首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >l-(3-Aminomethyl-4-hydroxyphenyl)-3-pyridinyl-2-propen-l-ones: A novel group of tumour-selective cytotoxins
【24h】

l-(3-Aminomethyl-4-hydroxyphenyl)-3-pyridinyl-2-propen-l-ones: A novel group of tumour-selective cytotoxins

机译:L-(3-氨基甲基-4-羟基苯基)-3-吡啶基-2-丙烯 - L-液:一种新型肿瘤选择性细胞毒素组

获取原文
获取原文并翻译 | 示例
           

摘要

Two series of 1-(3-aminomethyl-4-hydroxyphenyl)-3-pyridinyl-2-propen-1-ones, designed as novel cytotoxins, were synthesized. The compounds had low CC_(50) values in the micromolar range against HL-60 promyelocytic leukemic cells and HSC-2, HSC-3 and HSC-4 oral squamous cell carcinomas. The CC_(50) values of these compounds were higher towards non-malignant HGF (gingival fibroblasts), HPC (pulp cells), and HPLF (periodontal ligament fibroblasts) cells, which reveals the tumour-selectivity of these enones. A representative compound 4c caused cleavage of PARP1 in HSC-2 cells but not in HGF cells, which may be a contributing factor to the tumour-selectivity.
机译:合成了设计为新型细胞毒素的两种1-(3-氨基甲基-4-羟基苯基)-3-吡啶基-2-丙烯-1- 1-酮。 该化合物在微摩尔范围内具有低CC_(50)值,用于针对HL-60幼高细胞白血病细胞和HSC-2,HSC-3和HSC-4口腔鳞状细胞癌。 这些化合物的CC_(50)值朝向非恶性HGF(牙龈成纤维细胞),HPC(纸浆细胞)和HPLF(牙周性韧带成纤维细胞)细胞较高,其揭示了这些肿瘤的肿瘤选择性。 代表性化合物4c在HSC-2细胞中引起PARP1的切割,但不引起HGF细胞,其可能是肿瘤选择性的贡献因素。

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