Search results for "Models"

showing 10 items of 8211 documents

Tyrosinase Enzyme: 1. An Overview on a Pharmacological Target

2014

The tyrosinase enzyme (EC 1.14.18.1) is an oxidoreductase inside the general enzyme classification and is involved in the oxidation and reduction process in the epidermis. These chemical reactions that the enzyme catalyzes are of principal importance in the melanogenesis process. This process of melanogenesis is related to the melanin formation, a heteropolymer of indolic nature that provides the different tonalities in the skin and helps to the protection from the ultraviolet radiation. However, a pigment overproduction, come up by the action of the tyrosinase, can cause different disorders in the skin related to the hyperpigmentation. Several studies mainly focused on the characteristics …

Models Molecularchemistry.chemical_classificationMolecular StructureEpidermis (botany)Monophenol MonooxygenaseTyrosinaseGeneral MedicineHyperpigmentationMelaninStructure-Activity RelationshipEnzymechemistryBiochemistryOxidoreductaseDrug DiscoveryMolecular mechanismmedicineAnimalsHumansEnzyme Inhibitorsmedicine.symptomOverproductionCurrent Topics in Medicinal Chemistry
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Novel Hexanuclear Copper(II) Complex Built from a Simple Tetrachelating Triazole Ligand: Synthesis, Structure, and Magnetism

2013

A new easy symmetric 3,5-disubstituted 1,2,4-triazole ligand (H3diV) by reaction with an excess of copper(II) salt has afforded a novel hexanuclear compound (Cu/HdiV ratio of 6:2) through a bis(trans-cis-cis-trans) binding mode, exhibiting two types of Cu(II) centers and two clearly distinguishable antiferromagnetic J1 (-234 cm(-1)) and J2 (-35 cm(-1)) coupling constants.

Models Molecularchemistry.chemical_classificationMolecular StructureStereochemistryLigandMagnetismMagnetic PhenomenaTemperatureTriazoleSalt (chemistry)chemistry.chemical_elementTriazolesLigandsCopperInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryOrganometallic CompoundsPhysical and Theoretical ChemistryCopperInorganic Chemistry
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N-[tert-Butoxycarbonylglycyl-(Z)-α,β-dehydrophenylalanylglycyl-(E)-α,β-dehydrophenylalanylphenylalanyl]-4-nitroaniline ethanol solvate

2005

The alpha,beta-dehydrophenylalanine residues influence the conformation of the title pentapeptide Boc0-Gly1-Delta(Z)Phe2-Gly3-Delta(E)Phe4-L-Phe5-p-NA ethanol solvate, C42H43N7O9.C2H5OH. The first unsaturated phenylalanyl (Delta(Z)Phe2) and the third glycyl (Gly3) residues form a type I beta turn, while the second unsaturated phenylalanyl (Delta(E)Phe4) and the last phenylalanyl (L-Phe5) residues are part of a type II beta turn. All the amino acids in the peptide are linked trans to one another. The crystal structure is stabilized by intra- and intermolecular hydrogen bonds.

Models Molecularchemistry.chemical_classificationOligopeptideAniline CompoundsEthanolMolecular StructureHydrogen bondStereochemistryPeptideGeneral MedicineCrystal structureCrystallography X-RayPentapeptide repeatGeneral Biochemistry Genetics and Molecular BiologyAmino acidchemistry.chemical_compoundchemistryMoleculeOligopeptidesActa Crystallographica Section C Crystal Structure Communications
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Self-assembly of semiflexible polymers confined to thin spherical shells

2018

Confinement effects are critical for stiff macromolecules in biological cells, vesicles, and other systems in soft matter. For these molecules, the competition between the packing entropy and the enthalpic cost of bending is further shaped by strong confinement effects. Through coarse-grained molecular dynamics simulations, we explore the self-assembly of semiflexible polymers confined in thin spherical shells for various chain lengths, chain stiffnesses, and shell thicknesses. Here, we focus on the case where the contour and persistence length of the polymers are comparable to the radius of the confining cavity. The range of ordered structures is analyzed using several order parameters to …

