Search results for "quantitative"

showing 10 items of 2409 documents

Determination of Magnesium in Fertilizers by Inductively Coupled Plasma Atomic Emission Spectrometry: Studies of Some Spectral and Interelement Effec…

1995

Abstract Four analytical wavelengths of magnesium were tested for determination of Mg from fertilizers by inductively coupled plasma atomic emission spectroscopy (ICP-AES): 202.528, 285.213, and 383.826 nm (Mg I) and 279.553 (Mg II). The effects of fertilizer matrix elements on Mg determination were examined by adding matrix elements to fertilizer solutions. Multiple linear regression calculations proved a valuable technique for evaluating the effects of matrix elements on Mg determination. The observed interferences at Mg wavelengths may be both spectral and interelement. Interelement effects were typically caused by Na, K, and Ca, and spectral effects, by P, Fe, and S. The best wavelength…

PharmacologyMagnesiumAnalytical chemistrychemistry.chemical_elementAnalytical ChemistryMatrix (chemical analysis)WavelengthchemistryInductively coupled plasma atomic emission spectroscopyEnvironmental ChemistryInductively coupled plasmaOptical emission spectrometryAgronomy and Crop ScienceQuantitative analysis (chemistry)Food ScienceAtomic emission spectrometryJournal of AOAC INTERNATIONAL
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Prediction of tyrosinase inhibition activity using atom-based bilinear indices.

2007

A set of novel atom-based molecular fingerprints is proposed based on a bilinear map similar to that defined in linear algebra. These molecular descriptors (MDs) are proposed as a new means of molecular parametrization easily calculated from 2D molecular information. The nonstochastic and stochastic molecular indices match molecular structure provided by molecular topology by using the kth nonstochastic and stochastic graph-theoretical electronic-density matrices, M(k) and S(k), respectively. Thus, the kth nonstochastic and stochastic bilinear indices are calculated using M(k) and S(k) as matrix operators of bilinear transformations. Chemical information is coded by using different pair com…

PharmacologyMelaninsQuantitative structure–activity relationshipStochastic ProcessesSeries (mathematics)Molecular StructureChemistryMonophenol MonooxygenaseOrganic ChemistryBilinear interpolationLinear discriminant analysisBiochemistryStructure-Activity RelationshipDiscriminantModels ChemicalComputational chemistryMolecular descriptorDrug DiscoveryLinear algebraMolecular MedicineComputer SimulationGeneral Pharmacology Toxicology and PharmaceuticsBilinear mapEnzyme InhibitorsBiological systemChemMedChem
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New agents active against Mycobacterium avium complex selected by molecular topology: a virtual screening method

2003

Objectives: In order to select new drugs and to predict their in vitro activity against Mycobacterium avium complex (MAC), new quantitative structure-activity relationship (QSAR) models were developed. Methods: The activities against MAC of 29 structurally heterogeneous drugs were examined by means of linear discriminant analysis (LDA) and multilinear regression analysis (MLRA) by using topological indices (TI) as structural descriptors. In vitro antimycobacterial activities were determined by a broth microdilution method with 7H9 medium. Results: The topological model obtained successfully classifies over 80% of compounds as active or inactive; consequently, it was applied in the search fo…

PharmacologyMicrobiology (medical)Virtual screeningQuantitative structure–activity relationshipbiologymedicine.drug_classBroth microdilutionQuantitative Structure-Activity RelationshipMicrobial Sensitivity TestsComputational biologyMycobacterium avium Complexbiology.organism_classificationLinear discriminant analysisAntimycobacterialModels BiologicalIn vitroAnti-Bacterial AgentsMicrobiologyInfectious DiseasesDrug DesignmedicinePharmacology (medical)Mycobacterium avium complexMolecular topologyJournal of Antimicrobial Chemotherapy
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3D-QSAR pharmacophore modeling and in silico screening of new Bcl-xl inhibitors.

