2- 苯基咪唑衍生物非共价相互作用分析的实验和理论研究:抗炎活性展望

IF 2.6 3区 化学 Q2 CHEMISTRY, ORGANIC Polycyclic Aromatic Compounds Pub Date : 2025-02-07 Epub Date: 2024-09-18 DOI:10.1080/10406638.2024.2403543
Manima Mishra , Amit Jaiswal , Murli Dhar Mitra , Ranjeet Kumar
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引用次数: 0

摘要

合成了2-苯基咪唑衍生物,对其非共价相互作用和抗炎活性进行了定量研究。Hirshfeld表面分析、晶体结构和非共价相互作用计算都被用于非共价相互作用的定量研究。分子间相互作用的计算是用crystalexplorer 17完成的。进一步,通过autodock静脉分子对接研究和卡拉胶大鼠体内实验,评价合成分子的抗炎活性。分子对接和体内研究表明,与标准药物尼美舒利相比,所有分子都显示出显著的抗炎活性。
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Experimental and Theoretical Studies for Noncovalent Interactions Analysis of 2-Phenyl Imidazole Derivative: Perspective for Anti-Inflammatory Activity
Synthesis of 2-Phenyl imidazole derivative has been carried out for the studies of quantitative non-covalent interactions and anti-inflammatory activity. Hirshfeld surface analysis, crystal structure, and non-covalent interaction computation have all been used to do quantitative investigations of non-covalent interactions. The intermolecular interactions calculations have been done with crystalexplorer 17. Further, anti-inflammatory activities of synthesized molecules were evaluated by molecular docking studies through autodock vina and in-vivo studies through carrageenan rat model. The molecular docking and in-vivo studies revealed that all molecules have shown significant anti-inflammatory activity, compared to standard drugs nimesulide.
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来源期刊
Polycyclic Aromatic Compounds
Polycyclic Aromatic Compounds 化学-有机化学
CiteScore
3.70
自引率
20.80%
发文量
412
审稿时长
3 months
期刊介绍: The purpose of Polycyclic Aromatic Compounds is to provide an international and interdisciplinary forum for all aspects of research related to polycyclic aromatic compounds (PAC). Topics range from fundamental research in chemistry (including synthetic and theoretical chemistry) and physics (including astrophysics), as well as thermodynamics, spectroscopy, analytical methods, and biology to applied studies in environmental science, biochemistry, toxicology, and industry. Polycyclic Aromatic Compounds has an outstanding Editorial Board and offers a rapid and efficient peer review process, as well as a flexible open access policy.
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