Search results for "relationship"

showing 10 items of 3616 documents

Predicting antitrichomonal activity: A computational screening using atom-based bilinear indices and experimental proofs

2006

Existing Trichomonas vaginalis therapies are out of reach for most trichomoniasis people in developing countries and, where available, they are limited by their toxicity (mainly in pregnant women) and their cost. New antitrichomonal agents are needed to combat emerging metronidazole-resistant trichomoniasis and reduce the side effects associated with currently available drugs. Toward this end, atom-based bilinear indices, a new TOMOCOMD-CARDD molecular descriptor, and linear discriminant analysis (LDA) were used to discover novel, potent, and non-toxic lead trichomonacidal chemicals. Two discriminant functions were obtained with the use of non-stochastic and stochastic atom-type bilinear in…

Quantitative structure–activity relationshipDatabases FactualMolecular modelStereochemistryClinical BiochemistryDrug Evaluation PreclinicalPharmaceutical ScienceAntitrichomonal AgentsLigandsBiochemistryCross-validationChemometricsStructure-Activity Relationshipchemistry.chemical_compoundArtificial IntelligencePredictive Value of TestsMolecular descriptorDrug DiscoveryTrichomonas vaginalisAnimalsCluster AnalysisComputer SimulationMolecular BiologyStochastic ProcessesOrganic ChemistryComputational BiologyReproducibility of ResultsLinear discriminant analysisAntitrichomonal agentchemistryData Interpretation StatisticalTopological indexLinear ModelsMolecular MedicineBiological systemAlgorithmsBioorganic & Medicinal Chemistry
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Dragon method for finding novel tyrosinase inhibitors: Biosilico identification and experimental in vitro assays

2006

QSAR (quantitative structure-activity relationship) studies of tyrosinase inhibitors employing Dragon descriptors and linear discriminant analysis (LDA) are presented here. A data set of 653 compounds, 245 with tyrosinase inhibitory activity and 408 having other clinical uses were used. The active data set was processed by k-means cluster analysis in order to design training and prediction series. Seven LDA-based QSAR models were obtained. The discriminant functions applied showed a globally good classification of 99.79% for the best model Class=-96.067+1.988 x 10(2)X0Av +9 1.907 BIC3 + 6.853 CIC1 in the training set. External validation processes to assess the robustness and predictive pow…

Quantitative structure–activity relationshipDatabases FactualStereochemistryTyrosinaseQuantitative Structure-Activity RelationshipComputational biologyLigandsChemometricschemistry.chemical_compoundPiperidinesDrug DiscoveryComputer SimulationPharmacologyVirtual screeningbiologyChemistryOrganic ChemistryIn vitro toxicologyComputational BiologyDiscriminant AnalysisReproducibility of ResultsGeneral MedicineLinear discriminant analysisEnzyme inhibitorDrug Designbiology.proteinPeptidesKojic acidSoftwareEuropean Journal of Medicinal Chemistry
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Multi-target QSPR assemble of a Complex Network for the distribution of chemicals to biphasic systems and biological tissues

2008

Abstract Chemometrics, that based prediction on the probability of chemical distribution to different systems, is highly important for physicochemical, environmental, and life sciences. However, the amount of information is huge and difficult to analyze. A multi-system partition Complex Network (MSP-CN) may be very useful in this sense. We define MSP-CNs as large graphs composed by nodes (chemicals) interconnected by arcs if a pair of chemicals have similar partition in a given system. Experimental quantification of partition in many systems is expensive, so we can use a Quantitative Structure–Partition Relationship (QSPR) model. Unfortunately, with classic QSPR we need to use one model for…

Quantitative structure–activity relationshipDegree (graph theory)Markov chainChemistryProcess Chemistry and TechnologyComplex networkComputer Science ApplicationsAnalytical ChemistryPartition coefficientCombinatoricsChemometricsPartition (number theory)Node (circuits)Biological systemSpectroscopySoftwareChemometrics and Intelligent Laboratory Systems
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Molecular topology as a novel approach for drug discovery