2010

Bcl-2 proteins family members play several roles in tumoral proliferation: they inhibit proapoptotic activity during oncogenesis, support tumor cells survival, induce chemoresistance. The discovery of new small inhibitors of Bcl-xl represents a new frontier for cancer treatment. In this study, a 3D-QSAR pharmacophore model was developed, based on 42 biarylacylsulfonamides, and used to understand the structural factors affecting the inhibitory potency of these derivatives. Aromatic, negative charge, and hydrogen bond acceptor effects contribute to the inhibitory activity. The model was then employed as 3D search query to screen ZINC drug-like database in order to select new scaffolds. Finall…

PharmacologyModels MolecularVirtual screeningQuantitative structure–activity relationshipTertiary amineMolecular modelChemistryIn silicoOrganic ChemistryMolecular Conformationbcl-X ProteinQuantitative Structure-Activity RelationshipGeneral MedicineSettore CHIM/08 - Chimica FarmaceuticaBiochemistryIn vivoDocking (molecular)Drug Discovery3D-QSAR Pharmacophore Modeling In Silico Screening Bcl-xl InhibitorsPharmacophoreEuropean journal of medicinal chemistry
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A topological sub-structural approach for predicting human intestinal absorption of drugs.

2004

The human intestinal absorption (HIA) of drugs was studied using a topological sub-structural approach (TOPS-MODE). The drugs were divided into three classes according to reported cutoff values for HIA. "Poor" absorption was defined as HIAor =30%, "high" absorption as HIAor =80%, whereas "moderate" absorption was defined between these two values (30%HIA79%). Two linear discriminant analyses were carried out on a training set of 82 compounds. The percentages of correct classification, for both models, were 89.02%. The predictive power of the models were validated by three test: a leave-one-out cross validation procedure (88.9% and 87.9%), an external prediction set of 127 drugs (92.9% and 80…

PharmacologyQuantitative structure–activity relationshipChemistryOrganic ChemistryBiological AvailabilityQuantitative Structure-Activity RelationshipGeneral MedicineModels TheoreticalLinear discriminant analysisTopologyCross-validationIntestinal absorptionBioavailabilityIntestinal AbsorptionPharmaceutical PreparationsTest setDrug DiscoveryHuman intestinal absorptionCutoffHumansIntestinal MucosaEuropean journal of medicinal chemistry
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Prediction of Aquatic Toxicity of Benzene Derivatives to Tetrahymena pyriformis According to OECD Principles

2016

Background: Many QSAR studies have been developed to predict acute toxicity over several biomarkers like Pimephales promelas, Daphnia magna and Tetrahymena pyriformis. Regardless of the progress made in this field there are still some gaps to be resolved such as the prediction of aquatic toxicity over the protozoan T. pyriformis still lack a QSAR study focused in accomplish the OECD principles. Methods: Atom-based quadratic indices are used to obtain quantitative structure-activity relationship (QSAR) models for the prediction of aquatic toxicity. Our models agree with the principles required by the OECD for QSAR models to regulatory purposes. The database employed consists of 392 substitut…

PharmacologyQuantitative structure–activity relationshipTetrahymena pyriformisAntiprotozoal AgentsQuantitative Structure-Activity Relationship010501 environmental sciencesBiology01 natural sciencesAcute toxicity0104 chemical sciencesAquatic toxicologyToxicology010404 medicinal & biomolecular chemistryParasitic Sensitivity TestsTest setDrug DiscoveryBenzene derivativesLinear regressionTetrahymena pyriformisBenzene DerivativesBiological systemMonte Carlo MethodAlgorithmsBootstrapping (statistics)0105 earth and related environmental sciencesCurrent Pharmaceutical Design
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New Hypolipaemic Agents Designed by Molecular Topology: Pharmacological Studies of 2,6-Di-tert-butyl-4-methylpyridine and 2,6-Di-tert-butylpyridine

