国际药物开发与研究杂志

  • 国际标准期刊号: 0975-9344
  • 期刊 h 指数: 44
  • 期刊引用分数: 59.93
  • 期刊影响因子: 48.80
索引于
  • Genamics 期刊搜索
  • 中国知网(CNKI)
  • 引用因子
  • 西马戈
  • 研究期刊索引目录 (DRJI)
  • OCLC-WorldCat
  • 普布隆斯
  • 米亚尔
  • 大学教育资助委员会
  • 欧洲酒吧
  • 谷歌学术
  • 夏尔巴罗密欧
  • 秘密搜索引擎实验室
  • 研究之门
分享此页面

抽象的

Synthesis, Characterization, and Antibacterial Activity two New Schiff Bases devired from (E)-2-(((2-aminoethyl) imino) methyl) phenol (E)-2-(4-aminobut-1-enyl)-5-methylbenzamine

Sheheryar* and Mohib Ullah Shah

In this study two new Schiff base ligands were synthesized, characterized and antibacterial activities were investigated against Escherichia coli, Pseudomonas aeruginosa, Bacillus cereus, Salmonella typhimurium, and Staphylococcus aureus. (E)-2-(4-aminobut-1-enyl) phenol derived from Ethylene diamine and Salicyldehye. (E)-2-(4-aminobut-1-enyl)-5-methylaniline derived from 4-dimethyl amino benzaldehyde and Ethylene di-amine. The Schiff bases were characterized by elemental analysis and FT-IR. The Schiff base ligands were screened in vitro for their antibacterial inhibiting potential by using Disc diffusion method. The results indicated that the Schiff base I have showed biological activity against E coli. The main purpose of the study was to compare the inhibitory effect of these Schiff bases with commercial antibiotics Ciprofloxacin and Erythromycin to introduce new varieties of antibacterial agents.

Keywords

Schiff base; Antibacterial; FT-IR; Chemical synthesis