首页> 外文期刊>American Journal of Analytical Chemistry >Synthesis, Characterization and Bioactivity of 1,1-bis(2-Carbamoylguanidino)furan-2-ylmethane
【24h】

Synthesis, Characterization and Bioactivity of 1,1-bis(2-Carbamoylguanidino)furan-2-ylmethane

机译:1,1-双(2-氨基甲酰基胍亚胺)呋喃-2-基甲烷的合成,表征和生物活性

获取原文
           

摘要

This study reports the synthesis of 1,1-bis(2-Carbamoylguanidino)furan-2-ylmethane, characterisation and bioactivities on selected microorganism. The first step involves the coupling of furfural with urea to obtain 1-((2-carbamoylguanidino)(furan-2-ylmethyl)urea, which was subsequently refluxed with more urea in ethanol for 1 hour to afford the product. Both intermediate and product were characterized by GC-MS, IR, ~(1)H-NMR, ~(13)C-NMR. The synthesized compound1,1-bis(2-carbamoylguanidino)furan-2-ylmethane was bioactive on Escherichia coli, Salmomellatyphi and Bacillus subtilis to different extent and is inactive on Staphylococcus aureus. The presences of bioactive moieties and pharmacological activities have proved the potency of furfural derivatives in the development of novel drug in future.
机译:本研究报告了1,1-双(2-氨基甲酰胍亚胺烷烃)呋喃-2-基甲烷,表征和生物活性的合成。第一步涉及糠醛与尿素的偶联,得到1-((2-氨基甲酰胍亚胺氨基)(Furan-2-基甲基)尿素,随后用更多的乙醇中的尿素回流1小时,得到产物。中间和产品通过GC-MS,IR,〜(1)H-NMR,〜(13)C-NMR。合成化合物1,1-双(2-氨基甲酰基)呋喃-2-基甲烷在大肠杆菌,Salmomellyphi和Salmomellyphi和枯草芽孢杆菌在不同程度上并且在金黄色葡萄球菌上无活性。生物活性部分和药理活动的潜在未来在新型药物发展中证明了糠醛衍生物的效力。

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