Juyal Vijay Kumar, Thakuri Shweta Chand, Panwar Mohit, Prakash Om, Perveen Kahkashan, Bukhari Najat A, Nand Viveka
Department of Chemistry, G.B. Pant University of Agriculture and Technology, Pantnagar, India.
Regional Ayurveda Research Institute, Ministry of Ayush, Gwalior, India.
Front Chem. 2024 Jul 19;12:1414646. doi: 10.3389/fchem.2024.1414646. eCollection 2024.
A new bidentate Schiff base ligand (CHClN), condensation product of ethylene diamine and 4-chloro N-phenyl formamide, and its metal complexes [M(CHClN)(OAc)] (where M = Mn(II) and Zn(II)) were synthesized and characterized using various analytical and spectral techniques, including high-resolution mass spectrometry (HRMS), elemental analysis, ultraviolet-visible (UV-vis), Fourier-transform infrared (FTIR) spectroscopy, AAS, molar conductance, H NMR, and powder XRD. All the compounds were non-electrolytes and nanocrystalline. The synthesized compounds were assessed for antioxidant potential by DPPH radical scavenging and FRAP assay, with BHT serving as the positive control. Inhibitory concentration at 50% inhibition (IC) values were calculated and used for comparative analysis. Furthermore, the prepared compounds were screened for antibacterial activity against two Gram-negative bacteria ( and ) and two Gram-positive bacteria ( and ) using disk-diffusion methods, with amikacin employed as the standard reference. The comparison of inhibition zones revealed that the complexes showed better antibacterial activity than the ligand. To gain insights into the molecular interactions underlying the antibacterial activity, the ligand and complexes were analyzed for their binding affinity with tyrosyl-tRNA synthetase (PDB ID: 1JIL) and cell membrane protein OmpF complex (PDB ID: 4KR4). These analyses revealed robust interactions, validating the observed antibacterial effects against the tested bacterial strains.
一种新型双齿席夫碱配体(CHClN),即乙二胺与4-氯-N-苯基甲酰胺的缩合产物,及其金属配合物[M(CHClN)(OAc)](其中M = Mn(II)和Zn(II))已通过多种分析和光谱技术合成并表征,这些技术包括高分辨率质谱(HRMS)、元素分析、紫外可见(UV-vis)光谱、傅里叶变换红外(FTIR)光谱、原子吸收光谱(AAS)、摩尔电导率、核磁共振氢谱(H NMR)和粉末X射线衍射(XRD)。所有化合物均为非电解质且为纳米晶体。通过DPPH自由基清除和FRAP测定法评估合成化合物的抗氧化潜力,以丁基羟基甲苯(BHT)作为阳性对照。计算出50%抑制率(IC)时的抑制浓度值并用于比较分析。此外,使用纸片扩散法对制备的化合物针对两种革兰氏阴性菌( 和 )和两种革兰氏阳性菌( 和 )进行抗菌活性筛选,以阿米卡星作为标准参考。抑菌圈的比较表明,配合物显示出比配体更好的抗菌活性。为了深入了解抗菌活性背后的分子相互作用,分析了配体和配合物与酪氨酰-tRNA合成酶(PDB ID:1JIL)和细胞膜蛋白OmpF复合物(PDB ID:4KR4)的结合亲和力。这些分析揭示了强烈的相互作用,证实了对测试细菌菌株观察到的抗菌效果。