Tamilarasi W, Balamurugan B J
Department of Mathematics, School of Advanced Sciences, Vellore Institute of Technology, Chennai, Tamil Nadu, India.
Front Chem. 2024 Dec 19;12:1486933. doi: 10.3389/fchem.2024.1486933. eCollection 2024.
Ebola and Marburg viruses, biosafety level 4 pathogens, cause severe hemorrhaging and organ failure with high mortality. Although some FDA-approved vaccines or therapeutics like Ervebo for Zaire Ebola virus exist, still there is a lack of effective therapeutics that cover all filoviruses, including both Ebola and Marburg viruses. Therefore, some anti-filovirus drugs such as Pinocembrin, Favipiravir, Remdesivir and others are used to manage infections. In theoretical chemistry, a chemical molecule is converted into an isomorphic molecular graph, ( ) by considering atom set as vertices and bond set as edges. A topological index is a molecular descriptor derived from the molecular graph of a chemical compound that characterizes its topology. The relationship between a compound's chemical structure and its properties is investigated through the quantitative structure-property relationship (QSPR). This article introduces new reverse sum Revan degree based indices to explore the physicochemical and pharmacokinetic properties of anti-filovirus drugs via multilinear regression. The findings reveal a strong correlation between these proposed indices and the properties of anti-filovirus drugs when compared to reverse and Revan degree-based indices. Thus, reverse sum Revan indices offer valuable insights for analyzing the drugs properties used to treat Ebola and Marburg virus infections. Moreover, the multilinear regression (MLR) results through reverse sum Revan indices are compared with Artificial Neural Network (ANN) modelling technique and it provides the better prediction of the physicochemical and pharmacokinetic properties of anti-filovirus drugs.
埃博拉病毒和马尔堡病毒属于生物安全4级病原体,可导致严重出血和器官衰竭,死亡率很高。尽管存在一些美国食品药品监督管理局(FDA)批准的疫苗或治疗药物,如用于治疗扎伊尔埃博拉病毒的Ervebo,但仍然缺乏涵盖所有丝状病毒(包括埃博拉病毒和马尔堡病毒)的有效治疗方法。因此,一些抗丝状病毒药物,如松属素、法匹拉韦、瑞德西韦等被用于控制感染。在理论化学中,通过将原子集视为顶点、键集视为边,将化学分子转化为同构分子图。拓扑指数是从化合物的分子图派生出来的分子描述符,用于表征其拓扑结构。通过定量结构-性质关系(QSPR)研究化合物的化学结构与其性质之间的关系。本文引入了基于新的逆和Revan度的指数,通过多元线性回归探索抗丝状病毒药物的物理化学和药代动力学性质。研究结果表明,与基于逆度和Revan度的指数相比,这些提出的指数与抗丝状病毒药物的性质之间存在很强的相关性。因此,逆和Revan指数为分析用于治疗埃博拉和马尔堡病毒感染的药物性质提供了有价值的见解。此外,将基于逆和Revan指数的多元线性回归(MLR)结果与人工神经网络(ANN)建模技术进行了比较,结果表明它能更好地预测抗丝状病毒药物的物理化学和药代动力学性质。