋喃酮类化合物 和 分别通过与劳森试剂反应,由相应的黄酮类化合物 和 合成。采用细胞计数试剂盒(CCK-8)检测法,评估了这些化合物对三种人癌细胞系(Hela、HCC1954 和 SK-OV-3)的增殖抑制活性。结果表明,大多数目标化合物对三种人癌细胞系均表现出中等至良好的增殖抑制活性。特别是噻二芳基呋喃酮类化合物 和 对所有三种人癌细胞系的增殖抑制活性最强,IC 值范围为 3.34-4.67 μM;化合物 对 Hela 细胞的增殖抑制活性最好(IC 2.30 μM);化合物 对 HCC1954 细胞(IC 2.13 μM)和 SK-OV-3 细胞(IC 2.33 μM)的增殖抑制活性最好。增殖抑制活性可能与其抗氧化活性有关,可以通过其清除自由基的能力和影响关键氧化还原酶的能力来推测。