Search results for "Biological system"

showing 10 items of 319 documents

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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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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Prediction of ionic liquid's heat capacity by means of their in silico principal properties

2016

The in silico principal properties (PPs) of ionic liquids (ILs), derived by means of the VolSurf+ approach, were used to develop a Partial Least Squares (PLS) model able to find a quantitative correlation among IL descriptors (accounting for both cationic and anionic structural features) and heat capacity values, providing affordable predictions validated by experimental Cp measurements for an external set of ILs. In silico predictions allowed the selection of a limited number of structurally different ILs with similar Cp values, providing the possibility to select an optimal IL according to efficiency, as well as to environmental and economic sustainability. The present general procedure, …

Quantitative structure–activity relationshipHeat capacity010405 organic chemistryGeneral Chemical EngineeringIn silicoPrincipal (computer security)Chemistry (all)General ChemistrySettore CHIM/06 - Chimica Organica010402 general chemistry01 natural sciencesHeat capacityQuantitative correlation0104 chemical sciencesIonic liquidschemistry.chemical_compoundEconomic sustainabilitychemistryIonic liquids; QSPR; Heat capacityQSPRPartial least squares regressionIonic liquidChemical Engineering (all)Biological systemMathematics
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Unified Markov thermodynamics based on stochastic forms to classify drugs considering molecular structure, partition system, and biological species:

2005

Abstract To date, molecular descriptors do not commonly account for important information beyond chemical structure. The present work, attempts to extend, in this sense, the stochastic molecular descriptors (Gonzalez-Diaz, H. et al., J. Mol. Mod. 2002, 8, 237), incorporating information about the specific biphasic partition system, the biological species, and chemical structure inside the molecular descriptors. Consequently, MARCH-INSIDE molecular descriptors may be identified with time-dependent thermodynamic parameters (entropy and mean free energy) of partition process. A classification function was developed to classify data of 423 drugs and up to 14 different partition systems at the s…

Quantitative structure–activity relationshipMolecular modelMarkov chainChemistryStereochemistryOrganic ChemistryClinical BiochemistryPharmaceutical ScienceWiener indexMarkov modelBiochemistryPartition coefficientMolecular descriptorDrug DiscoveryMolecular MedicineBiological systemMolecular BiologyAntibacterial agentBioorganic & Medicinal Chemistry Letters
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New tyrosinase inhibitors selected by atomic linear indices-based classification models.

2005

In the present report, the use of the atom-based linear indices for finding functions that discriminate between the tyrosinase inhibitor compounds and inactive ones is presented. In this sense, discriminant models were applied and globally good classifications of 93.51% and 92.46% were observed for non-stochastic and stochastic linear indices best models, respectively, in the training set. The external prediction sets had accuracies of 91.67% and 89.44%. In addition, these fitted models were used in the screening of new cycloartane compounds isolated from herbal plants. A good behavior is shown between the theoretical and experimental results. These results provide a tool that can be used i…

Quantitative structure–activity relationshipMolecular modelStereochemistryTyrosinaseClinical BiochemistryMolecular ConformationPharmaceutical ScienceQuantitative Structure-Activity RelationshipBiochemistrySensitivity and SpecificityChemometricsDrug DiscoveryComputer SimulationEnzyme InhibitorsMolecular BiologyTraining setChemistryMonophenol MonooxygenaseOrganic ChemistryLinear discriminant analysisTriterpenesDiscriminantModels ChemicalTopological indexMolecular MedicineBiological systemBioorganicmedicinal chemistry letters
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tomocomd-camps and protein bilinear indices - novel bio-macromolecular descriptors for protein research: I. Predicting protein stability effects of a…

2010

Descriptors calculated from a specific representation scheme encode only one part of the chemical information. For this reason, there is a need to construct novel graphical representations of proteins and novel protein descriptors that can provide new information about the structure of proteins. Here, a new set of protein descriptors based on computation of bilinear maps is presented. This novel approach to biomacromolecular design is relevant for QSPR studies on proteins. Protein bilinear indices are calculated from the kth power of nonstochastic and stochastic graph–theoretic electronic-contact matrices, and , respectively. That is to say, the kth nonstochastic and stochastic protein bili…

Quantitative structure–activity relationshipProtein structureLinear regressionStability (learning theory)Bilinear interpolationCell BiologySegmented regressionRepresentation (mathematics)Linear discriminant analysisBiological systemMolecular BiologyBiochemistryMathematicsFEBS Journal
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Atom-Based Quadratic Indices to Predict Aquatic Toxicity of Benzene Derivatives to <i>Tetrahymena pyriformis</i>

