Masaret Ghada S
Department of Chemistry, Faculty of Applied Science, Umm Al-Qura University, Makkah, Saudi Arabia.
J Mol Struct. 2022 Dec 5;1269:133581. doi: 10.1016/j.molstruc.2022.133581. Epub 2022 Jun 25.
Synthesis of a new series of spiropyrazole derivatives using microwaves irradiation with high yield in minutes was achieved through a cycloaddition reaction of nitrile imines and arylidenes of 5-bromo-indan-1-one. The structure of the new spiropyrazoles was assured based on their available spectral analyses and the comparison of the extracted data with the literature reports. Molecular docking simulations of all new synthesized spiropyrazole derivatives into leucyl-tRNA synthetase editing domain of (Pdb: 2WFC) indicated that about seven spiropyrazole derivatives can fit deeply in the active site the formation of stable complexes. In addition, the docking study was utilized to tested the ability of these spiropyrazoles to inhibit COVID-19 through the interaction with COVID-19 main protease (Pdb: 6LU7). The results were surprising which revealed high docking score ranging from -7.764 to -5.9464 kcal/mol. Moreover, the nitrogen atom of pyrazole, Br atom and the C=O group of indanone are essential parts in the binding mode of almost the active derivatives. The results of the docking study are a glimmer of hope to complete the study on these compounds and examine them in the laboratory to ensure their effectiveness as antimicrobials and antiviral, especially Covid-19. Moreover, pharmacokinetics and physicochemical properties were studied.
通过腈亚胺与5-溴茚满-1-酮的亚芳基的环加成反应,在几分钟内以高产率实现了一系列新的螺吡唑衍生物的微波辐射合成。基于现有的光谱分析以及将提取的数据与文献报道进行比较,确定了新螺吡唑的结构。对所有新合成的螺吡唑衍生物与(Pdb:2WFC)的亮氨酰-tRNA合成酶编辑结构域进行分子对接模拟表明,约七种螺吡唑衍生物可深入契合活性位点并形成稳定复合物。此外,利用对接研究来测试这些螺吡唑通过与COVID-19主要蛋白酶(Pdb:6LU7)相互作用抑制COVID-19的能力。结果令人惊讶,显示对接分数高达-7.764至-5.9464 kcal/mol。此外,吡唑的氮原子、溴原子和茚满酮的C=O基团几乎是所有活性衍生物结合模式中的关键部分。对接研究结果为完成对这些化合物的研究并在实验室中对其进行检测以确保其作为抗菌剂和抗病毒剂(尤其是针对新冠病毒)的有效性带来了一线希望。此外,还研究了它们的药代动力学和理化性质。