Zhang Shun, An Baijiao, Li Jiayan, Hu Jinhui, Huang Ling, Li Xingshu, Chan Albert S C
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Org Biomol Chem. 2017 Sep 13;15(35):7404-7410. doi: 10.1039/c7ob01655g.
Sixteen new selenium-containing indole chalcone and diarylketone derivatives were synthesized and evaluated as tubulin polymerization inhibitors. Among them, compound 25b exhibited the most potent antiproliferative activities against six human cancer cell lines with IC values of 0.004-0.022 μM. A microtubule dynamics assay and an immunofluorescence assay confirmed that 25b could effectively inhibit tubulin polymerization (IC = 2.1 ± 0.27 μM). Further cellular mechanism studies revealed that 25b induced G2/M phase arrest, which was further evidenced by the decrease in the mitochondrial membrane potential (MMP).
合成了16种新型含硒吲哚查尔酮和二芳基酮衍生物,并将其作为微管蛋白聚合抑制剂进行评估。其中,化合物25b对六种人类癌细胞系表现出最有效的抗增殖活性,IC值为0.004 - 0.022μM。微管动力学测定和免疫荧光测定证实,25b可有效抑制微管蛋白聚合(IC = 2.1±0.27μM)。进一步的细胞机制研究表明,25b诱导G2/M期阻滞,线粒体膜电位(MMP)降低进一步证明了这一点。