新型吲哚-三唑共轭物的合成、分子对接和生物学评价。

Paras Berwal, Suman Rohilla, Nancy Mathur, Ketki Rani
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引用次数: 0

摘要

背景:吲哚-三唑共轭物已成为新药开发的有前途的候选化合物。吲哚-三唑共轭物具有独特的结构特征和广泛的生物活性,是研究新型药物的一个极具吸引力和前景的领域:本研究旨在合成吲哚-三唑共轭物,研究各种取代基对吲哚-三唑杂化物功能特性的影响。研究还旨在通过分子对接研究新杂交化合物与 DNA 回旋酶的结合模式:方法:合成了一组新的吲哚-三唑混合物,并利用各种理化和光谱分析对其进行了表征。所有杂交化合物都进行了体内药代动力学预测研究。采用试管稀释法和琼脂扩散法评估了杂交化合物的抗菌功效。此外,还使用 1,1-二苯基-2-苦基肼自由基清除试验测定了合成化合物的体外抗氧化活性。此外,还进行了硅学分子对接研究,以加深我们对合成化合物如何在分子水平上与 DNA 回旋酶相互作用的理解:结果:对合成的杂交化合物进行的药代动力学预测表明,这些化合物具有良好的药代动力学特征,而且没有一个化合物违反了利平斯基规则(Lipinski rule of five)。值得注意的是,以环己醇取代基为特征的化合物 6 显示出卓越的抗菌和抗氧化活性(EC50 值 = 14.23 μmol)。分子对接研究进一步支持了体外抗氧化和抗菌研究结果,揭示出所有化合物都能很好地进入 DNA 回旋酶的结合口袋,并与关键的氨基酸残基发生相互作用:总之,我们的研究强调了分子杂交在塑造新型吲哚三唑衍生物的物理化学、药代动力学和生物学特性方面的功效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, Molecular Docking, and Biological Evaluation of Novel Indole-triazole Conjugates.

Background: Indole-triazole conjugates have emerged as promising candidates for new drug development. Their distinctive structural characteristics, coupled with a wide array of biological activities, render them a captivating and promising field of research for the creation of novel pharmaceutical agents.

Objective: This study aimed to synthesize indole-triazole conjugates to investigate the influence of various substituents on the functional characteristics of indole-triazole hybrids. It also aimed to study the binding modes of new hybrids with the DNA Gyrase using molecular docking studies.

Methods: A new set of indole-triazole hybrids was synthesized and characterized using various physicochemical and spectral analyses. All hybrids underwent in-silico pharmacokinetic prediction studies. The antimicrobial efficacy of the hybrids was assessed using tube dilution and agar diffusion methods. Additionally, the in-vitro antioxidant activity of synthesized compounds was determined using the 1,1-diphenyl-2-picryl-hydrazyl free radical scavenging assay. Furthermore, in silico molecular docking studies were performed to enhance our comprehension of how the synthesized compounds interact at the molecular level with DNA gyrase.

Results: Pharmacokinetic predictions of synthesized hybrids indicated favourable pharmacokinetic profiles, and none of the compounds violated the Lipinski rule of five. Notably, compound 6, featuring a cyclohexanol substituent, demonstrated superior antimicrobial and antioxidant activity (EC50 value = 14.23 μmol). Molecular docking studies further supported the in vitro antioxidant and antimicrobial findings, revealing that all compounds adeptly fit into the binding pocket of DNA Gyrase and engaged in interactions with crucial amino acid residues.

Conclusion: In summary, our research underscores the efficacy of molecular hybridization in shaping the physicochemical, pharmacokinetic, and biological characteristics of novel indole-triazole derivatives.

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