Search results for "ADME"

showing 10 items of 22 documents

In silico methods for metabolomic and toxicity prediction of zearalenone, α-zearalenone and β-zearalenone.

2020

Zearalenone (ZEA), α-zearalenol (α-ZEL) and β-zearalenol (β-ZEL) (ZEA's metabolites) are co/present in cereals, fruits or their products. All three with other compounds, constitute a cocktail-mixture that consumers (and also animals) are exposed and never entirely evaluated, nor in vitro nor in vivo. Effect of ZEA has been correlated to endocrine disruptor alterations as well as its metabolites (α-ZEL and β-ZEL); however, toxic effects associated to metabolites generated once ingested are unknown and difficult to study. The present study defines the metabolomics profile of all three mycotoxins (ZEA, α-ZEL and β-ZEL) and explores the prediction of their toxic effects proposing an in silico w…

In silicoMetaboliteToxicologyArticleAmes test03 medical and health scienceschemistry.chemical_compound0404 agricultural biotechnologyMetabolomicsGlucuronidesCytochrome P-450 Enzyme SystemIn vivoAnimalsMetabolomicsComputer SimulationMycotoxinZearalenoneZebrafish030304 developmental biology0303 health sciencesChemistryIn silicofood and beverages04 agricultural and veterinary sciencesGeneral Medicine040401 food sciencePASS onlineEndocrine disruptorBiochemistryBlood-Brain BarrierMetaToxZearalenoneSwissADMEReactive Oxygen SpeciesPredictionFood ScienceFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association
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Pharmacokinetics in Drug Discovery

2007

The aim of this current review is to summarize the present status of pharmacokinetics in Drug Discovery. The review is structured into four sections. The first section is a general overview of what we understand by pharmacokinetics and the different LADMET aspects: Liberation, Absorption, Distribution, Metabolism, Excretion, and Toxicity. The second section highlights the different computational or in silico approaches to estimate/predict one or several aspects of the pharmacokinetic profile of a discovery lead compound. The third section discusses the most commonly used in vitro methodologies. The fourth and last section examines the various approaches employed towards the pharmacokinetic …

Models MolecularProteomicsDrug discoverybusiness.industryManagement scienceComputer aidPharmaceutical ScienceGenomicsPopulation pharmacokineticsPharmacologyModels BiologicalPharmacokineticsPharmaceutical technologyDrug DesignMajor conclusionAnimalsHumansMedicinePharmacokineticsbusinessProtein BindingADMEJournal of Pharmaceutical Sciences
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The discovery of novel antitrypanosomal 4-phenyl-6-(pyridin-3-yl)pyrimidines

2021

Human African trypanosomiasis, or sleeping sickness, is a neglected tropical disease caused by Trypanosoma brucei rhodesiense and Trypanosoma brucei gambiense which seriously affects human health in Africa. Current therapies present limitations in their application, parasite resistance, or require further clinical investigation for wider use. Our work herein describes the design and syntheses of novel antitrypanosomal 4-phenyl-6-(pyridin-3-yl)pyrimidines, with compound 13, the 4-(2-methoxyphenyl)-6-(pyridine-3-yl)pyrimidin-2-amine demonstrating an IC50 value of 0.38 μM and a promising off-target ADME-Tox profile in vitro. In silico molecular target investigations showed rhodesain to be a pu…

Models MolecularTrypanosoma brucei rhodesiensepyrimidinessleeping sicknessIn silicoHuman african trypanosomiasis01 natural sciencesDockingCell Line03 medical and health sciencesantitrypanosomalDrug DiscoverymedicineAnimalsHumansAfrican trypanosomiasisIC50030304 developmental biologyrhodesainPharmacology0303 health sciences010405 organic chemistryChemistryDrug discoveryOrganic ChemistryAntitrypanosomalSleeping sicknessTrypanosoma brucei rhodesienseGeneral MedicineHuman African Trypanosomiasismedicine.diseaseTrypanocidal AgentsIn vitroRats0104 chemical sciencesPyrimidinesRhodesainTrypanosomiasis AfricanBiochemistryDrug developmentDocking (molecular)dockingADME-ToxResearch Paper
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Imaginary time propagation code for large-scale two-dimensional eigenvalue problems in magnetic fields

