Search results for "molecular topology"

showing 10 items of 58 documents

QSAR methods for the discovery of new inflammatory bowel disease drugs

2013

Inflammatory bowel disease (IBD) represents an important class of chronic gastrointestinal tract disease. And although there are already several useful treatments to reduce and control the symptoms, there is still no cure. One drug discovery technique used is the computer-aided (in silico) discovery approach which has largely demonstrated efficacy. Computational techniques, when used in combination with traditional drug discovery methodology, greatly increase the chance of drug discovery in a sustainable and economical fashion.This review aims to provide the most recent and important advances of in silico IBD drug discovery. While this review is mainly focused on QSAR methods, especially th…

Quantitative structure–activity relationshipCrohn's diseaseDrug discoverybusiness.industryIn silicoQuantitative Structure-Activity RelationshipDiseaseInflammatory Bowel Diseasesmedicine.diseaseBioinformaticsUlcerative colitisInflammatory bowel diseaseDrug DiscoverymedicineComputer-Aided DesignHumansMolecular topologybusinessExpert Opinion on Drug Discovery
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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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Molecular Topology QSAR Strategy for Crop Protection: New Natural Fungicides with Chitin Inhibitory Activity

2020

Nowadays, crop protection is a major concern and how to proceed is a delicate point of contention. New products must be safe and ecofriendly in accordance with the actual legislation. In this context, we present a quantitative structure-activity relationship strategy based on molecular topology as a tool for generating natural products as potential fungicides following a mechanism of action based on the synthesis of chitin inhibition (chitinase inhibition). Two discriminant equations using statistical linear discriminant analysis were used to identify three potential candidates (1-methylxanthine, hematommic acid, and antheraxanthin). The equations showed accuracy and specificity levels abov…

Quantitative structure–activity relationshipGeneral Chemical EngineeringGeneral ChemistryArticleNatural (archaeology)Crop protectionFungicidechemistry.chemical_compoundChemistryChitinchemistryBiochemical engineeringMolecular topologyQD1-999MathematicsACS Omega
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New hypoglycaemic agents selected by molecular topology.

2003

Abstract New compounds showing hypoglycaemic activity have been designed through a computer aided method based on quantitative structure–activity relationship (QSAR) and molecular connectivity. After calculation of topological indices for a set of 89 compounds including active and inactive with regards to hypoglycaemic action, linear discriminant analysis was performed so that a useful model to predict such an activity was achieved. Later on, the discriminant model was applied on a huge database so that fourteen compounds were selected as potential new hypoglycaemics. From them, just five were finally selected for experimental test on expected hypoglycaemic activity. Among the selected comp…

Quantitative structure–activity relationshipMolecular StructureDiscriminant modelPharmaceutical ScienceQuantitative Structure-Activity RelationshipPharmacologyLinear discriminant analysischemistry.chemical_compoundTolbutamidechemistryArabitolDrug DesignmedicinePotencyHypoglycemic AgentsMolecular topologymedicine.drugInternational journal of pharmaceutics
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Aplicación de la topología molecular a la predicción de la actividad antimalárica de análogos de la 4-anilinoquinolina

2021

La malaria es una enfermedad parasitaria causada por protozoos del género Plasmodium y transmitida por vectores del género Anopheles . En 2019 esta enfermedad se cobró la vida de más de 400.000 personas, de las cuales un 94 % se concentraban en la región de África. Uno de los principales problemas en el control de la malaria es la aparición de resistencias frente a los diferentes fármacos que existen, es por ello que es necesario el desarrollo de alternativas antimaláricas eficaces. En este estudio se ha aplicado la topología molecular a una serie de compuestos análogos de la 4-anilinoquinolina con actividad inhibitoria de la proliferación de 3 cepas de Plasmodium falciparum, una sensibl…

Quantitative structure–activity relationshipMolecular topologybiologyAnophelesTopología molecularPlasmodium falciparumbiology.organism_classificationmedicine.diseasePlasmodiumVirologyMalariaChloroquine3207 PatologíaParasitic diseasemedicineProtozoaMalariamedicine.drug
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Modeling Natural Anti-Inflammatory Compounds by Molecular Topology

2011

One of the main pharmacological problems today in the treatment of chronic inflammation diseases consists of the fact that anti-inflammatory drugs usually exhibit side effects. The natural products offer a great hope in the identification of bioactive lead compounds and their development into drugs for treating inflammatory diseases. Computer-aided drug design has proved to be a very useful tool for discovering new drugs and, specifically, Molecular Topology has become a good technique for such a goal. A topological-mathematical model, obtained by linear discriminant analysis, has been developed for the search of new anti-inflammatory natural compounds. An external validation obtained with …