Models Molecularchemistry.chemical_classificationPersistence lengthMaterials scienceCondensed matter physicsPolymersMolecular Conformation02 engineering and technologyGeneral ChemistryPolymer021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesSpherical shellTopological defectCondensed Matter::Soft Condensed MatterMolecular dynamicschemistryLiquid crystal0103 physical sciencesMonolayerSoft matter010306 general physics0210 nano-technologyMechanical PhenomenaSoft Matter
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Coordination Chemistry of 6-Thioguanine Derivatives with Cobalt: Toward Formation of Electrical Conductive One-Dimensional Coordination Polymers

2013

In this work we have synthetized and characterized by X-ray diffraction five cobalt complexes with 6-thioguanine (6-ThioGH), 6-thioguanosine (6-ThioGuoH), or 2'-deoxy-6-thioguanosine (2'-d-6-ThioGuoH) ligands. In all cases, these ligands coordinate to cobalt via N7 and S6 forming a chelate ring. However, independently of reagents ratio, 6-ThioGH provided monodimensional cobalt(II) coordination polymers, in which the 6-ThioG(-) acts as bridging ligand. However, for 2'-d-6-ThioGuoH and 6-ThioGuoH, the structure directing effect of the sugar residue gives rise to mononuclear cobalt complexes which form extensive H-bond interactions to generate 3D supramolecular networks. Furthermore, with 2'-d…

Models Molecularchemistry.chemical_classificationPolymersElectric ConductivitySupramolecular chemistrychemistry.chemical_elementBridging ligandCobaltPolymerCoordination complexInorganic ChemistryMolecular wireX-Ray DiffractionchemistryCoordination ComplexesPolymer chemistryX-ray crystallographyChelationPhysical and Theoretical ChemistryThioguanineCobaltInorganic Chemistry
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Theoretical Study of the Hydroxyl Radical Addition to Uracil and Photochemistry of the Formed U6OH• Adduct

2014

Hydroxyl radical ((•)OH) is produced in biological systems by external or endogenous agents. It can damage DNA/RNA by attacking pyrimidine nucleobases through the addition to the C5═C6 double bond. The adduct resulting from the attachment at the C5 position prevails in the experimental measurements, although the reasons for this preference remain unclear. The first aim of this work is therefore to shed light on the comprehension of this important process. Thus, the thermal (•)OH addition to the C5═C6 double bond of uracil has been studied theoretically by using DFT, MP2, and the multiconfigurational CASPT2//CASSCF methodologies. The in-vacuo results obtained with the latter protocol plus th…

Models Molecularchemistry.chemical_classificationPyrimidineDouble bondHydroxyl RadicalPhotochemistryUracilPhotochemistrySurfaces Coatings and FilmsAdductNucleobaseDNA Adductschemistry.chemical_compoundchemistryMaterials ChemistryQuantum TheoryHydroxyl radicalPhysical and Theoretical ChemistrySolvent effectsUracilVisible spectrumThe Journal of Physical Chemistry B
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Density functional theory fragment descriptors to quantify the reactivity of a molecular family: Application to amino acids

2007

By using the exact density functional theory, one demonstrates that the value of the local electronic softness of a molecular fragment is directly related to the polarization charge (Coulomb hole) induced by a test electron removed (or added) from (at) the fragment. Our finding generalizes to a chemical group a formal relation between these molecular descriptors recently obtained for an atom in a molecule using an approximate atomistic model [P. Senet and M. Yang, J. Chem. Sci. 117, 411 (2005)]. In addition, a practical ab initio computational scheme of the Coulomb hole and related local descriptors of reactivity of a molecular family having in common a similar fragment is presented. As a b…

