Alkaloids Lead to Potential Inhibition of the Acyl Carrier Protein Reductase to Attenuate Tuberculosis; an in-silico Analysis

Pernia Kamran, Ahsan Ibrahim
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引用次数: 0

Abstract

Tuberculosis (TB) is a contagious infection that mostly affects the lungs. Mycobacterium tuberculosis causes tuberculosis infection, leading to granulomatous lesions in affected lung tissue. It is one of the most prevalent and deadly infectious diseases among the under developed countries. This study aims to investigate the possible inhibition of the acyl carrier protein reductase for preventing tuberculosis by well-known alkaloids, thereby reducing Mycobacterium tuberculosis growth in the lungs and thereby reducing the incidence of latent and active TB. About five natural alkaloids were subjected to the molecular docking analysis, which produced favorable findings in terms of best pose and binding energies of these compounds towards the active residues of mycobacterial ACP reductase, with values ranging from -10 kcal/mol to -9.1 kcal/mol. The molecular dynamics simulation produced similar encouraging results. All of the prospective alkaloid compounds were subjected to an in-silico toxicity investigation, which determined that every compound was safe and non-toxic. Further studies may be necessary for effective formulation development employing these compounds as part of the process of drug discovery and development. The findings from this study may be helpful in the development of the novel nanoformulations using natural products for pharmacotherapy of tuberculosis infection.
生物碱对酰基载体蛋白还原酶的潜在抑制作用计算机分析
结核病(TB)是一种主要影响肺部的传染性感染。结核分枝杆菌引起结核感染,导致受感染的肺组织出现肉芽肿性病变。它是欠发达国家中最普遍和最致命的传染病之一。本研究旨在探讨知名生物碱可能对预防结核病的酰基载体蛋白还原酶的抑制作用,从而减少结核分枝杆菌在肺部的生长,从而降低潜伏性和活动性结核病的发病率。对5种天然生物碱进行了分子对接分析,得到了这些化合物与分枝杆菌ACP还原酶活性残基的最佳位态和结合能,其值在-10 ~ -9.1 kcal/mol之间。分子动力学模拟也产生了类似的令人鼓舞的结果。所有潜在的生物碱化合物都进行了硅毒性研究,确定每种化合物都是安全无毒的。作为药物发现和开发过程的一部分,利用这些化合物进行有效的配方开发可能需要进一步的研究。这项研究的发现可能有助于开发利用天然产物进行结核病感染药物治疗的新型纳米制剂。
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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