Quantitative structure–activity relationshiplinear discriminant analysismedicine.drug_classAnti-Inflammatory AgentsQuantitative Structure-Activity RelationshipComputational biologyCatalysisAnti-inflammatoryNatural (archaeology)ArticleModel validationInorganic Chemistrylcsh:ChemistrymedicinePhysical and Theoretical ChemistryMolecular Biologylcsh:QH301-705.5Spectroscopynaturalanti-inflammatoryVirtual screeningBiological ProductsChemistryOrganic ChemistryExternal validationGeneral MedicineMolecular Topologyvirtual screeningCombinatorial chemistryComputer Science Applicationslcsh:Biology (General)lcsh:QD1-999Models ChemicalMolecular Topology; virtual screening; natural; anti-inflammatory; linear discriminant analysisIdentification (biology)Molecular topologyInternational Journal of Molecular Sciences
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Application of molecular topology to the prediction of antiparasitic activity against Giardia intestinalis and Trichomonas vaginalis of 2-Acylamino-n…

2020

Giardia intestinalis y Trichomonas vaginalis destacan por su importancia clínica. G. intestinalis causa la giardiosis, una parasitosis de gran importancia epidemiológica y clínica por presentar una elevada prevalencia. T. vaginalis causa la tricomoniasis, la enfermedad de transmisión sexual (ETS) no viral con mayor incidencia del mundo. Ambas parasitosis comparten el mismo tratamiento farmacológico: los nitroimidazoles. Se ha aplicado la topología molecular en la búsqueda de derivados del 2-Acylamino-nitro-1,3-tiazol con actividad antiparasitaria frente a G. intestinalis y T. vaginalis . Con el análisis lineal discriminante se obtuvo un modelo capaz de clasificar correctamente el 92,85 % de…

Sexually transmitted diseasePharmacologyHigh prevalenceMolecular topologyGiardiosisMolecular screeningTopología molecularBiologymedicine.disease_causeMolecular biologyPharmacological treatment2302.22 Farmacología MolecularFármacosmedicineTrichomonas vaginalisMultiple linear regression analysisParasitologíaParasitologyMolecular topology
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Molecular topology applied to the discovery of 1-benzyl-2-(3-fluorophenyl)-4-hydroxy-3-(3-phenylpropanoyl)-2H-pyrrole-5-one as a non-ligand-binding-p…

2014

We report the discovery of 1-benzyl-2-(3- fluorophenyl)-4-hydroxy-3-(3-phenylpropanoyl)-2H-pyrrole- 5-one as a novel non-ligand binding pocket (non-LBP) antagonist of the androgen receptor (AR) through the application of molecular topology techniques. This compound, validated through time-resolved fluorescence resonance energy transfer and fluorescence polarization biological assays, provides the basis for lead optimization and structure−activity relationship analysis of a new series of non-LBP AR antagonists. Induced-fit docking and molecular dynamics studies have been performed to establish a consistent hypothesis for the interaction of the new active molecule on the AR surface. Refereed/…

StereochemistryGeneral Chemical EngineeringMolecular ConformationLibrary and Information SciencesMolecular Dynamics Simulationmolecular topologySmall Molecule LibrariesMolecular dynamicschemistry.chemical_compoundStructure-Activity RelationshipUser-Computer Interfaceexperimental validationDrug DiscoveryFluorescence Resonance Energy TransferMoleculeHumansPyrrolesPyrroleBinding SitesChemistryAntagonistAndrogen AntagonistsGeneral Chemistryvirtual screeningComputer Science ApplicationsHigh-Throughput Screening AssaysAndrogen receptorMolecular Docking SimulationFörster resonance energy transferDocking (molecular)Receptors AndrogenThermodynamicsFluorescence anisotropyProtein Binding
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Prediction of Molecular Volume and Surface of Alkanes by Molecular Topology.

2003

Molecular volume and molecular surface are expressed as a function of topological degree in alkane graphs. This allows not only a straightforward approach to calculate such physicochemical magnitudes but also an interpretation of the role of the local vertex invariant (LOVI) or valence degree, delta, as well as the connectivity indices in the prediction of physicochemical properties. The interpretation is based on the concept of molecular accessibility (as introduced by Estrada, J. Phys. Chem. A 2002, 106, 9085) for which precise mathematical definitions are provided.

Vertex (graph theory)Surface (mathematics)Alkanechemistry.chemical_classificationValence (chemistry)Degree (graph theory)ChemistryGeometryGeneral ChemistryGeneral MedicineFunction (mathematics)Computer Science ApplicationsInterpretation (model theory)Computational Theory and MathematicsStatistical physicsMolecular topologyInvariant (mathematics)Information SystemsMathematicsChemInform
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Application of molecular topology to the prediction of inhibition of Trypanosoma cruzi Hexokinase by bisphosphonates

2008

Se ha desarrollado un modelo topológico-matemático para la búsqueda de nuevos derivados bisfosfonatos activos frente a la hexokinasa de Trypanosoma cruzi. Utilizando el análisis lineal discriminante se ha seleccionado una función con cuatro variables capaz de predecir adecuadamente la CI50 para cada compuesto de las series de entrenamiento y test. El modelo propuesto se ha aplicado a una librería molecular y se han propuesto nuevas estructuras potencialmente activas frente a T. cruzi.

Virtual screeningMolecular topologyLinear discriminant analysisTrypanosoma cruziHexokinaseLibrería molecularTopología molecularHexokinasaAnálisis lineal discriminante
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