Hu Laixing, Jiang Jian-dong, Qu Jinrong, Li Yan, Jin Jie, Li Zhuo-rong, Boykin David W
Department of Chemistry, Georgia State University, Atlanta, GA 30303-3083, USA.
Bioorg Med Chem Lett. 2007 Jul 1;17(13):3613-7. doi: 10.1016/j.bmcl.2007.04.048. Epub 2007 Apr 25.
We report the synthesis, antiproliferative activity, and SAR of novel heterocyclic ketones derived from carbazole sulfonamides. Most of the heterocyclic ketones showed strong cytotoxicities. (N-1-Methylindole-5-yl)-(3,4,5-trimethoxyphenyl)-methanone 8b gave the most potent cytotoxicity (9.2-26 nM) against seven human tumor cell lines. The mechanism of action of the heterocyclic ketones appears to involve targeting of tubulin, similar to that of CA-4 and different from the carbazole sulfonamides.
我们报道了源自咔唑磺酰胺的新型杂环酮的合成、抗增殖活性及构效关系。大多数杂环酮表现出较强的细胞毒性。(N-1-甲基吲哚-5-基)-(3,4,5-三甲氧基苯基)-甲酮8b对七种人类肿瘤细胞系具有最强的细胞毒性(9.2 - 26 nM)。杂环酮的作用机制似乎涉及靶向微管蛋白,这与CA-4类似,与咔唑磺酰胺不同。