Rücker's walk count (WC) indices are well-known topological indices (TIs) used in Chemoinformatics to quantify the molecular structure of drugs represented by a graph in Quantitative structure-activity/property relationship (QSAR/QSPR) studies. In this work, we introduce for the first time the higher-order (kth order) analogues (WCk) of these indices using Markov chains. In addition, we report new QSPR models for large complex networks of different Bio-Systems useful in Parasitology and Neuroinformatics. The new type of QSPR models can be used for model checking to calculate numerical scores S(Lij) for links Lij (checking or re-evaluation of network connectivity) in large networks of all these fields. The method may be summarized as follows: (i) first, the WCk(j) values are calculated for all jth nodes in a complex network already created; (ii) A linear discriminant analysis (LDA) is used to seek a linear equation that discriminates connected or linked (Lij=1) pairs of nodes experimentally confirmed from non-linked ones (Lij=0); (iii) The new model is validated with external series of pairs of nodes; (iv) The equation obtained is used to re-evaluate the connectivity quality of the network, connecting/disconnecting nodes based on the quality scores calculated with the new connectivity function. The linear QSPR models obtained yielded the following results in terms of overall test accuracy for re-construction of complex networks of different Bio-Systems: parasite-host networks (93.14%), NW Spain fasciolosis spreading networks (71.42/70.18%) and CoCoMac Brain Cortex co-activation network (86.40%). Thus, this work can contribute to the computational re-evaluation or model checking of connectivity (collation) in complex systems of any science field.
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http://dx.doi.org/10.1016/j.biosystems.2013.02.006 | DOI Listing |
Environ Pollut
January 2025
School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing, 210094, China. Electronic address:
The soils/sediments organic carbon sorption coefficient (K) of organic substances is one of the indispensable environmental behavioral parameters in chemicals management. Because the test procedure used to measure K is normally expensive and time-consuming, predictive methods are considered vitally important technology to fill the data gap of K. In this study, quantitative structure-property relationship (QSPR) models are developed using a data set with 1477 experimental logK values and seven typical machine learning algorithms.
View Article and Find Full Text PDFHeliyon
January 2025
Department of Mathematics, Faculty of Sciences, Ghazi University, Dera Ghazi Khan, 32200, Pakistan.
Chemical structures may be defined based on their topology, which allows for the organization of molecules and the representation of new structures with specific properties. We use topological indices, which are precise numerical measurements independent of structure, to measure the bonding arrangement of a chemical network. An essential objective of studying topological indices is to collect and alter chemical structure data to develop a mathematical relationship between structures and physico-chemical properties, bio-activities, and associated experimental factors.
View Article and Find Full Text PDFSci Rep
January 2025
Department of Mathematical Sciences, Faculty of Science, Somali National University, Mogadishu Campus, Mogadishu, Somalia.
In recent years, machine learning has gained substantial attention for its ability to predict complex chemical and biological properties, including those of pharmaceutical compounds. This study proposes a machine learning-based quantitative structure-property relationship (QSPR) model for predicting the physicochemical properties of anti-arrhythmia drugs using topological descriptors. Anti-arrhythmic drug development is challenging due to the complex relationship between chemical structure and drug efficacy.
View Article and Find Full Text PDFMol Inform
January 2025
Department of Applied Chemistry, School of Science and Technology, Meiji University, 1-1-1 Higashi-Mita, Tama-ku, Kawasaki, Kanagawa 214-8571, Japan.
Recent advances in machine learning have significantly impacted molecular design, notably the molecular generation method combining the chemical variational autoencoder (VAE) with Gaussian mixture regression (GMR). In this method, a mathematical model is constructed with X as the latent variable of the molecule and Y as the target properties and activities. Through direct inverse analysis of this model, it is possible to generate molecules with the desired target properties.
View Article and Find Full Text PDFEnviron Pollut
January 2025
Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085, China.
Despite the significant benefits of aquatic passive sampling (low detection limits and time-weighted average concentrations), the use of passive samplers is impeded by uncertainties, particularly concerning the accuracy of sampling rates. This study employed a systematic evaluation approach based on the combination of meta-analysis and quantitative structure-property relationships (QSPR) models to address these issues. A comprehensive meta-analysis based on extensive data from 298 studies on the Polar Organic Chemical Integrative Sampler (POCIS) identified essential configuration parameters, including the receiving phase (type, mass) and the diffusion-limiting membrane (type, thickness, pore size), as key factors influencing uptake kinetic parameters.
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