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首页> 外文期刊>Research journal of pharmacy and technology >Synthesis and Biological Evaluation of some 2,5-disubstituted 1,3,4-oxadiazole based Cinnoline derivatives
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Synthesis and Biological Evaluation of some 2,5-disubstituted 1,3,4-oxadiazole based Cinnoline derivatives

机译:基于2,5-二取代的1,3,4-二唑基唑类衍生物的合成与生物学评价

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Multiple drug resistance has developed due to the indiscriminate use of commercial antimicrobial drugs commonly used in the treatment of infectious diseases. In addition to this problem, antibiotics are sometimes associated with adverse effects on the host including hypersensitivity, immune suppression and allergic reaction. In order to overcome the current lacuna in the treatment of infectious diseases potential antimicrobial agents are in crucial need, therefore a Series of 3-(5-substituted-l,3,4-oxadiazol-2-yl)-6-fluoro cinnolin-4-ol were synthesized from 4-hydroxy-6-fluoro cinnoline-3-carbohydrazide. The structures of the newly synthesized compounds were confirmed by IR, NMR. All the compounds were screened for their antibacterial and antifungal activity against various pathogenic microbes. Synthesised compounds displayed very good antibacterial and antifungal activity remaining compounds showed moderate to good activity.
机译:由于常用于治疗传染病的商业抗微生物药物的滥用使用,多种耐药性已经开发出多种耐药性。 除了这个问题之外,抗生素有时与宿主的不利影响有关,包括过敏,免疫抑制和过敏反应。 为了克服目前的空格在治疗传染病的情况下,潜在的抗微生物剂是至关重要的,因此一系列3-(5-取代-1,3,4-恶二唑-2-基)-6-氟cinolin- 4-OL由4-羟基-6-氟葡萄奈碱-3-碳水化物合成。 通过IR,NMR确认新合成化合物的结构。 将所有化合物筛选对各种致病微生物的抗菌和抗真菌活性。 合成化合物显示出非常好的抗菌和抗真菌活性剩余的化合物显示中等至良好的活性。

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