1999

New compounds showing hypolipaemic activity have been designed using a computer-aided method based on molecular topology and QSAR analysis. Linear discriminant analysis and connectivity functions were used to design three potentially suitable drugs which were tested for hypolipaemic properties by the Triton WR-1339 test in rats. The pharmacological tests carried out on the newly designed compounds demonstrated the existence of notable activity in phase I for two of them. namely 2,6-Di-tert-butyl-4-methylpyridine (C.A.S. 38222-83-2) and 2,6-Di-tert-butylpyridine (C.A.S. 585-48-8), with respect to the level of total cholesterol. Both substances decrease the lipaemia to lower levels than clofi…

PharmacologyTert butylQuantitative structure–activity relationshipClofibrateChemistryStereochemistry26-Di-tert-butylpyridineReference drugchemistry.chemical_compoundTotal cholesterol4-MethylpyridinemedicineMolecular topologymedicine.drugQuantitative Structure-Activity Relationships
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Introduction to molecular topology: basic concepts and application to drug design.

2012

In this review it is dealt the use of molecular topology (MT) in the selection and design of new drugs. After an introduction of the actual methods used for drug design, the basic concepts of MT are defined, including examples of calculation of topological indices, which are numerical descriptors of molecular structures. The goal is making this calculation familiar to the potential students and allowing a straightforward comprehension of the topic. Finally, the achievements obtained in this field are detailed, so that the reader can figure out the great interest of this approach.

PharmacologyTheoretical computer scienceMolecular Structurebusiness.industryComputer scienceQuantitative Structure-Activity RelationshipGeneral Medicinecomputer.software_genreField (computer science)ComprehensionPharmaceutical PreparationsDrug DesignDrug DiscoveryNumerical descriptorsSelection (linguistics)Molecular MedicineComputer Aided DesignAnimalsComputer-Aided DesignHumansArtificial intelligenceMolecular topologybusinesscomputerCurrent computer-aided drug design
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Bond-Based 2D Quadratic Fingerprints in QSAR Studies: Virtual and In vitro Tyrosinase Inhibitory Activity Elucidation

2010

In this report, we show the results of quantitative structure–activity relationship (QSAR) studies of tyrosinase inhibitory activity, by using the bond-based quadratic indices as molecular descriptors (MDs) and linear discriminant analysis (LDA), to generate discriminant functions to predict the anti-tyrosinase activity. The best two models [Eqs (6) and (12)] out of the total 12 QSAR models developed here show accuracies of 93.51% and 91.21%, as well as high Matthews correlation coefficients (C) of 0.86 and 0.82, respectively, in the training set. The validation external series depicts values of 90.00% and 89.44% for these best two equations (6) and (12), respectively. Afterwards, a second …

PharmacologyVirtual screeningQuantitative structure–activity relationshipChemistryStereochemistryTyrosinaseOrganic ChemistryLinear discriminant analysisBiochemistrychemistry.chemical_compoundQuadratic equationDiscriminantMolecular descriptorDrug DiscoveryMolecular MedicineKojic acidChemical Biology & Drug Design
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Intraspezifische Unterschiede der relativen Hirngrösse beim Löwen (Panthera leo L.)

1971

Different stages of brain evolution expressed by the allometric relation of3√ brain capacity and basal length of the skull are shown to be existent in the speciesPanthera leo. Whereas Asiatic lions obviously have the same level of brain size as leopards (Panthera pardus), African lions have higher brain capacities. A third level seems to be represented by the upper pleistocene American lion,Panthera leo atrox. These results permit us to reject some conceptions ofHerre andRohrs13 concerning the quantitative expression of mammalian brain evolution.

PharmacologybiologyEcologyZoologyCell Biologybiology.organism_classificationMammalian brainCellular and Molecular Neurosciencebiology.animalAmerican lionBrain sizeMolecular MedicineQuantitative expressionAllometryPantheraMolecular BiologyExperientia
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