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Synthesis, characterization and antibacterial activity of novel heterocycle, coumacine, and two of its derivatives

机译:新型杂环,香豆素及其两种衍生物的合成,表征和抗菌活性

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Heterocyclic nucleus plays a fundamental role in the medicinal chemistry and serves as a key template for the development of various therapeutic agents including broad spectrum antibacterial drugs. In an effort to develop new antibacterial agents, a bicyclic twelve-membered heterocyclic nucleus derived from coumarin was prepared by an uncomplicated method. The rate of ring closure for this nucleus, which was given the name coumacine, in addition to two of its derivatives was monitored spectroscopically and this rate followed zero order kinetics. The chemical structures of the synthesized products were established by detecting their physicochemical properties and analyzing their IR, 1H NMR and 13C NMR spectra. The in vitro antibacterial activity of coumacines was evaluated via agar dilution method against different standard aerobic and anaerobic bacterial strains using ciprofloxacin and metronidazole as positive controls, respectively; the results indicated that coumacine I has an excellent broad spectrum antibacterial activity against the tested bacterial strains with percentage of growth inhibition approximating to those of positive controls.
机译:杂环核在药物化学中起着基本作用,并且是开发包括广谱抗菌药物在内的各种治疗药物的关键模板。为了开发新的抗菌剂,通过简单的方法制备了衍生自香豆素的双环十二元杂环核。用光谱法监测该核的闭环速率,除了其两个衍生物外,还被命名为香豆素,并且该速率遵循零级动力学。通过检测其理化性质并分析其IR,1H NMR和13C NMR光谱,可以确定合成产物的化学结构。通过琼脂稀释法分别以环丙沙星和甲硝唑为阳性对照,通过琼脂稀释法评估香豆素的体外抗菌活性对不同的标准好氧和厌氧细菌菌株的影响。结果表明,香豆素I对被测细菌菌株具有优异的广谱抗菌活性,其生长抑制百分比接近阳性对照。

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