Search results for "Molecular mechanics"

showing 10 items of 55 documents

Modeling ?-lactam interactions in aqueous solution through combined quantum mechanics-molecular mechanics methods

1999

Computational MathematicsMolecular dynamicschemistry.chemical_compoundAqueous solutionChemistryComputational chemistryβ lactamsLactamDensity functional theoryGeneral ChemistrySolvent effectsMolecular mechanicsJournal of Computational Chemistry
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Reliability of Virtual Screening Methods in Prediction of PDE4Binhibitor Activity

2015

Identification of active ligands using computational methods is a challenging task. For example, molecular docking, pharmacophore modeling, and three dimensional quantitative structure-activity relationship models (3D-QSAR) are widely used methods to identify novel small molecules. However, all these methods have, in addition to advantages, also significant pitfalls. The aim of this study was to compare some commonly used computational methods to estimate their ability to separate highly active PDE4B-inhibitors from less active and inactive ones. Here, 152 molecules with pIC 50 -range of 3.4-10.5, originating from six original studies were used. High correlation coefficients by using dockin…

Computer scienceQuantitative Structure-Activity RelationshipMultiple methodsLigandsComputers MolecularDrug DiscoveryProtein Interaction MappingHumansSimulationPharmacological Phenomenathree-dimensional quantitative structure-activity relationshipVirtual screeningbusiness.industryta1182Pattern recognitionmolecular dockingmolecular mechanics-generalized born-surface areavirtual screeningCyclic Nucleotide Phosphodiesterases Type 4Molecular Docking SimulationDocking (molecular)pharmacophore modelingArtificial intelligencePhosphodiesterase 4 InhibitorsPharmacophorebusinessphosphodiesteraseCurrent Drug Discovery Technologies
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Structural Studies on Polyaza[n]paracyclophanes. A Molecular Mechanics and Crystallographic Study

1997

Abstract Structural analysis of polyaza[n]paracyclophanes 1-5 has been carried out by the use of molecular mechanics and other techniques. NMR data and molecular mechanics calculations show that conformations in which the polyamine chain is arching above the aromatic ring are prevalent in solution. The crystal structure of triprotonated durene derivative 2b agrees with those studies. Crystals of 3H+.2b are triclinic, space group P1, with a = 11.758(4) A, b = 13.870(5) A, c = 17.181(3) A, α = 96.66(2)°, β = 106.02(2)°, γ = 104.87(3)°, Z = 4, R1 = 0.072, wR2 = 0.18. Three different conformations are present in the crystal. Good agreement between the crystal structures and calculated conformat…

CrystalSolventchemistry.chemical_compoundCrystallographyChemistryDureneGeneral ChemistryCrystal structureTriclinic crystal systemRing (chemistry)Molecular mechanicsDerivative (chemistry)Supramolecular Chemistry
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On the interaction of doxorubicin with polynucleotides

2014

The interaction of doxorubicin (DX) with model polynucleotides poly(dG-dC)·poly(dG-dC) (polyGC), poly(dA-dT)·poly(dA-dT) (poly-AT), and calf thymus DNA has been studied by several spectroscopic techniques in phosphate buffer aqueous solutions. UV−vis, circular dichroism, and fluorescence spectroscopic data confirm that intercalation is the prevailing mode of interaction, and also reveal that the interaction with AT-rich regions leads to the transfer of excitation energy to DX not previously documented in the literature. Moreover, the DX affinity for AT sites has been found to be on the same order of magnitude as that reported for GC sites.

DoxorubicinPolynucleotideSettore CHIM/03 - Chimica Generale E Inorganicamolecular mechanics calculationsfluorescencecircular dichroism
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Molecular dynamics simulations of elementary chemical processes in liquid water using combined density functional and molecular mechanics potentials.…

1997

The first molecular dynamics (MD) simulation of a chemical process in solution with an ab initio description of the reactant species and a classical representation of the solvent is presented. We study the dynamics of proton (deuterium) transfer in strongly hydrogen-bonded systems characterized by an energy surface presenting a double well separated by a low activation barrier. We have chosen the hydroxyl-water complex in liquid water to analyze the coupling between the reactive system and the environment. The proton is transferred from one well to the other with a frequency close to 1 ps−1 which is comparable to the low-frequency band associated to hindered translations, diffusional transl…

Hydrogen bonds ; Molecular dynamics method ; Ab initio calculations Ion exchange ; Solvent effects ; Reaction kinetics theory ; Density functional theory ; Intermolecular mechanicsProtonChemistryGeneral Physics and AstronomyIntermolecular mechanicsMolecular dynamics methodHydrogen bondsUNESCO::FÍSICA::Química físicaMolecular dynamicsAb initio calculations Ion exchangeDeuteriumReaction dynamicsChemical physicsComputational chemistryAb initio quantum chemistry methodsSolvent effectsReaction kinetics theoryDensity functional theoryDensity functional theoryPhysical and Theoretical ChemistrySolvent effectsChemical equilibrium:FÍSICA::Química física [UNESCO]
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Scalable Constant pH Molecular Dynamics in GROMACS

2022

Molecular dynamics (MD) computer simulations are used routinely to compute atomistic trajectories of complex systems. Systems are simulated in various ensembles, depending on the experimental conditions one aims to mimic. While constant energy, temperature, volume, and pressure are rather straightforward to model, pH, which is an equally important parameter in experiments, is more difficult to account for in simulations. Although a constant pH algorithm based on the λ-dynamics approach by Brooks and co-workers [Kong, X.; Brooks III, C. L. J. Chem. Phys.1996, 105, 2414–2423] was implemented in a fork of the GROMACS molecular dynamics program, uptake has been rather limited, presumably due to…

