From Isoniazid to 2-Pyrazolines: Synthesis, In silico Behaviour and Antimicrobial Activity

Q4 Chemistry Asian Journal of Chemistry Pub Date : 2024-07-25 DOI:10.14233/ajchem.2024.31666
Geetha Birudala, Gurinderdeep Singh, S. A. R. Junaid Nayeem, S. Padmavathi, Srinivasa Rao Pingali, Vaishali, R. Dighe
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Abstract

This study explores the synthesis, in silico behaviour and antimicrobial activity of isoniazid derived 2-pyrazolines as potential drugs for tuberculosis and bacterial infections. The investigation encompasses the synthesis, computational studies for molecular behaviour and antimicrobial efficacy assessment. Incorporating established drugs like isoniazid is explored to enhance their pharmacological properties. The synthesized compounds were characterized by analytical techniques such as IR, NMR, mass spectral analysis and elemental analysis. Synthesized pyrazolines 4a-j were evaluated for in vitro antitubercular and antibacterial activities against various biological strains. In silico analysis provides valuable insights into ADMET descriptors, confirming good pharmacokinetic properties. This suggests these compounds as templates for developing new anti-mycobacterial agents, guiding the design of novel compounds with improved therapeutic potential.
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从异烟肼到 2-吡唑啉类:合成、硅行为和抗菌活性
本研究探讨了异烟肼衍生的 2-吡唑啉类化合物的合成、硅学行为和抗菌活性,这些化合物是治疗结核病和细菌感染的潜在药物。研究包括合成、分子行为计算研究和抗菌效果评估。研究还探讨了与异烟肼等已有药物的结合,以增强其药理特性。通过红外光谱、核磁共振、质谱分析和元素分析等分析技术对合成的化合物进行了表征。对合成的吡唑啉类化合物 4a-j 进行了体外抗结核和抗菌活性评估。硅学分析为 ADMET 描述因子提供了有价值的见解,证实了这些化合物具有良好的药代动力学特性。这表明这些化合物可以作为开发新的抗霉菌药物的模板,指导设计具有更好治疗潜力的新型化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Asian Journal of Chemistry
Asian Journal of Chemistry 化学-化学综合
CiteScore
0.80
自引率
0.00%
发文量
229
审稿时长
4 months
期刊介绍: Information not localized
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