Kaddouri Yassine, Bouchal Btissam, Abrigach Farid, El Kodadi Mohamed, Bellaoui Mohammed, Elkamhawy Ahmed, Touzani Rachid, Abdellattif Magda H
Laboratory of Inorganic Chemistry, Department of Chemistry, University of Helsinki, P.O. Box 55, FI-00014 Helsinki, Finland.
Genetics Unit, Medical Sciences Research Laboratory, Faculty of Medicine and Pharmacy of Oujda, University Mohammed Premier, Oujda 11022, Morocco.
Pharmaceuticals (Basel). 2022 Jun 28;15(7):803. doi: 10.3390/ph15070803.
A new family of pyrazole-based compounds (-) was synthesized and characterized using different physicochemical analyses, such as FTIR, UV-Visible, H, C NMR, and ESI/LC-MS. The compounds were evaluated for their in vitro antifungal and antibacterial activities against several fungal and bacterial strains. The results indicate that some compounds showed excellent antibacterial activity against , , , and strains. In contrast, none of the compounds had antifungal activity. Molecular electrostatic potential (MEP) map analyses and inductive and mesomeric effect studies were performed to study the relationship between the chemical structure of our compounds and the biological activity. In addition, molecular docking and virtual screening studies were carried out to rationalize the antibacterial findings to characterize the modes of binding of the most active compounds to the active pockets of NDM1 proteins.
合成了一个基于吡唑的新化合物家族(-),并使用不同的物理化学分析方法进行了表征,如傅里叶变换红外光谱(FTIR)、紫外可见光谱、氢核磁共振(H NMR)、碳核磁共振(C NMR)以及电喷雾电离/液相色谱-质谱联用(ESI/LC-MS)。评估了这些化合物对几种真菌和细菌菌株的体外抗真菌和抗菌活性。结果表明,一些化合物对金黄色葡萄球菌、大肠杆菌、枯草芽孢杆菌和铜绿假单胞菌菌株表现出优异的抗菌活性。相比之下,这些化合物均无抗真菌活性。进行了分子静电势(MEP)图谱分析以及诱导效应和中介效应研究,以探究我们所合成化合物的化学结构与生物活性之间的关系。此外,还开展了分子对接和虚拟筛选研究,以合理化抗菌研究结果,从而表征最具活性的化合物与NDM1蛋白活性口袋的结合模式。