Few variables were selected from a pool of calculated Dragon descriptors through three different feature selection methods, namely genetic algorithm (GA), successive projections algorithm (SPA), and fuzzy rough set ant colony optimization (fuzzy rough set ACO). Each set of selected descriptors was regressed against the bioactivities of a series of glycogen synthase kinase-3β (GSK-3β) inhibitors, through linear and nonlinear regression methods, namely multiple linear regression (MLR), artificial neural network (ANN), and support vector machines (SVM). The fuzzy rough set ACO/SVM-based model gave the best estimation/prediction results, demonstrating the nonlinear nature of this analysis and suggesting fuzzy rough set ACO, first introduced in ...
Background: Alzheimer's disease affects a large part of the world's population by prolonging the hum...
The discovery of selective inhibitors of biological target proteins is the primary goal of many drug...
G protein-coupled receptors (GPCRs) play an essential role in critical human activities, and they ar...
Few variables were selected from a pool of calculated Dragon descriptors through three different fea...
In cancer chemotherapy, multidrug resistance (MDR) is a major clinical problem which occurs by an in...
Aromatase inhibition is an effective treatment strategy for breast cancer. Currently, several in sil...
Quantitative structure-activity relationship (QSAR) models are mathematical equations constructing a...
Glycogen synthase kinase-3 (GSK-3) is a multifunctional serine/threonine protein kinase which is eng...
<div><p>Linear and non-linear quantitative structure-activity relationship (QSAR) models were presen...
AbstractCombinations of multiple linear regressions, genetic algorithms and artificial neural networ...
The Cyclin-Dependent Kinases (CDKs) are the core components coordinating eukaryotic cell division cy...
AbstractIn this work, the quantitative structure–activity relationship models were developed for pre...
Caballero, J (Caballero, Julio). Univ Talca, Ctr Bioinformat & Simulac Mol, Talca, ChileMany article...
A quantitative structure–activity relationship (QSAR) modeling was carried out for the anti-HIV-1 ac...
In silico screening of chemical libraries or virtual chemicals may reduce drug discovery and medicin...
Background: Alzheimer's disease affects a large part of the world's population by prolonging the hum...
The discovery of selective inhibitors of biological target proteins is the primary goal of many drug...
G protein-coupled receptors (GPCRs) play an essential role in critical human activities, and they ar...
Few variables were selected from a pool of calculated Dragon descriptors through three different fea...
In cancer chemotherapy, multidrug resistance (MDR) is a major clinical problem which occurs by an in...
Aromatase inhibition is an effective treatment strategy for breast cancer. Currently, several in sil...
Quantitative structure-activity relationship (QSAR) models are mathematical equations constructing a...
Glycogen synthase kinase-3 (GSK-3) is a multifunctional serine/threonine protein kinase which is eng...
<div><p>Linear and non-linear quantitative structure-activity relationship (QSAR) models were presen...
AbstractCombinations of multiple linear regressions, genetic algorithms and artificial neural networ...
The Cyclin-Dependent Kinases (CDKs) are the core components coordinating eukaryotic cell division cy...
AbstractIn this work, the quantitative structure–activity relationship models were developed for pre...
Caballero, J (Caballero, Julio). Univ Talca, Ctr Bioinformat & Simulac Mol, Talca, ChileMany article...
A quantitative structure–activity relationship (QSAR) modeling was carried out for the anti-HIV-1 ac...
In silico screening of chemical libraries or virtual chemicals may reduce drug discovery and medicin...
Background: Alzheimer's disease affects a large part of the world's population by prolonging the hum...
The discovery of selective inhibitors of biological target proteins is the primary goal of many drug...
G protein-coupled receptors (GPCRs) play an essential role in critical human activities, and they ar...