首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Synthesis and evaluation of naphthalene-based thiosemicarbazone derivatives as new anticancer agents against LNCaP prostate cancer cells
【24h】

Synthesis and evaluation of naphthalene-based thiosemicarbazone derivatives as new anticancer agents against LNCaP prostate cancer cells

机译:萘基硫代半碳胺衍生物作为新型抗LNCaP前列腺癌细胞的抗癌药的合成与评价

获取原文
获取原文并翻译 | 示例
       

摘要

Fourteen new naphthalene-based thiosemicarbazone derivatives were designed as anticancer agents against LNCaP human prostate cancer cells and synthesized. MTT assay indicated that compounds 6, 8 and 11 exhibited inhibitory effect on LNCaP cells. Among these compounds, 4-(naphthalen-1-yl)-1-[1-(4-hydroxyphenyl)ethylidene)thiosemicarbazide (6), which caused more than 50% death on LNCaP cells, was chosen for flow cytometric analysis of apoptosis. Flow cytometric analysis pointed out that compound 6 also showed apoptotic effect on LNCaP cells. Compound 6 can be considered as a promising anticancer agent against LNCaP cells owing to its potent cytotoxic activity and apoptotic effect.
机译:设计了十四种新的基于萘的硫代半碳酰胺衍生物作为抗LNCaP人前列腺癌细胞的抗癌剂,并进行了合成。 MTT测定表明化合物6、8和11对LNCaP细胞表现出抑制作用。在这些化合物中,选择了导致LNCaP细胞死亡超过50%的4-(萘-1-基)-1- [1-(4-羟基苯基)亚乙基)硫代氨基脲(6)用于细胞凋亡的流式细胞分析。 。流式细胞仪分析指出,化合物6也显示出对LNCaP细胞的凋亡作用。化合物6由于其强大的细胞毒性活性和凋亡作用,可以被认为是针对LNCaP细胞的有希望的抗癌剂。

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