2009

The non-stochastic and stochastic atom-based quadratic indices are applied to develop quantitative structure-activity relationship (QSAR) models for the prediction of aquatic toxicity. The used dataset, consisting of 392 benzene derivatives for which toxicity data to the ciliate Tetrahymena pyriformis were available, is divided into training and test sets. The obtained multiple linear regression models are statistically significant (R2 = 0.787 and s = 0.347, R2 = 0.806 and s = 0.329, for non-stochastic and stochastic quadratic indices, respectively) and show rather good stability in a cross-validation experiment (q2 = 0.769 and scv = 0.357, q2 = 0.791 and scv = 0.337, correspondingly). In a…

Quantitative structure–activity relationshipQuadratic equationTest setToxicityLinear regressionTetrahymena pyriformisBiological systemStability (probability)MathematicsAquatic toxicologyProceedings of The 13th International Electronic Conference on Synthetic Organic Chemistry
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Bond-based bilinear indices for computational discovery of novel trypanosomicidal drug-like compounds through virtual screening

2014

Two-dimensional bond-based bilinear indices and linear discriminant analysis are used in this report to perform a quantitative structure-activity relationship study to identify new trypanosomicidal compounds. A data set of 440 organic chemicals, 143 with antitrypanosomal activity and 297 having other clinical uses, is used to develop the theoretical models. Two discriminant models, computed using bond-based bilinear indices, are developed and both show accuracies higher than 86% for training and test sets. The stochastic model correctly indentifies nine out of eleven compounds of a set of organic chemicals obtained from our synthetic collaborators. The in vitro antitrypanosomal activity of …

Quantitative structure–activity relationshipStereochemistryTrypanosoma cruziDrug Evaluation PreclinicalQuantitative Structure-Activity RelationshipBilinear interpolationSet (abstract data type)MiceDrug DiscoveryIc50 valuesmedicineAnimalsCells CulturedPharmacologyStochastic ProcessesVirtual screeningDose-Response Relationship DrugMolecular StructureChemistryMacrophagesOrganic ChemistryDiscriminant AnalysisGeneral MedicineLinear discriminant analysisTrypanocidal AgentsDiscriminantBenznidazoleBiological systemmedicine.drugEuropean Journal of Medicinal Chemistry
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Atom, atom-type, and total nonstochastic and stochastic quadratic fingerprints: a promising approach for modeling of antibacterial activity.

2005

The TOpological MOlecular COMputer Design (TOMOCOMD-CARDD) approach has been introduced for the classification and design of antimicrobial agents using computer-aided molecular design. For this propose, atom, atom-type, and total quadratic indices have been generalized to codify chemical structure information. In this sense, stochastic quadratic indices have been introduced for the description of the molecular structure. These stochastic fingerprints are based on a simple model for the intramolecular movement of all valence-bond electrons. In this work, a complete data set containing 1006 antimicrobial agents is collected and presented. Two structure-based antibacterial activity classificat…

Quantitative structure–activity relationshipStochastic ProcessesMolecular modelDatabases FactualChemistryOrganic ChemistryClinical BiochemistryMolecular ConformationPharmaceutical ScienceAtom (order theory)Quantitative Structure-Activity RelationshipModels TheoreticalLinear discriminant analysisBiochemistryAnti-Bacterial AgentsSet (abstract data type)Quadratic equationSimple (abstract algebra)Drug DiscoveryMolecular MedicineComputer SimulationBiological systemMolecular BiologyAntibacterial agentBioorganicmedicinal chemistry
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Prediction of potential environmental toxicity of chemicals in <em>Lactuca sativa</em> seed germination using computational tools

2019

The main aim of the study was to develop quantitative structure-activity relationship (QSAR) models for the prediction of phytotoxicity effects of chemical compounds on the Lactuca sativa seeds germination. A database of 73 compounds, assayed against L. sativa and Dragon’s molecular descriptors are used to obtain a QSAR model for the prediction of the phytotoxicity. The model is carried out with QSARINS software and validated according to OECD principles. The best model showed good value for the determination coefficient (R2 = 0.917) and others parameters appropriate for fitting (s = 0.256 and RMSEtr= 0.236). The validation results confirmed that the model has good robustness and stability …

Quantitative structure–activity relationshipbiologyGerminationMolecular descriptorEnvironmental toxicologyPhytotoxicityLactucaBiological systembiology.organism_classificationMathematicsProceedings of MOL2NET 2019, International Conference on Multidisciplinary Sciences, 5th edition
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