ImidazolesmolekyylitpotentiaalienergiaHydrogen-Ion ConcentrationMolecular Dynamics Simulationmonomerspeptides and proteinsreaktiomekanismitmolecular mechanicspotential energyComputer Science Applicationsreaction mechanismspeptiditHumansmolekyylidynamiikkaproteiinitPhysical and Theoretical ChemistryAlgorithms
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Construction of Spirooxindole Analogues Engrafted with Indole and Pyrazole Scaffolds as Acetylcholinesterase Inhibitors

2021

Twenty-five new hits of spirooxindole analogs 8a–y engrafted with indole and pyrazole scaffolds were designed and constructed via a [3+2]cycloaddition (32CA) reaction starting from three components: new chalcone-based indole and pyrazole scaffolds 5a–d, substituted isatins 6a–c, and secondary amines 7a–d. The potency of the compounds were assessed in modulating cholinesterase (AChE) activity using Ellman’s method. Compounds 8i and 8y showed the strongest acetylcholine esterase inhibition (AChEI) with IC50 values of 24.1 and 27.8 μM, respectively. Molecular docking was used to study their interaction with the active site of hAChE. peerReviewed

Indole testChemistryStereochemistrybioaktiiviset yhdisteetGeneral Chemical EngineeringGeneral ChemistryPyrazoleindolespeptides and proteinsAcetylcholinesterasemolecular mechanicsArticleinhibitionchemistry.chemical_compoundChemistryscaffoldsQD1-999orgaaniset yhdisteetinhibiittorit
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Hydrogen abstraction by photoexcited benzophenone: consequences for DNA photosensitization

2016

International audience; We report a computational investigation of the hydrogen abstraction (H-abstraction) induced by triplet benzophenone (3BP) on thymine nucleobase and backbone sugar. The chemical process is studied using both high level multiconfigurational perturbation and density functional theory. Both methods show good agreement in predicting small kinetic barriers. Furthermore the behavior of benzophenone in DNA is simulated using molecular dynamics and hybrid quantum mechanics/molecular mechanics methods. The accessibility of benzophenone to the labile hydrogens within B-DNA is demonstrated, as well as the driving force for this reaction. We evidence a strong dependence of the H-…

LightHydrogenGeneral Physics and Astronomychemistry.chemical_element02 engineering and technologyMolecular Dynamics Simulation010402 general chemistryPhotochemistryHydrogen atom abstraction01 natural sciencesMolecular mechanicsNucleobaseBenzophenoneschemistry.chemical_compoundMolecular dynamicsComputational chemistryBenzophenoneComputer Simulation[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyPhysical and Theoretical ChemistryDNA021001 nanoscience & nanotechnology[INFO.INFO-MO]Computer Science [cs]/Modeling and Simulation0104 chemical sciencesThyminechemistryDensity functional theory0210 nano-technologyHydrogen
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Circular Dichroism of DNA G-Quadruplexes: Combining Modeling and Spectroscopy To Unravel Complex Structures

2016

We report on the comparison between the computational and experimental determination of electronic circular dichroism spectra of different guanine quadruplexes obtained from human telomeric sequences. In particular the difference between parallel, antiparallel, and hybrid structures is evidenced, as well as the induction of transitions between the polymorphs depending on the solution environment. Extensive molecular dynamics simulations (MD) are used to probe the conformational space of the different quadruplexes, and subsequently state-of-the-art hybrid quantum mechanics/molecular mechanics (QM/MM) techniques coupled with excitonic semiempirical Hamiltonian are used to simulate the macromo…

Materials Chemistry2506 Metals and Alloys0301 basic medicineCircular dichroismSurfaces Coatings and FilmNanotechnologyMolecular Dynamics Simulation010402 general chemistryG-quadruplexAntiparallel (biochemistry)01 natural sciencesMolecular mechanics03 medical and health sciencesMolecular dynamicschemistry.chemical_compoundG-QuadruplexeMaterials ChemistryHumans[CHIM]Chemical SciencesPhysical and Theoretical ChemistrySpectroscopyComputingMilieux_MISCELLANEOUSPhysicsQuantitative Biology::BiomoleculesCircular DichroismDNA0104 chemical sciencesSurfaces Coatings and FilmsG-Quadruplexes030104 developmental biologychemistrySettore CHIM/03 - Chimica Generale E InorganicaChemical physicsNucleic Acid ConformationQuantum TheoryDNAHumanMacromoleculeThe Journal of Physical Chemistry B
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Selective targeting of PARP-1 zinc finger recognition domains with Au(III) organometallics

2018

The binding of Au(iii) complexes to the zinc finger domain of the anticancer drug target PARP-1 was studied using a hyphenated mass spectrometry approach combined with quantum mechanics/molecular mechanics (QM/MM) studies. Competition experiments were carried out, whereby each Au complex was exposed to two types of zinc fingers. Notably, the cyclometallated Au-C^N complex was identified as the most selective candidate to disrupt the PARP-1 zinc finger domain, forming distinct adducts compared to the coordination compound Auphen.

Materials Chemistry2506 Metals and AlloysStereochemistryPoly ADP ribose polymeraseSurfaces Coatings and FilmCeramics and Composite010402 general chemistryMass spectrometry01 natural sciencesMolecular mechanicsCatalysisCoordination complexAdductCatalysiMaterials Chemistrychemistry.chemical_classificationZinc finger010405 organic chemistryElectronic Optical and Magnetic MaterialChemistry (all)Metals and AlloysGeneral ChemistryAnticancer drug0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistrySettore CHIM/03 - Chimica Generale E InorganicaCeramics and Composites2506
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