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苯并咪唑衍生物抗菌活性研究 被引量:2

Antibacterial activity of benzimidazole derivatives
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摘要 以15种苯并咪唑衍生物为抑菌实验测试药品,以大肠杆菌、金色葡萄糖球菌等10种细菌作为受试菌种,通过平板法定性测定样品的抗菌活性。结果表明,除丁二苯并咪唑外,其他的化合物都表现出一定的抑菌活性。同时通过试管法定量测定了样品的最小抑菌浓度(MIC),实验结果表明,化合物对细菌都有较好的抑菌活性,其中2-(2-(1H-benzo[d]imidazol-2-yl)pyridin-3-yl)-1H-benzo[d]imidazole、2,3-吡啶二羧酸、1,2-di(1H-benzo[d]imidazol-2-yl)ethane-1,2-diol、2-phenyl-1H-benzo[d]imidazole具有广谱的抑菌活性,2,2’-联咪唑对枯草杆菌的MIC为0.8μg/m L,2,3-吡啶二羧酸对肺炎球菌的MIC为1.0μg/m L。 15 kinds of benzimidazole derivatives as antibacterial drug testing experiments, E. coli, and other 10 kinds of golden glucose cocci bacteria as bacteria tested by the statutory determination of the sample flat antibacterial activity. The results show that, in addition to succinic benzimidazole, other compounds have shown some antibacterial activity. Meanwhile through in vitro quantitative determination of the minimum inhibitory concentration of the sample(MIC), the experimental results show that the compounds of the bacteria have good antibacterial activity, including 2-(2-(1H-benzo [d] imidazol-2- yl) pyridin-3-yl)-1H- benzo [d] imidazole, 2,3- pyridinedicarboxylic acid, 1,2-di(1H-benzo [d] imidazol-2-yl) ethane-1,2- diol, 2-phenyl-1H-benzo [d] imidazole has a broad spectrum of antibacterial activity against Bacillus subtilis 2,2'-imidazole MIC was 0.8μg / m L, 2,3- dicarboxylic acid pyridine pneumococcal the MIC was 1.0μg / m L.
出处 《大众科技》 2015年第3期108-110,共3页 Popular Science & Technology
关键词 苯并咪唑衍生物 抗菌 最小抑菌浓度 Benzimidazole derivatives antibacterial minimum inhibitory concentration
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  • 1倪青玲,李发思,金伶伶,贺鹏喜,王修建.N,N′-二羧甲基-2-甲基苯并咪唑内鎓盐的合成及晶体结构[J].化学研究与应用,2007,19(11):1181-1184. 被引量:9
  • 2KATRITZKY A R, ASLAN D C, LEEMING P, et al. Asymmetric induction using chiral 1, 2, 4-triazole and benz- imidazole derivatives [J]. Tetrahedron : Asymmetry, 1997, 8(9): 1491-1500.
  • 3PATIL B G, HAVINALE B R, SHALLOM J M, et al. Syntheses and spectroscopic studies of potential antitumor copper( ]I ) complexes with 5 phenylazo-3-methoxy salicyli- dene thiosemicarbazone and N4 substituted thiosemicarba- zones [J]. Inorg Biochem, 1989, 36(2) : 107-113.
  • 4FERRARI M B, BISCEGLIE F, PELOSI G, et al. Synthe- sis, characterisation, X-ray structure and biological activity of three new 5-formyluracil thiosemicarbazone complexes [J]. Inorg Biochem, 2001, 83(2):169-179.
  • 5HERTZBERG R P, CARANFA M J, HECHT S M. On the mechanism of topoisomerase I inhibition by camptothecin: evidence for binding to an enzyme-DNA complex[J]. Bio- chemistry, 1989, 28(11): 4629-4638.
  • 6DHAR D, TOLMAN W B. Hydrogen atom abstraction from hydrocarbons by a copper ( 1]] )-hydroxide complex[J]. Jour-nal of the American Chemical Society, 2015, 137 ( 3 ).- 1322 1329.
  • 7SHEE N K, ADEKUNLE F A O, VERMA R, et el. A copper ( 1I ) complex with a Cu-S 8 bond. Attenuated total relectance, electron paramagnetic resonance, resonance Raman and atoms-in-molecule calculations[J]. Speetrochim- ice Acta Part A: Molecular and Biomolecular Spectroscopy, 2015, 151: 96-99.
  • 8SHELDRICK G M. SHELXL-97, Program for the Refine- ment of Crystal Structure [P]. Germany University of G5ttingen, 1997.
  • 9SONG W J, LIN Q Y, JIANG W J, et al. Synthesis, inter action with DNA and antiproliferative activities of two novel Cu ( II ) complexes with norcantharidin and benzimidazole derivatives[J]. Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy, 2015, 137 : 122-128.
  • 10ISMAIL Z K, EIDISSOUKY A, SHEHADA A Z. Spectro- scopic and magnetic studies on some copper( II ) complexes of antipyrine Schiff Base derivatives [J] . Polyhedron, 1997, 16(17)= 2909- 2916.

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