首页> 外文期刊>Oncology Research >Structure-activity relationship of 9-methylstreptimidone, a compound that induces apoptosis selectively in adult T-cell leukemia cells
【24h】

Structure-activity relationship of 9-methylstreptimidone, a compound that induces apoptosis selectively in adult T-cell leukemia cells

机译:9-甲基链烷二酮的结构-活性关系,该化合物可选择性诱导成年T细胞白血病细胞凋亡

获取原文
获取原文并翻译 | 示例
       

摘要

We previously reported that 9-methylstreptimidone, a piperidine compound isolated from a culture filtrate of Streptomyces, induces apoptosis selectively in adult T-cell leukemia cells. It was screened for a compound that inhibits LPS-induced NF-κB and NO production in mouse macrophages. However, 9-methystreptimidone is poorly obtained from the producing microorganism and difficult to synthesize. Therefore, in the present research, we studied the structure-activity relationship to look for new selective inhibitors. We found that the structure of the unsaturated hydrophobic portion of 9-methylstreptimidone was essential for the inhibition of LPS-induced NO production. Among the 9-methylstreptimidone-related compounds tested, (±)-4,α-diepi-streptovitacin A inhibited NO production in macrophage-like cells as potently as 9-methylstreptimidone and without cellular toxicity. Moreover, this compound selectively induced apoptosis in adult T-cell leukemia MT-1 cells.
机译:我们先前曾报道过9-甲基链烷二酮是从链霉菌的培养滤液中分离出来的哌啶化合物,可选择性诱导成人T细胞白血病细胞凋亡。筛选了可抑制LPS诱导的小鼠巨噬细胞中NF-κB和NO生成的化合物。但是,从产生的微生物中很难获得9-甲基链霉素二酮,并且难以合成。因此,在本研究中,我们研究了结构-活性关系以寻找新的选择性抑制剂。我们发现,9-甲基链烷二酮的不饱和疏水部分的结构对于抑制LPS诱导的NO产生至关重要。在所测试的与9-甲基链烷二酮有关的化合物中,(±)-4,α-二烯-链霉维他命A与9-甲基链烷二酮一样有效地抑制巨噬细胞样细胞中的NO生成,并且没有细胞毒性。而且,该化合物选择性地诱导成年T细胞白血病MT-1细胞的凋亡。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号