水溶性咪唑功能化柱[5]芳烃的制备及其抗菌、抗氧化、催化还原4-硝基苯酚的活性研究

IF 4.5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Keziban Atacan , Alican Bahadır Semerci , Nuray Güy , Nubar Mammadova , Mustafa Ozmen , Ahmed Nuri Kursunlu
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引用次数: 0

摘要

柱[n]芳烃等大环超分子材料通过主客体相互作用在增强抗菌活性方面发挥着重要作用。本文制备了水溶性柱状[5]芳烃咪唑-1和柱状[5]芳烃咪唑-2,并通过多种表征方法对其结构和化学成分进行了分析。随后,检测了所制备的咪唑功能化柱b[5]芳烃对大肠杆菌、粪肠球菌、金黄色葡萄球菌和鼠伤寒沙门菌的抑菌活性。并用2,2-二苯基-1-吡啶酰肼考察了所制备的咪唑功能化柱[5]芳烃的抗氧化活性。此外,还研究了柱状[5]芳烃咪唑-1和柱状[5]芳烃咪唑-2还原4-硝基苯酚的催化活性,表明柱状[5]芳烃咪唑-1催化剂在18 min时对4-硝基苯酚的催化还原率为93.0%。柱状[5]芳烃咪唑-1与柱状[5]芳烃咪唑-2的反应活性比较表明,柱状[5]芳烃咪唑-1的抑菌活性和催化活性均有所提高。本研究总结了采用合适的催化剂,催化还原的目的是将最有害、最有毒的有机化合物4-硝基苯酚转化为无毒的4-氨基苯酚,并在工业上推广应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Preparation of water-soluble imidazole-functionalized pillar[5]arenes: The activities of antibacterial and antioxidant, catalytic reduction of 4-nitrophenol

Preparation of water-soluble imidazole-functionalized pillar[5]arenes: The activities of antibacterial and antioxidant, catalytic reduction of 4-nitrophenol
Macrocyclic supramolecular materials such as pillar[n]arenes play a prominent role in enhancing antibacterial activity through host-guest interactions. Herein, the water-soluble pillar[5]arene imidazole-1 and pillar[5]arene imidazole-2 were prepared, and their structure and chemical compositions were analyzed through multiple characterization methods. Afterward, the prepared imidazole-functionalized pillar[5]arenes were examined for antibacterial activity against Escherichia coli, Enterococcus faecalis, Staphylococcus aureus, and Salmonella typhimurium bacteria. Also, the antioxidant activities of the prepared imidazole-functionalized pillar[5]arenes were investigated using 2,2-Diphenyl-1-picrylhydrazyl. In addition, the catalytic activities of pillar[5]arene imidazole-1 and pillar[5]arene imidazole-2 by reduction of 4-nitrophenol were studied, indicating the catalytic reduction of 4-nitrophenol was 93.0 % for the pillar[5]arene imidazole-1 catalyst at 18 min. Comparison of the reactivity of pillar[5]arene imidazole-1 with that of pillar[5]arene imidazole-2 shows an increase in antibacterial and catalytic activity. This study summarized that using suitable catalysts, catalytic reduction aims to convert the most harmful and toxic organic compound 4-nitrophenol into non-toxic 4-aminophenol and popularize it in industry.
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来源期刊
Bioorganic Chemistry
Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
9.70
自引率
3.90%
发文量
679
审稿时长
31 days
期刊介绍: Bioorganic Chemistry publishes research that addresses biological questions at the molecular level, using organic chemistry and principles of physical organic chemistry. The scope of the journal covers a range of topics at the organic chemistry-biology interface, including: enzyme catalysis, biotransformation and enzyme inhibition; nucleic acids chemistry; medicinal chemistry; natural product chemistry, natural product synthesis and natural product biosynthesis; antimicrobial agents; lipid and peptide chemistry; biophysical chemistry; biological probes; bio-orthogonal chemistry and biomimetic chemistry. For manuscripts dealing with synthetic bioactive compounds, the Journal requires that the molecular target of the compounds described must be known, and must be demonstrated experimentally in the manuscript. For studies involving natural products, if the molecular target is unknown, some data beyond simple cell-based toxicity studies to provide insight into the mechanism of action is required. Studies supported by molecular docking are welcome, but must be supported by experimental data. The Journal does not consider manuscripts that are purely theoretical or computational in nature. The Journal publishes regular articles, short communications and reviews. Reviews are normally invited by Editors or Editorial Board members. Authors of unsolicited reviews should first contact an Editor or Editorial Board member to determine whether the proposed article is within the scope of the Journal.
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