2013

We present a code for solving the single-particle, time-independent Schr\"odinger equation in two dimensions. Our program utilizes the imaginary time propagation (ITP) algorithm, and it includes the most recent developments in the ITP method: the arbitrary order operator factorization and the exact inclusion of a (possibly very strong) magnetic field. Our program is able to solve thousands of eigenstates of a two-dimensional quantum system in reasonable time with commonly available hardware. The main motivation behind our work is to allow the study of highly excited states and energy spectra of two-dimensional quantum dots and billiard systems with a single versatile code, e.g., in quantum …

NetlibSource codeta114Computer sciencemedia_common.quotation_subjectFOS: Physical sciencesGeneral Physics and AstronomyByteComputational Physics (physics.comp-ph)Python (programming language)computer.software_genreImaginary timeComputational scienceHardware and ArchitectureREADMECompilerPhysics - Computational PhysicscomputerAlgorithmmedia_commonTest datacomputer.programming_languageComputer Physics Communications
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Precision-cut liver slices: A tool to model the liver ex vivo

2013

D is ea se Precision-cut liver slices: A tool to model the liver ex vivo Peter Olinga1,2,*, Detlef Schuppan2 1Division of Pharmaceutical Technology and Biopharmacy, Departement of Pharmacy, University of Groningen, The Netherlands; 2Molecular and Translational Medicine, Department of Medicine I, University Medical Center, Johannes Gutenberg University Mainz, Germany *Corresponding author. Address: Division of Pharmaceutical Technology and Biopharmacy, Departement of Pharmacy, University of Groningen, The Netherlands. Tel.: + 31 50 363 8373; fax: +31 50 363 2500. *E-mail address: P.Olinga@rug.nl

Organ Culture TechniqueLiver slicesmedicine.medical_specialtyHepatologybusiness.industryDisease modelPharmacyGastroenterologyFibrosisRatsEx vivoFibrogenesisMiceOrgan Culture TechniquesADMETPharmaceutical technologyLiverInternal medicineMedicineAnimalsHumansUniversity medicalMedical physicsbusinessEx vivoJournal of Hepatology
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Predicting and Tuning Physicochemical Properties in Lead Optimization: Amine Basicities

2007

This review describes simple and useful concepts for predicting and tuning the pK(a) values of basic amine centers, a crucial step in the optimization of physical and ADME properties of many lead structures in drug-discovery research. The article starts with a case study of tricyclic thrombin inhibitors featuring a tertiary amine center with pK(a) values that can be tuned over a wide range, from the usual value of around 10 to below 2 by (remote) neighboring functionalities commonly encountered in medicinal chemistry. Next, the changes in pK(a) of acyclic and cyclic amines upon substitution by fluorine, oxygen, nitrogen, and sulfur functionalities, as well as carbonyl and carboxyl derivativ…

PharmacologyTertiary amineChemistryChemistry PharmaceuticalOrganic ChemistryInformation Storage and Retrievalchemistry.chemical_elementBiochemistryAntithrombinsAmine ligandsComputational chemistryDrug DesignOrganocatalysisDrug DiscoveryFluorineMolecular MedicineOrganic chemistryAmine gas treatingAminesGeneral Pharmacology Toxicology and PharmaceuticsCyclic aminesADMEChemMedChem
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The Use of Rule-Based and QSPR Approaches in ADME Profiling: A Case Study on Caco-2 Permeability.

2013

During the early ADME profiling the development of simple, interpretable and reliable in silico tools is very important. In this study, rule-based and QSPR approaches were investigated using a large Caco-2 permeability database. Three permeability classes were determined: high (H), moderate (M) and low (L). The main physicochemical properties related with permeability were ranked as follows: Polar Surface Area (PSA)>Lipophilicity (logP/logD)>Molecular Weight (MW)>number of Hydrogen Bond donors and acceptors>Ionization State>number of Rotatable Bonds>number of Rings. The best rule, based on the combination of PSA-MW-logD (3PRule), was able to identify the H, M and L classes with accuracy of …

Profiling (computer programming)Quantitative structure–activity relationshipChemistryOrganic ChemistryRule-based systemCombinatorial chemistryComputer Science ApplicationsPolar surface areaBinary classificationStructural BiologyTest setDrug DiscoveryLipophilicityMolecular MedicineBiological systemADMEMolecular informatics
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Quantitative Structure-Antioxidant Activity Models of Isoflavonoids: A Theoretical Study