2012

Molecular topology (MT) has emerged in recent years as a powerful approach for the in silico generation of new drugs. One key part of MT is that, in the process of drug design/discovery, there is no need for an explicit knowledge of a drug's mechanism of action unlike other drug discovery methods.In this review, the authors introduce the topic by explaining briefly the most common methodology used today in drug design/discovery and address the most important concepts of MT and the methodology followed (QSAR equations, LDA, etc.). Furthermore, the significant results achieved, from this approach, are outlined and discussed.The results outlined herein can be explained by considering that MT r…

Quantitative structure–activity relationshipDrug IndustryDrug discoveryProcess (engineering)Computer sciencebusiness.industryIn silicoQuantitative Structure-Activity RelationshipModels TheoreticalMachine learningcomputer.software_genreField (computer science)Pharmaceutical PreparationsDrug DesignDrug DiscoveryKey (cryptography)AnimalsComputer-Aided DesignHumansData miningArtificial intelligenceExplicit knowledgeMolecular topologybusinesscomputerExpert Opinion on Drug Discovery
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QSAR multi-target in drug discovery: a review.

2013

The main purpose of the present review is to summarize the most significant works up to date in the field of multi-target QSAR (mt-QSAR), in order to emphasize the importance that this technique has acquired over the last decade. Unlike traditional QSAR techniques, mt-QSAR permits to calculate the probability of activity of a given compound against different biological or pharmacological targets. In simple terms, a single equation for multiple outputs. To emphasize more the importance of the mt-QSAR in the field of drug discovery, we also present a novel mt-QSAR model, made on purpose by our research group, for the prediction of the susceptibility of Gram + and Gram - anaerobic bacteria.

Quantitative structure–activity relationshipDrug discoveryQuantitative Structure-Activity RelationshipGeneral MedicineComputational biologyBiologyBioinformaticsMulti targetDrug DiscoverySingle equationMolecular MedicineAnimalsHumansAnaerobic bacteriaMolecular Targeted TherapyAlgorithmsProbabilityCurrent computer-aided drug design
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Retrained Classification of Tyrosinase Inhibitors and “In Silico” Potency Estimation by Using Atom-Type Linear Indices

2012

In this paper, the authors present an effort to increase the applicability domain (AD) by means of retraining models using a database of 701 great dissimilar molecules presenting anti-tyrosinase activity and 728 drugs with other uses. Atom-based linear indices and best subset linear discriminant analysis (LDA) were used to develop individual classification models. Eighteen individual classification-based QSAR models for the tyrosinase inhibitory activity were obtained with global accuracy varying from 88.15-91.60% in the training set and values of Matthews correlation coefficients (C) varying from 0.76-0.82. The external validation set shows globally classifications above 85.99% and 0.72 fo…

Quantitative structure–activity relationshipEngineeringSpeedupbusiness.industryIn silicoAtom (order theory)Pattern recognitionLinear discriminant analysiscomputer.software_genreSet (abstract data type)Artificial intelligenceData miningbusinesscomputerSelection (genetic algorithm)Applicability domainInternational Journal of Chemoinformatics and Chemical Engineering
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Event-based criteria in GT-STAF information indices: theory, exploratory diversity analysis and QSPR applications

2012

Versatile event-based approaches for the definition of novel information theory-based indices (IFIs) are presented. An event in this context is the criterion followed in the "discovery" of molecular substructures, which in turn serve as basis for the construction of the generalized incidence and relations frequency matrices, Q and F, respectively. From the resultant F, Shannon's, mutual, conditional and joint entropy-based IFIs are computed. In previous reports, an event named connected subgraphs was presented. The present study is an extension of this notion, in which we introduce other events, namely: terminal paths, vertex path incidence, quantum subgraphs, walks of length k, Sach's subg…

Quantitative structure–activity relationshipEntropyChemistry OrganicInformation TheoryQuantitative Structure-Activity RelationshipBioengineeringInformation theoryJoint entropyMolecular descriptorDrug DiscoveryComputer GraphicsCluster AnalysisEntropy (information theory)QuantumMathematicsDiscrete mathematicsMolecular StructureLinear modelComputational BiologyGeneral MedicineEthylenesModels TheoreticalLinear ModelsMolecular MedicineSubstructureHydrophobic and Hydrophilic InteractionsAlgorithmsSoftwareSAR and QSAR in Environmental Research
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Prediction of acute toxicity of phenol derivatives using multiple linear regression approach for Tetrahymena pyriformis contaminant identification in…

