新型5-甲基吲哚-2,3-二酮衍生物螺β-内酰胺的合成、表征及SAR研究

Q2 Chemistry Current Chemistry Letters Pub Date : 2022-01-01 DOI:10.5267/j.ccl.2022.5.001
P. Mondal, S. Mondal
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引用次数: 2

摘要

以新的希夫碱Isatin为原料,采用Staudinger合成法合成了一系列新的5-甲基吲哚-2,3-二酮衍生物的螺旋环-吲哚基β-内酰胺化合物。利用FT-IR, 1H-NMR, 13C-NMR,质谱和元素分析来描述所生产的化学物质。用标准阿苯达唑评价所制化合物的驱虫药效。通过杯盘法计算抑菌区,并与标准品氨苄西林比较,对枯草芽孢杆菌(ATCC-1086)、金黄色假单胞菌(ATCC-1232)、大肠杆菌(ATCC-3273)、变形杆菌(ATCC-224)和金黄色葡萄球菌(ATCC-449) 5种不同病原菌的抑菌活性进行了测试。驱虫电位结果显示,与常规阿苯达唑(PT: 1.324±0.12,DT: 1.421±0.21)相比,合成化合物ICP-3B (PT: 1.883±0.24,DT: 1.943±0.02)和ICM-3B (PT: 1.758±0.27,DT: 1.675±0.32)在麻痹和死亡时间方面具有显著活性。在抗菌研究中,与标准氨苄青霉素(23.04 mm区)相比,化合物ICP-3B在100µg/mL时对枯草芽孢杆菌有20.53mm的明显抑制区。在100 μ g/mL浓度下,化合物ICM-3B对枯草芽孢杆菌、铜绿假单胞菌、大肠杆菌、奇异变形杆菌和金黄色葡萄球菌的抑制范围分别为21.27 mm、24.64 mm、20.62mm和23.65 mm。根据所收集的光谱和元素数据,证实了化合物的合成符合预期。所获得的驱虫药抗蚁效果也肯定了所合成化合物的潜力。进一步的化合物可以被合成,也可以用分子模型的概念来测试这些化合物的其他药理活性。
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Synthesis, characterization and SAR studies of Novel Series of Spiro β-Lactam of 5-methyl-indole-2,3-dione derivatives as a potential antibacterial and anthelmintic agent
A novel series of spiro cyclo-indolyl β-lactam compounds of the 5-methyl-indole-2,3-dione derivatives has been synthesized from the new Schiff bases Isatin, using the Staudinger synthesis. FT-IR, 1H-NMR, 13C-NMR, mass spectroscopy, and elemental analyses were used to describe the produced chemicals. The anthelmintic potency of the produced compounds was evaluated using standard albendazole. The antibacterial activity also tested for the synthesized compounds by calculating the zone of inhibition using cup plate method and by comparison with the standard Ampicillin against the five different pathogens (Bacillus subtilis (ATCC-1086), Pseudomonas auroginosa (ATCC-1232), Escherichia coli, (ATCC-3273), Proteus mirabilis (ATCC-224), and Staphylococcus aureus (ATCC-449)). The result of anthelmintic potential, when compared to conventional albendazole (PT: 1.324±0.12, DT: 1.421±0.21), synthesized compounds ICP-3B (PT: 1.883±0.24, DT: 1.943±0.02) and ICM-3B (PT: 1.758±0.27, DT: 1.675±0.32) were shown significant activity in terms of paralysis and death time. In the antibacterial study, the compound ICP-3B has shown 20.53mm clear zone of inhibition at 100 µg/mL against the bacteria Bacillus subtilis in comparison to the standard ampicillin (23.04 mm zone). The compound ICM-3B, clearly shows the inhibition zone of 21.27 mm against Bacillus subtilis, 24.64 mm against pseudomonas aeruginosa, 20.62mm against E. coli, 20.41 mm against Proteus mirabilis and 23.65 mm against the bacteria staphylococcus aureus at the level of 100µg/mL. It was confirmed that the compounds were synthesized as expected in the reaction scheme based on the collected spectrum and elemental data. The obtained anthelmintic ant antibacterial results also affirm the potentiality of the synthesized compounds. The further compounds can be synthesised as well as other pharmacological activities can be tested for these compounds with the concept of molecular modelling.
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来源期刊
Current Chemistry Letters
Current Chemistry Letters Chemistry-Chemistry (all)
CiteScore
4.90
自引率
0.00%
发文量
27
审稿时长
20 weeks
期刊介绍: The "Current Chemistry Letters" is a peer-reviewed international journal which aims to publish all the current and outstanding research articles, reviews and letters in chemistry including analytical chemistry, green chemistry, inorganic chemistry, organic chemistry, physical chemistry, etc. This journal is dedicated to serve all academic and industrial researchers and scientists who are expert in all major advances in chemistry research. The journal aims to provide the most complete and reliable source of information on current developments in these fields. The emphasis will be on publishing quality articles rapidly and openly available to researchers worldwide. Please note readers are free to read, download, copy, distribute, print, search, or link to the full texts of articles published on this journal. Current Chemistry Letters is an open access journal, which provides instant access to the full text of research papers without any need for a subscription to the journal where the papers are published. Therefore, anyone has the opportunity to copy, use, redistribute, transmit/display the work publicly and to distribute derivative works, in any sort of digital form for any responsible purpose, subject to appropriate attribution of authorship. Authors who publish their articles may also maintain the copyright of their articles.
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