Search results for "Moi"

showing 10 items of 2109 documents

Spectroscopic studies of the interaction of 3-(2-thienyl)-[1,2,3]triazolo[1,5-a]pyridine with 2,6-dimethyl-β-cyclodextrin and ctDNA

2016

The inclusion complexation behavior of 3-(2-thienyl)-[1,2,3]triazolo[1,5-a] pyridine (TTP) with native β-cyclodextrin and derivatized cyclodextrins was investigated. Stability constants for complexes with 1 : 1 molar ratios were calculated from phase solubility diagrams. The solubilizing efficiency of the TTP inclusion complex is enhanced in the order of DMβCD > HPβCD > βCD. The TTP-DMβCD inclusion complex was further characterized in solution by means of absorption, fluorescence, 2D NMR and molecular modeling methods. The thermodynamic studies indicate that the inclusion of TTP into the cyclodextrin cavity is mainly an enthalpy-driven process. The 2D NMR studies revealed that the thienyl m…

Models MolecularPyridinesStereochemistryIntercalation (chemistry)Antineoplastic Agents010402 general chemistry01 natural sciencesBiochemistryHydrophobic effectchemistry.chemical_compoundPyridineCarbohydrate ConformationAnimalsMoietyPhysical and Theoretical ChemistrySolubilitychemistry.chemical_classificationCyclodextrin010405 organic chemistrySpectrum Analysisbeta-CyclodextrinsOrganic ChemistryDNATriazoles0104 chemical sciencesCrystallographychemistryDocking (molecular)CattleTwo-dimensional nuclear magnetic resonance spectroscopyOrganic & Biomolecular Chemistry
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Structures of yeast peroxisomal Δ(3),Δ(2)-enoyl-CoA isomerase complexed with acyl-CoA substrate analogues: the importance of hydrogen-bond networks f…

2015

Δ3,Δ2-Enoyl-CoA isomerases (ECIs) catalyze the shift of a double bond from 3Z- or 3E-enoyl-CoA to 2E-enoyl-CoA. ECIs are members of the crotonase superfamily. The crotonase framework is used by many enzymes to catalyze a wide range of reactions on acyl-CoA thioesters. The thioester O atom is bound in a conserved oxyanion hole. Here, the mode of binding of acyl-CoA substrate analogues to peroxisomalSaccharomyces cerevisiaeECI (ScECI2) is described. The best defined part of the bound acyl-CoA molecules is the 3′,5′-diphosphate-adenosine moiety, which interacts with residues of loop 1 and loop 2, whereas the pantetheine part is the least well defined. The catalytic base, Glu158, is hydrogen-bo…

Models MolecularSaccharomyces cerevisiae ProteinsDouble bondStereochemistryProtein ConformationIsomeraseSaccharomyces cerevisiaeEnoyl CoA isomeraseThioesterPhotochemistryDodecenoyl-CoA Isomerasebeta-oxidationSubstrate SpecificityStructural Biologyddc:570Catalytic DomainEnzyme StabilitySide chainMoietyta116chemistry.chemical_classificationHydrogen bondenoyl-CoA isomeraseta1182Hydrogen BondingGeneral Medicinehydrogen-bond networkcrotonaseoxyanion holechemistryAcyl Coenzyme AOxyanion holeOxidation-ReductionProtein BindingActa crystallographica. Section D, Biological crystallography
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A new approach to inhibit human β-tryptase by protein surface binding of four-armed peptide ligands with two different sets of arms

2013

A series of six new tetravalent ligands (1-6) with two different sets of arms bind to the surface of β-tryptase, a tetrameric enzyme with an A(2)B(2) arrangement of its four monomers and two different binding sites on its protein surface (as suggested by a docking study). Besides proteinogenic amino acids also the guanidiniocarbonyl pyrrole cation (abbreviated as GCP), as an artificial arginine analog, was introduced into the arms of the ligands to investigate its influence on protein surface binding and enzyme inhibition. Furthermore, four ligands (7-10) with four identical arms also containing the GCP group were additionally synthesized to study the influence of the GCP moiety on the inhi…

Models MolecularSerine Proteinase InhibitorsArginineStereochemistrySurface PropertiesChemieLigandsBiochemistryGuanidineschemistry.chemical_compoundStructure-Activity RelationshipMoietyHumansPyrrolesAmino Acid SequencePhysical and Theoretical ChemistryBinding sitechemistry.chemical_classificationBinding SitesMolecular StructureOrganic ChemistryLigand (biochemistry)Combinatorial chemistryAmino acidEnzymeMonomerchemistryDocking (molecular)TryptasesPeptidesBiologie
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Synthesis of a potent photoreactive acidic γ-secretase modulator for target identification in cells.

