Kyoto Pharmaceutical University.
Cancer Chemotherapy Center, Japanese Foundation for Cancer Research.
Chem Pharm Bull (Tokyo). 2022;70(11):823-826. doi: 10.1248/cpb.c22-00574.
Here, we synthesized three acetogenin analogs containing pyrimidine moieties linked by amine bonds, which represent the skeleton structure of pyrimidifen, a mitochondrial complex I-inhibiting insecticide. Replacing the pyrimidine moiety linked by the amine bond remarkably enhanced growth-inhibitory activity of the analogs against several human cancer cell lines. Moreover, these analogs selectively and potently inhibited the growth of these human cancer cell lines regardless of the pyrimidine substituents. Furthermore, COMPARE analyses suggested that these analogs inhibited cancer growth by inhibiting mitochondrial complex I. Our study provides insights into the design of acetogenin analogs as novel antitumor agents.
在这里,我们合成了三种含有嘧啶部分的乙酰辅酶 A 类似物,它们通过胺键连接,代表了嘧啶芬(一种抑制线粒体复合物 I 的杀虫剂)的骨架结构。取代通过胺键连接的嘧啶部分显著增强了类似物对几种人癌细胞系的生长抑制活性。此外,这些类似物选择性地、有效地抑制了这些人癌细胞系的生长,而与嘧啶取代基无关。此外,比较分析表明,这些类似物通过抑制线粒体复合物 I 抑制肿瘤生长。我们的研究为设计新型抗肿瘤乙酰辅酶 A 类似物提供了思路。