Models Molecularchemistry.chemical_classificationQuantitative Biology::BiomoleculesQuantitative structure–activity relationshipBinding SitesChemistryAb initioGeneral Physics and AstronomyAmino acidModels ChemicalAb initio quantum chemistry methodsComputational chemistryMolecular descriptorMoleculeComputer SimulationDensity functional theoryAmino AcidsPhysical and Theoretical ChemistryAlgorithmsFragment molecular orbitalProtein BindingThe Journal of Chemical Physics
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Collective properties of hydration: long range and specificity of hydrophobic interactions

1997

We report results of molecular dynamics (MD) simulations of composite model solutes in explicit molecular water solvent, eliciting novel aspects of the recently demonstrated, strong many-body character of hydration. Our solutes consist of identical apolar (hydrophobic) elements in fixed configurations. Results show that the many-body character of PMF is sufficiently strong to cause 1) a remarkable extension of the range of hydrophobic interactions between pairs of solute elements, up to distances large enough to rule out pairwise interactions of any type, and 2) a SIF that drives one of the hydrophobic solute elements toward the solvent rather than away from it. These findings complement re…

Models Molecularchemistry.chemical_classificationRange (particle radiation)BiomoleculeBiophysicsWaterEnergy landscapeSolutionsFolding (chemistry)Hydrophobic effectMolecular dynamicsCharacter (mathematics)Models ChemicalchemistryChemical physicsComputational chemistrySolventsProtein recognitionThermodynamicsComputer SimulationResearch ArticleBiophysical Journal
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Mass spectrometric studies on small open-chain piperazine-containing ligands and their transition metal complexes

2001

Electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry was used to characterize the complexes formed between open-chain piperazine-containing ligands and transition metal salts (Cobalt, Copper, Zinc, and Cadmium as chlorides, nitrates, and acetates). Only single-charged complexes were observed, formed of one ligand (L) and mainly one metal ion (M). Since the net charge of the complexes was one, a counterion (X) was attached to some of the complexes, with formation of [L + M + X]+ complexes, and a proton was lost from others, as in [L − H + M]+ complexes. In most cases the composition of the complexes was more dependent on the ligand than the metal salt. Collisio…

Models Molecularchemistry.chemical_classificationSpectrometry Mass Electrospray IonizationFourier AnalysisLigandMetal ions in aqueous solutionInorganic chemistryMolecular ConformationCobaltLigandsPiperazinesFourier transform ion cyclotron resonanceNon-innocent ligandStructure-Activity RelationshipZincchemistry.chemical_compoundCrystallographychemistryTransition metalMetalsCarboxylateCounterionMetal aquo complexCopperSpectroscopyJournal of Mass Spectrometry
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Chelate Cooperativity and Spacer Length Effects on the Assembly Thermodynamics and Kinetics of Divalent Pseudorotaxanes

2011

Homo- and heterodivalent crown-ammonium pseudorotaxanes with different spacers connecting the two axle ammonium binding sites have been synthesized and characterized by NMR spectroscopy and ESI mass spectrometry. The homodivalent pseudorotaxanes are investigated with respect to the thermodynamics of divalent binding and to chelate cooperativity. The shortest spacer exhibits a chelate cooperativity much stronger than that of the longer spacers. On the basis of crystal structure, this can be explained by a noninnocent spacer, which contributes to the binding strength in addition to the two binding sites. Already very subtle changes in the spacer length, i.e., the introduction of an additional…

Models Molecularchemistry.chemical_classificationSpectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyRotaxanesCooperative bindingThermodynamicsCooperativityGeneral ChemistryCrystal structureNuclear magnetic resonance spectroscopyBiochemistryCatalysisDivalentQuaternary Ammonium CompoundsKineticschemistry.chemical_compoundColloid and Surface ChemistrychemistryIntramolecular forceEffective molarityThermodynamicsMethyleneta116Chelating AgentsJournal of the American Chemical Society
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