2012

Supramolecular self-assembly of amyloidogenic peptides is closely associated with numerous pathological conditions. For instance, Alzheimer´s disease (AD) is characterized by abundant amyloid plaques originating from the proteolytic cleavage of the amyloid precursor protein (APP) by β- and γ-secretases. Compounds named γ-secretase modulators (GSMs) can shift the substrate cleavage specificity of γ-secretase toward the production of non-amyloidogenic, shorter Aβ fragments. Herein, we describe the synthesis of highly potent acidic GSMs, equipped with a photoreactive diazirine moiety for photoaffinity labeling. The probes labeled the N-terminal fragment of presenilin (the catalytic subunit of …

Models MolecularStereochemistryProtein subunitClinical BiochemistrySupramolecular chemistryPharmaceutical ScienceCHO CellsCleavage (embryo)BiochemistryPresenilinStructure-Activity Relationshipchemistry.chemical_compoundCricetinaeDrug DiscoveryAmyloid precursor proteinAnimalsMoietyMolecular BiologyDose-Response Relationship DrugMolecular StructurePhotoaffinity labelingbiologyAzirinesChemistryOrganic ChemistryPhotochemical ProcessesBiochemistryDiazirinebiology.proteinMolecular MedicineAmyloid Precursor Protein Secretases
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Pentamethylcyclopentadienyl-rhodium and iridium complexes containing (N^N and N^O) bound chloroquine analogue ligands: synthesis, characterization an…

2016

The synthesis and characterization of twenty new pentamethylcyclopentadienyl-rhodium and iridium complexes containing N^N and N^O-chelating chloroquine analogue ligands are described. The in vitro antimalarial activity of the new ligands as well as the complexes was evaluated against the chloroquine sensitive (CQS) NF54 and the chloroquine resistant (CQR) Dd2 strains of Plasmodium falciparum. The antimalarial activity was found to be good to moderate; although all complexes are less active than artesunate, some of the ligands and complexes showed better activity than chloroquine (CQ). In particular, rhodium complexes were found to be considerably more active than iridium complexes against t…

Models Molecularantimalarial propertiesStereochemistryPlasmodium falciparumDrug ResistanceMolecular Conformationchemistry.chemical_elementCrystal structureChemistry Techniques Synthetic010402 general chemistryIridiumLigands01 natural sciencesChlorideRhodiumIridium and Rhodium complexes chloroquine analog ligands Crystal structures in vitro antimalarian activityInorganic Chemistrychemistry.chemical_compoundAntimalarialsmedicineOrganometallic CompoundsMoietyRhodiumIridiumta116iridium complexesGroup 2 organometallic chemistrySchiff basechloroquine analogue ligands010405 organic chemistrypentamethylcyclopentadienyl-rhodium complexesChloroquine0104 chemical scienceschemistryDerivative (chemistry)medicine.drug
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Structural and Molecular Characterization of meso-Substituted Zinc Porphyrins: A DFT Supported Study

2011

Structural parameters of a range of over 100 meso-substituted zinc porphyrins were reviewed and compared to show how far the nature of the functional group may affect the interatomic distances and bond angles within the porphyrin core. It was proved that even despite evident deformations of the molecular structure, involving twisting of the porphyrin's central plane, the coupled π-bonding system remains flexible and stable. DFT calculations were applied to a number of selected porphyrins representative for the reviewed compounds to emphasize the relevance of theoretical methods in structural investigations of complex macrocyclic molecular systems. Experimental and DFT-simulated IR spectral …

Models Molecularzinc porphyrins; molecular structure; DFT theoretical calculations; IR spectraPorphyrinsSpectrophotometry InfraredStereochemistrySurface PropertiesPharmaceutical Sciencechemistry.chemical_elementInfrared spectroscopyContext (language use)molecular structureZincCrystallography X-RayVibrationArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundDFT theoretical calculationslcsh:Organic chemistryComputational chemistryDrug Discoveryzinc porphyrins molecular structure DFT theoretical calculations IR spectraSpectroscopy Fourier Transform InfraredMoleculeMoietyComputer SimulationPyrrolesPhysical and Theoretical ChemistryIR spectraOrganic ChemistryPorphyrinzinc porphyrinsZincMolecular geometrychemistryModels ChemicalChemistry (miscellaneous)Functional groupMicroscopy Electron ScanningMolecular MedicineQuantum TheoryMolecules
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Protecting Groups

1991

There is hardly any area of preparative organic chemistry in which the proper use of protecting groups is not a prerequisite for the successful achievement of the goals aimed at. For this reason such blocking functions have been developed for nearly 100 years by numerous researchers from all disciplines of organic chemistry, and consequently solutions to the existing problems have been devised, making use of various synthetic transformations. It was Fischer who, among his many important contributions to chemistry, first realized that the application of protecting functions is often a necessity for a successful synthesis. Thus, he introduced the isopropylidene ketal in carbohydrate chemistry…

MoietyBiochemical engineering
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Seikkailija Paul Moij : Viipurin valta- ja vastakulttuurit 1600-luvun jälkipuoliskolla

2017

Moij PaulvastakulttuuritViipurihistoriakulttuurihistoriavaltarakenteet1600-luku
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Vita Moysis / [Laurentius Aretinus

1485

Sense sign. - Sense data L. gòt. - 32-34 lín. - Min. p. inic. - Filigr.: flor de lis. - Sense fol.

Moisès (Líder bíblic) Obres anteriors a 1800DIG-BH
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Effect of moisture on elastic and viscoelastic properties of fiber reinforced plastics: Retrospective and current trends

2019

Abstract This chapter is a brief review of journal papers and books about moisture and composites with polymer matrix (mostly fiber reinforced composites but not exclusively). Most polymer materials and composites absorb moisture. It is well known from many papers (some of them mentioned in this chapter) over several decades that absorbed moisture essentially affects mechanical and many other important properties of polymers and polymer-based composites. The key question is: How does absorbed moisture affect mechanical properties of composites? Furthermore, the process of moisture absorption in composite structures may occur over many months and even years. More questions then arise: What i…

Moisture absorptionMaterials scienceMoisturePolymer scienceComposite numberNew materialsFiberFiber-reinforced compositeCurrent (fluid)Viscoelasticity
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