Analyze the Sombor Index of Molecular Graphs Representing Antibiotic Drugs Using the ℳ Polynomial.

J Senbagamalar, M S Ramani, Venkata Shivakumar Remella
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Abstract

Introduction: Today's world is grappling with numerous infectious diseases and pandemics caused by bacteria, viruses, fungi, or parasites, which are affecting people at an alarming rate. Molecular topology, a field that significantly influences drug design and discovery, involves the algebraic description of chemical compounds, enabling their distinctive and straightforward characterization.

Materials and methods: Among various applications, the topological indices can be generated from ℳ-polynomial. ℳ-polynomial is a generating function that has been proposed to unify the computation of diverse topological indices. It contains degree-based topological data of molecular graphs and facilitates the derivation of multiple degree-based topological indices in an efficient manner. The ℳ-polynomial can be used to derive different degree-based topological indices by using different transformations. Computational efficiency offers a common method for calculating several topological indices. QSAR/QSPR Models are employed to examine molecular properties and biological activity in drug design.

Results: The Sombor index, a molecular descriptor, was studied in the context of several antibacterial medications, including Amoxicillin, Ampicillin, Tetracycline, Doxycycline, Cefalexin, and Ciprofloxacin. These drugs are commonly used to treat conditions such as bladder infections, rickettsial infections, pneumonia, bronchitis, and other respiratory tract infections.

Discussion: In this study, the edge partition technique is employed to derive the ℳ-polynomial for selected antibacterial drug molecules. The graphical representation of the respective molecular structures is calculated and discussed based on the derived ℳ-polynomial.

Conclusion: To construct the ℳ -polynomial and derive the Sombor index for antibiotic drugs, then correlate them with the physicochemical properties of these drugs to analyze the regression models for the best fit.

用多项式法分析抗生素药物分子图的Sombor指数。
导言:当今世界正在努力应对由细菌、病毒、真菌或寄生虫引起的众多传染病和大流行病,这些疾病正以惊人的速度影响着人们。分子拓扑学是一个影响药物设计和发现的重要领域,它涉及化合物的代数描述,使其具有独特和直接的表征。材料与方法:在各种应用中,拓扑指标可以由ℳ;-多项式生成。-多项式是一种生成函数,用于统一各种拓扑指标的计算。它包含了分子图的基于度的拓扑数据,便于高效地推导多个基于度的拓扑指标。-多项式可以通过使用不同的变换来导出不同的基于度数的拓扑索引。计算效率为计算几种拓扑指标提供了一种通用的方法。QSAR/QSPR模型用于检测药物设计中的分子特性和生物活性。结果:研究了分子描述符Sombor指数在阿莫西林、氨苄西林、四环素、多西环素、头孢氨苄星、环丙沙星等几种抗菌药物中的应用。这些药物通常用于治疗膀胱感染、立克次体感染、肺炎、支气管炎和其他呼吸道感染等疾病。讨论:本研究采用边缘分割技术对所选抗菌药物分子进行ℳ;-多项式推导。基于导出的ℳ;-多项式,计算和讨论了各自分子结构的图形表示。结论:构建抗生素药物的ℳ;-多项式,导出抗生素药物的Sombor指数,并将其与药物的理化性质进行关联,分析回归模型的最佳拟合。
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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