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Curcumin and Natural Derivatives Inhibit Ebola Viral Proteins: An In silico Approach

机译:姜黄素和天然衍生物抑制埃博拉病毒蛋白:计算机方法

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Background: Ebola viral disease is a severe and mostly fatal disease in humans caused by Ebola virus. This virus belongs to family Filoviridae and is a single-stranded negative-sense virus. There is no single treatment for this disease which puts forth the need to identify new therapy to control and treat this fatal condition. Curcumin, one of the bioactives of turmeric, has proven antiviral property. Objective: The current study evaluates the inhibitory activity of curcumin, bisdemethoxycurcumin, demethoxycurcumin, and tetrahydrocurcumin against Zaire Ebola viral proteins (VPs). Materials and Methods: Molecular simulation of the Ebola VPs followed by docking studies with ligands comprising curcumin and related compounds was performed. Results: The highest binding activity for VP40 is ?6.3 kcal/mol, VP35 is ?8.3 kcal/mol, VP30 is ?8.0 kcal/mol, VP24 is ?7.7 kcal/mol, glycoprotein is ?7.1 kcal/mol, and nucleoprotein is 6.8 kcal/mol. Conclusion: Bisdemethoxycurcumin shows better binding affinity than curcumin for most VPs. Metabolite tetrahydrocurcumin also shows binding affinity comparable to curcumin. These results indicate that curcumin, curcuminoids, and metabolite tetrahydrocurcumin can be potential lead compounds for developing a new therapy for Ebola viral disease. SUMMARY Curcumin, bisdemethoxycurcumin, and demethoxycurcumin are active constituents of turmeric. Tetrahydrocurcumin is the major metabolite of curcumin formed in the body after consumption and absorption of curcuminoids Curcuminoids have proven antiviral activity Bisdemethoxycurcumin showed maximum inhibition of Ebola viral proteins (VPs) among the curcuminoids in the docking procedure with a docking score as high as ?8.3 kcal/mol Tetrahydrocurcumin showed inhibitory activity against Ebola VPs close to that of curcumin’s inhibitory action. Abbreviations Used: EBOV: Ebola virus, GP: Glycoprotein, NP: Nucleoprotein, NPT: Isothermal-isobaric Ensemble, amount of substance (N), pressure (P) and temperature (T) conserved, NVE: Canonical ensemble, amount of substance (N), volume (V) and temperature (T) conserved, VP: Viral protein.
机译:背景:埃博拉病毒病是由埃博拉病毒引起的一种严重的人类致命疾病。该病毒属于丝虫科,是单链负义病毒。没有针对这种疾病的单一治疗方法,因此需要确定新的治疗方法来控制和治疗这种致命疾病。姜黄素是姜黄的生物活性物质之一,已被证明具有抗病毒特性。目的:本研究评估姜黄素,双去甲氧基姜黄素,去甲氧基姜黄素和四氢姜黄素对扎伊尔埃博拉病毒蛋白(VPs)的抑制活性。材料和方法:对埃博拉病毒VPs进行分子模拟,然后与包含姜黄素和相关化合物的配体对接研究。结果:对VP40的最高结合活性为?6.3 kcal / mol,VP35为?8.3 kcal / mol,VP30为?8.0 kcal / mol,VP24为?7.7 kcal / mol,糖蛋白为?7.1 kcal / mol,而核蛋白为6.8大卡/摩尔。结论:对于大多数VP,双去甲氧基姜黄素显示出比姜黄素更好的结合亲和力。代谢物四氢姜黄素也显示出与姜黄素相当的结合亲和力。这些结果表明,姜黄素,姜黄素和代谢物四氢姜黄素可能是开发针对埃博拉病毒病的新疗法的潜在先导化合物。发明内容姜黄素,双去甲氧基姜黄素和去甲氧基姜黄素是姜黄的活性成分。四氢姜黄素是姜黄素的主要代谢产物,在食用和吸收姜黄素后被体内形成。姜黄素已被证明具有抗病毒活性。双去甲氧基姜黄素在对接过程中对姜黄素中的埃博拉病毒蛋白(VPs)的抑制作用最大,对接得分高达8.3 kcal。 / mol四氢姜黄素对埃博拉病毒VPs的抑制活性接近姜黄素的抑制作用。使用的缩写:EBOV:埃博拉病毒,GP:糖蛋白,NP:核蛋白,NPT:等温-等压集合体,守恒的物质(N),压力(P)和温度(T),NVE:规范的合奏,物质的数量( N),体积(V)和温度(T)保守,VP:病毒蛋白。

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