首页> 美国卫生研究院文献>Springer Open Choice >Synthesis antibacterial and antiproliferative potential of some new 1-pyridinecarbonyl-4-substituted thiosemicarbazide derivatives
【2h】

Synthesis antibacterial and antiproliferative potential of some new 1-pyridinecarbonyl-4-substituted thiosemicarbazide derivatives

机译:一些新的1-吡啶羰基-4-取代的硫代氨基脲衍生物的合成抗菌和抗增殖潜力

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

In this study, the antibacterial, cytotoxic and antiproliferative activities of novel thiosemicarbazide derivatives were assessed. Our results demonstrated that some of the novel compounds possess good antibacterial properties against Staphylococcus epidermidis, Streptococcus mutans and Streptococcussanguinis and are only slightly cytotoxic; thus, they exhibit an excellent therapeutic index, which is higher than that of ethacridine lactate. Moreover, our data showed that compounds >2 and >4 have an antiproliferative activity against human breast adenocarcinoma and human hepatocellular carcinoma cell lines. We expect that the novel thiosemicarbazide derivatives can be used as agents for treatment of dental caries and also for chemotherapy support.Electronic supplementary materialThe online version of this article (doi:10.1007/s00044-016-1599-6) contains supplementary material, which is available to authorized users.
机译:在这项研究中,评估了新型硫代氨基脲衍生物的抗菌,细胞毒性和抗增殖活性。我们的结果表明,某些新型化合物对表皮葡萄球菌,变形链球菌和血链球菌具有良好的抗菌性能,并且仅具有轻微的细胞毒性。因此,它们显示出优异的治疗指数,高于乳酸乙肝啶。而且,我们的数据表明化合物> 2 和> 4 对人乳腺癌和人肝癌细胞系具有抗增殖活性。我们希望新的硫代氨基脲衍生物可以用作治疗龋齿和化疗支持的药物。电子补充材料本文的在线版本(doi:10.1007 / s00044-016-1599-6)包含补充材料,即可供授权用户使用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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