Utilization of 2-cyano-N-(2,5-dioxopyrrolidin-1-yl) acetamide for the synthesis of thiazole, pyrazole and pyridene derivatives with a biological evaluation

IF 2.2 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Mohamed Ahmed Mahmoud Abdel Reheim, Ibrahim Saad Abdel Hafiz, Reem Mustafa Darweesh, Sayeda Abdelrazek Abdelhamid, Mohamed Ahmed Elian Sophy
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引用次数: 0

Abstract

A range of fused heterocyclic compounds are generated utilizing the crucial intermediary 2-cyano-N-(2,5-dioxopyrrolidin-1-yl) acetamide 4. Spectral analysis was executed to support the structures of the newly synthesized compounds, which is expected to have a potential biological activity. The antimicrobial activity of the recently synthesized compounds and their derivatives has been tested against B. subtilis, S. aureus, E. coli, P. aeruginosa, S. typhimurium, C. albicans, and A. niger, as reference antibiotics, ampicillin and mycostatin, were used against test bacteria and fungi, respectively. In general, the novel produced compounds demonstrated a good antibacterial action against the previously indicated pathogens.

Abstract Image

利用 2-氰基-N-(2,5-二氧代吡咯烷-1-基)乙酰胺合成噻唑、吡唑和吡啶衍生物并进行生物学评价
利用关键中间体 2-氰基-N-(2,5-二氧代吡咯烷-1-基)乙酰胺 4 生成了一系列融合杂环化合物。光谱分析证实了新合成化合物的结构,预计这些化合物具有潜在的生物活性。最近合成的化合物及其衍生物对枯草杆菌、金黄色葡萄球菌、大肠杆菌、铜绿假单胞菌、鼠伤寒杆菌、白僵菌和黑曲霉的抗菌活性进行了测试。总的来说,所生产的新型化合物对上述病原体具有良好的抗菌作用。
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来源期刊
CiteScore
4.40
自引率
8.30%
发文量
230
审稿时长
5.6 months
期刊介绍: JICS is an international journal covering general fields of chemistry. JICS welcomes high quality original papers in English dealing with experimental, theoretical and applied research related to all branches of chemistry. These include the fields of analytical, inorganic, organic and physical chemistry as well as the chemical biology area. Review articles discussing specific areas of chemistry of current chemical or biological importance are also published. JICS ensures visibility of your research results to a worldwide audience in science. You are kindly invited to submit your manuscript to the Editor-in-Chief or Regional Editor. All contributions in the form of original papers or short communications will be peer reviewed and published free of charge after acceptance.
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