首页> 外文期刊>International Journal of Pure & Applied Chemistry >Synthesis and characterization of(2E)-1-[(6-nitro-1,3-benzoxazol-2-yl) sulfanyl]propan-2-one iV-[(lZ)-(4-chlorophenyl) methylidene] thiosemicarbazone Benzoxazole Derivatives and their biological Activities
【24h】

Synthesis and characterization of(2E)-1-[(6-nitro-1,3-benzoxazol-2-yl) sulfanyl]propan-2-one iV-[(lZ)-(4-chlorophenyl) methylidene] thiosemicarbazone Benzoxazole Derivatives and their biological Activities

机译:(2E)-1 - [(6-硝基-1,3-苯并恶唑-2-基)磺酰基]丙丹-2-一IV - [(LZ) - (4-氯苯基)甲基]硫代吡嗪苯并恶唑衍生物的合成与表征 及其生物活动

获取原文
获取原文并翻译 | 示例
           

摘要

In this study a new series of(2E)-1-[(6-nitro-1,3-benzoxazol-2-yl)sulfanyl]propan-2-one N-[(1Z)-(4-chloroyphenyl)methylidene]thiosemicarbazone derivatives have been synthesized by standard physicochemical methods.The structures of newly synthesized benzoxazole derivatives(5_(a-f)) were characterized by elemental analysis,FT-IR,~1H NMR,~(13)C NMR and mass spectral studies.The synthesized compounds(5_(a-f)) has been screened for their antimicrobial activity using the disc diffusion and minimum inhibitory concentration(MIC) method against the selected bacterias(Staphylococcus aureus,Staphylococcus epidemidis,Bacillus subtilis,P.aeruginosa,Vibrio cholerae and E.coli) and fungal strain(Aspergillus aureus and Aspergillus fumigates).Among all synthesized benzoxazole derivatives 5b,5c,5d and 5f were found to be more potent antibacterial active against all tested strains.The In vitro antimicrobial activity at MIC level showed that the compound 5a also exhibit potent antimicrobial activity as similar to compound 5c.The antioxidant properties were evaluated by 2,2-diphenyl-1-picrylhydrazyl(DPPH) scavenging method.Compounds 5a and 5b showed predominant antioxidant activities among the synthesized analogues.
机译:在本研究中,新系列(2E)-1 - [(6-硝基-1,3-苯并恶唑-2-基)磺酰基]丙烷-2-一N - [(1Z) - (4-氯苯基)亚甲基]已经通过标准物理化学方法合成了硫代吡嗪衍生物。通过元素分析,FT-IR,〜1H NMR,〜(13)C NMR和质谱研究,表征了新合成的苯并恶唑衍生物(5_(AF))的结构。合成已经使用椎间盘扩散和最小抑制浓度(MIC)方法筛选化合物(5_(AF))对所选择的菌血(金黄色葡萄球菌,葡萄球菌癫痫,枯草芽孢杆菌,P.Aeruginosa,Vibrio Cholerae和E.Coli)来筛选它们的抗微生物活性)和真菌菌株(Aspergillus aureus和aspergillus熏蒸)。大声均合成苯并恶唑衍生物5b,5c,5d和5f,对所有测试菌株进行更有效的抗菌活性。MIC水平的体外抗微生物活性显示化合物5a还表现出有效的抗菌活性作为SI单独的化合物5C。通过2,2-二苯基-1-富铬酰基(DPPH)清除方法,评价抗氧化性能.. POUND 5A和5B在合成类似物中显示出主要的抗氧化活性。

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