2016

In this article, the modeling of inhibitory grown activity against Tetrahymena pyriformis is described. The 0-2D Dragon descriptors based on structural aspects to gain some knowledge of factors influencing aquatic toxicity are mainly used. Besides, it is done by some enlarged data of phenol derivatives described for the first time and composed of 358 chemicals. It overcomes the previous datasets with about one hundred compounds. Moreover, the results of the model evaluation by the parameters in the training, prediction and validation give adequate results comparable with those of the previous works. The more influential descriptors included in the model are: X3A, MWC02, MWC10 and piPC03 wit…

Quantitative structure–activity relationshipEnvironmental EngineeringDatabases FactualHealth Toxicology and Mutagenesis0211 other engineering and technologiesQuantitative Structure-Activity Relationship02 engineering and technology010501 environmental sciencesBiologycomputer.software_genre01 natural sciencesAquatic toxicologyPhenolsLinear regressionEnvironmental Chemistry0105 earth and related environmental sciences021110 strategic defence & security studiesDatabaseTetrahymena pyriformisPublic Health Environmental and Occupational HealthLinear modelGeneral MedicineGeneral ChemistryModels TheoreticalchEMBLPollutionAcute toxicityTetrahymena pyriformisLinear ModelscomputerChemical databaseChemosphere
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Predictive modeling of aryl hydrocarbon receptor (AhR) agonism

2020

Abstract The aryl hydrocarbon receptor (AhR) plays a key role in the regulation of gene expression in metabolic machinery and detoxification systems. In the recent years, this receptor has attracted interest as a therapeutic target for immunological, oncogenic and inflammatory conditions. In the present report, in silico and in vitro approaches were combined to study the activation of the AhR. To this end, a large database of chemical compounds with known AhR agonistic activity was employed to build 5 classifiers based on the Adaboost (AdB), Gradient Boosting (GB), Random Forest (RF), Multilayer Perceptron (MLP) and Support Vector Machine (SVM) algorithms, respectively. The built classifier…

Quantitative structure–activity relationshipEnvironmental EngineeringSupport Vector MachineHealth Toxicology and MutagenesisIn silico0208 environmental biotechnologyContext (language use)02 engineering and technologyComputational biology010501 environmental sciences01 natural scienceschemistry.chemical_compoundPhenolsBasic Helix-Loop-Helix Transcription FactorsEnvironmental ChemistryAnimalsHumans[CHIM]Chemical SciencesComputer SimulationBenzothiazolesProspective StudiesReceptorComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciencesRegulation of gene expressionbiologyChemistryPublic Health Environmental and Occupational HealthRobustness (evolution)General MedicineGeneral ChemistryAryl hydrocarbon receptorPollution020801 environmental engineering3. Good healthBenzothiazoleReceptors Aryl Hydrocarbonbiology.proteinNeural Networks Computer[INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM]Algorithms[CHIM.CHEM]Chemical Sciences/Cheminformatics
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A novel approach to predict aquatic toxicity from molecular structure

2008

The main aim of the study was to develop quantitative structure-activity relationship (QSAR) models for the prediction of aquatic toxicity using atom-based non-stochastic and stochastic linear indices. The used dataset consist of 392 benzene derivatives, separated into training and test sets, for which toxicity data to the ciliate Tetrahymena pyriformis were available. Using multiple linear regression, two statistically significant QSAR models were obtained with non-stochastic (R2=0.791 and s=0.344) and stochastic (R2=0.799 and s=0.343) linear indices. A leave-one-out (LOO) cross-validation procedure was carried out achieving values of q2=0.781 (scv=0.348) and q2=0.786 (scv=0.350), respecti…

Quantitative structure–activity relationshipEnvironmental EngineeringToxicity dataMolecular StructureLooHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryPollutionAquatic toxicologyToxicologyStructure-Activity RelationshipToxicity TestsBenzene derivativesTetrahymena pyriformisLinear regressionEnvironmental ChemistryBiological systemMathematicsChemosphere
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