Investigating the antibacterial potential of thiophene derivatives against wound infections: a combined DFT, molecular docking, and ADMET study targeting Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli resistant genes.

In silico pharmacology Pub Date : 2024-11-20 eCollection Date: 2024-01-01 DOI:10.1007/s40203-024-00279-0
Mathias O Ajaba, Bassey E Agbo, Nse Umoh, Ekaette S Udoh, Alpha O Gulack, Andrew Ushie, Friday O Izachi, Bethel C Ateb
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Abstract

Wound infection poses a significant global health threat, as it is a leading cause of morbidity and mortality among surgical patients and individuals with burn injuries, resulting in substantial healthcare burdens and devastating outcomes worldwide. Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli have frequently been implicated as major pathogens causing wound infections. This has eventually and consistently given rise to antimicrobial resistance divulging a need to mitigate infectious outbreaks. Herein, we employed a computational density functional theory (DFT) method at ωB97XD/6-311++g(d, p) level of theory to evaluate the performance of the thiophene derivative 5-(4-bromo-5-(methylthio)thiophen-2-yl)-4-phenyl-4H-1,2,4-triazole-3-thiol 4, which is experimentally synthesized into five compounds (4a, 4b, 4c, 4d, and 4e). The chemical reactivity, kinetic stability, nature of interactions and functional characteristics of the thiophene derivatives were ascertained. The resistance gene PDB ID: 1K25, 2D45, 4UOT, and 7K2X were employed and docked with thiophene derivatives. Interestingly, molecular docking analysis demonstrated that ligands 4a, 4b, 4c, 4d, and 4e are more effective against proteins 1K25, 4U0T and 7K2X than amoxicillin and methicillin. Upon docking with the 2D45 protein, compounds 4c and 4e (- 5.9 kcal/mol) exhibited potential similar to that of methicillin (- 5.9 kcal/mol), while 4a and 4b showed slightly better affinities (- 6.1 kcal/mol and 6.0 kcal/mol). Using Lipinski's Rule of Five (Ghose filter, Veber rules, Muegge filter, and Egan's rule), 4d and 4e were determined to be the most promising candidates for drug development due to their compliance with all evaluated criteria, indicating favourable properties for oral bioavailability and drug likeness. This research suggested that thiophene derivatives can serve as promising antibacterial agents against wound-infected bacteria.

调查噻吩衍生物对伤口感染的抗菌潜力:针对金黄色葡萄球菌、绿脓杆菌和大肠杆菌耐药基因的 DFT、分子对接和 ADMET 联合研究。
伤口感染对全球健康构成重大威胁,因为它是外科手术患者和烧伤患者发病和死亡的主要原因,在全球范围内造成巨大的医疗负担和破坏性后果。金黄色葡萄球菌、铜绿假单胞菌和大肠杆菌经常被认为是导致伤口感染的主要病原体。这最终导致了抗菌药耐药性的不断产生,因此需要减少感染性疾病的爆发。在此,我们采用ωB97XD/6-311++g(d, p)理论水平下的密度泛函理论(DFT)计算方法,评估了噻吩衍生物 5-(4-溴-5-(甲硫基)噻吩-2-基)-4-苯基-4H-1,2,4-三唑-3-硫醇 4 的性能,实验合成了五个化合物(4a、4b、4c、4d 和 4e)。研究人员确定了噻吩衍生物的化学反应活性、动力学稳定性、相互作用性质和功能特征。采用抗性基因 PDB ID:1K25、2D45、4UOT 和 7K2X 与噻吩衍生物进行对接。有趣的是,分子对接分析表明,与阿莫西林和甲氧西林相比,配体 4a、4b、4c、4d 和 4e 对 1K25、4U0T 和 7K2X 蛋白更有效。在与 2D45 蛋白对接时,化合物 4c 和 4e 的亲和力(- 5.9 kcal/mol)与甲氧西林的亲和力(- 5.9 kcal/mol)相似,而 4a 和 4b 的亲和力稍好(- 6.1 kcal/mol 和 6.0 kcal/mol)。利用利宾斯基五法则(Ghose 过滤器、Veber 规则、Muegge 过滤器和 Egan 规则),4d 和 4e 被确定为最有希望进行药物开发的候选化合物,因为它们符合所有评估标准,表明它们具有良好的口服生物利用度和药物相似性。这项研究表明,噻吩衍生物可作为抗伤口感染细菌的抗菌剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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