Molecular Descriptor Analysis of Certain Isomeric Natural Polymers. (24th August 2021)

• Record Type: Journal Article
• Authors: Ahmad, Maqsood; Saeed, Muhammad; Javaid, Muhammad; Bonyah, Ebenezer
• Other Names: Singh Ajaya Kumar Academic Editor.
• Is Part Of: Journal of chemistry. Volume 2021(2021)
• Publication Date: 2021-08-24
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1155/2021/9283246
• Languages: English
• ISSNs: 2090-9063

Abstract

Abstract : Polymers, drugs, and almost all chemical or biochemical compounds are frequently modeled as diverse ω -cyclic, acyclic, bipartite, and polygonal shapes and regular graphs. Molecular descriptors (topological indices) are the numerical quantities and computed from the molecular graph Γ (2D lattice). These descriptors are highly significant in quantitative structure-property or activity relationship (QSPR and QSAR) modeling that provides the theoretical and the optimal basis to expensive experimental drug design. In this paper, we study three isomeric natural polymers of glucose (polysaccharides), namely, cellulose, glycogen, and amylopectin (starch), having promising pharmaceutical applications, exceptional properties, and fascinating molecular structures. We intend to investigate and compute various closed-form formulas such as ABC, GA, sum-connectivity χ − 1 / 2, ABC 4, GA 5, and Sanskruti indices for the aforementioned macromolecules. Also, we present the closed-form formulas for the first, second, modified, and augmented Zagreb indices, inverse and general Randić indices, and symmetric division deg, harmonic, and inverse sum indices. Furthermore, we provide a comparative analysis using 3D graphs for these families of macromolecules to clarify their nature.