2015

Seventeen isoflavonoids from isoflavone, isoflavanone and isoflavan classes are selected from Dalbergia parviflora. The ChEMBL database is representative from these molecules, most of which result highly drug-like. Binary rules appear risky for the selection of compounds with high antioxidant capacity in complementary xanthine/xanthine oxidase, ORAC, and DPPH model assays. Isoflavonoid structure-activity analysis shows the most important properties (log P, log D, pKa, QED, PSA, NH + OH ≈ HBD, N + O ≈ HBA). Some descriptors (PSA, HBD) are detected as more important than others (size measure Mw, HBA). Linear and nonlinear models of antioxidant potency are obtained. Weak nonlinear relationship…

Quantitative structure–activity relationshipAntioxidantantioxidantStereochemistryDPPHDalbergiamedicine.medical_treatmentQuantitative Structure-Activity RelationshipFlavonesArticleAntioxidantsCatalysisInorganic Chemistrylcsh:Chemistrychemistry.chemical_compoundIsoflavonoidmedicineStructure–activity relationshipPhysical and Theoretical ChemistryXanthine oxidaseMolecular Biologylcsh:QH301-705.5Spectroscopychemistry.chemical_classificationChemistryQSARstructure-activity relationshippoor absorption or permeationOrganic ChemistryGeneral MedicineIsoflavonesIsoflavonesComputer Science ApplicationsADMETBiochemistrylcsh:Biology (General)lcsh:QD1-999Oxidation-ReductionabsorptionInternational Journal of Molecular Sciences
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Modeling of interactions between xenobiotics and cytochrome P450 (CYP) enzymes

2015

The adverse effects to humans and environment of only few chemicals are well known. Absorption, distribution, metabolism, and excretion (ADME) are the steps of pharmaco/toxicokinetics that determine the internal dose of chemicals to which the organism is exposed. Of all the xenobiotic-metabolizing enzymes, the cytochrome P450 (CYP) enzymes are the most important due to their abundance and versatility. Reactions catalyzed by CYPs usually turn xenobiotics to harmless and excretable metabolites, but sometimes an innocuous xenobiotic is transformed into a toxic metabolite. Data on ADME and toxicity properties of compounds are increasingly generated using in vitro and modeling (in silico) tools.…

Quantitative structure–activity relationshipcytochrome P450In silicoMetabolitexenobioticReviewBiologyPharmacologyXenobiotics03 medical and health scienceschemistry.chemical_compound0302 clinical medicineCYP P450sToxicokineticsPharmacology (medical)aineenvaihdunta030304 developmental biologyADMEPharmacology0303 health sciencesIn silico modelingQSARlcsh:RM1-950Cytochrome P450docking studiesmodelingLigand (biochemistry)3. Good healthbiotransformationslcsh:Therapeutics. PharmacologychemistryBiochemistryin silico030220 oncology & carcinogenesisbiology.proteinXenobioticmetabolismFrontiers in Pharmacology
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Bill2d - a software package for classical two-dimensional Hamiltonian systems

2015

Abstract We present Bill2d , a modern and efficient C++ package for classical simulations of two-dimensional Hamiltonian systems. Bill2d can be used for various billiard and diffusion problems with one or more charged particles with interactions, different external potentials, an external magnetic field, periodic and open boundaries, etc. The software package can also calculate many key quantities in complex systems such as Poincare sections, survival probabilities, and diffusion coefficients. While aiming at a large class of applicable systems, the code also strives for ease-of-use, efficiency, and modularity for the implementation of additional features. The package comes along with a use…

Source codeTheoretical computer scienceComputer sciencechaosmedia_common.quotation_subjectclassical mechanicsFOS: Physical sciencesGeneral Physics and Astronomy01 natural sciences010305 fluids & plasmasHamiltonian systemComputational sciencenumerical simulationsnonlinear dynamicsREADME0103 physical sciences010306 general physicsmedia_commonta114Application programming interfacebusiness.industrydiffusionByteComputational Physics (physics.comp-ph)Modular designmolecular dynamicsIdentifierHardware and ArchitecturetransportbilliardsbusinessPhysics - Computational PhysicsTest data
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