Search results for "binding propertie"

showing 10 items of 15 documents

Utilization of water glass as an activator in the manufacturing of cementitious materials from waste by-products

1987

Abstract In the present paper, the possibility of producing new-type cementless building materials is discussed when water glass as an activating agent is used. The experimental data are presented for a set of raw materials which normally do not show any binding ability. However, if they undergo some physico-chemical treatment and water glass is used, a solid structure of the material is formed. According to the method described here, lots of different mineral waste by-products could be activated, thus gaining binding properties.

Binding abilityMaterials scienceSolid structureWaste managementActivator (phosphor)Binding propertiesGeneral Materials ScienceBuilding and ConstructionCementitiousRaw materialCement and Concrete Research
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Halogen Bonded Analogues of Deep Cavity Cavitands

2014

The first examples of halogen bonded analogues of deep cavity cavitands with guest binding properties, formed between N-alkyl ammonium resorcinarene halides as acceptors and bromotrichloromethane as the donor, are reported in the solid state and in solution.

Binding propertiesMetals and AlloysSolid-stateHalideGeneral ChemistryResorcinarenePhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryResorcinarenes; Cavitands; X-ray Crystallography; Halogen BondsHalogenMaterials ChemistryCeramics and CompositesAmmoniumta116
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Resorcinarene Bis-Thiacrowns: Prospective Host Molecules for Silver Encapsulation

2012

Mixed-donor atom tetramethoxy resorcinarene bis-thiacrown hosts, in which the crown unit contains both hard oxygen and soft sulfur donor atoms, were synthesized for soft metal cation binding. The binding properties were investigated both in solution and in the solid state by NMR spectroscopy and X-ray crystallography. It was found that the resorcinarene bis-thiacrowns were able to complex silver cations with remarkable affinity forming readily 1:2 host–guest complexes in solution. The solid state structures also revealed that the bis-thiacrowns form silver complexes in an unanticipated endo- and exo-cavity fashion within the same host molecule. Both the solution and solid state studies indi…

Cation bindingChemistryStereochemistryOrganic ChemistryBinding propertiesSupramolecular chemistrychemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopyResorcinareneBiochemistrySulfurAtomPolymer chemistryMoleculeta116Chemistry - An Asian Journal
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Forchlorfenuron-mimicking haptens: From immunogen design to antibody characterization by hierarchical clustering analysis

2011

To obtain highly-specific and selective forchlorfenuron binders, a collection of functionalized derivatives with different spacer arm locations and lengths was prepared. By immunization with target-mimicking haptens, a large battery of monoclonal and polyclonal antibodies against this synthetic cell regulator was produced and exhaustively characterized in two immunoassay formats using homologous and heterologous conjugates. Antibodies with IC50 values lower than 0.3 nM were successfully raised from the prepared immunogens, thus evidencing the efficacy of the explored strategies. In order to identify significant epitopes in the antibody-antigen interaction, a series of new chemical forchlorf…

Immunogenantigen binding propertiesForchlorfenuronBiochemistryEpitopeAntibodieschemistry.chemical_compoundStructure-Activity RelationshipBiomimetic MaterialsmedicineStructure–activity relationshipAnimalsCluster AnalysisPhysical and Theoretical ChemistryImmunoassaysimmunogen structureforchlorfenuronbiologymedicine.diagnostic_testMolecular StructureOrganic ChemistryCombinatorial chemistrychemistryPolyclonal antibodiesImmunoassayAntibody Formationbiology.proteinRabbitsAntibodyHaptenHaptens
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Cavitands incorporating a Lewis acid dinickel chelate function as receptors for halide anions.

2015

The halide binding properties of the cavitand [Ni2(L(Me2H4))](2+) (4) are reported. Cavitand 4 exhibits a chelating N3Ni(μ-S)2NiN3 moiety with two square-pyramidal Ni(II)N3S2 units situated in an anion binding pocket of ∼4 Å diameter formed by the organic backbone of the (L(Me2H4))(2-) macrocycle. The receptor reacts with fluoride, chloride (in MeCN/MeOH), and bromide (in MeCN) ions to afford an isostructural series of halogenido-bridged complexes [Ni2(L(Me2H4))(μ-Hal)](+) (Hal = F(-) (5), Cl(-) (6), and Br(-) (7)) featuring a N3Ni(μ-S)2(μ-Hal)NiN3 core structure. No reaction occurs with iodide or other polyatomic anions (ClO4(-), NO3(-), HCO3(-), H2PO4(-), HSO4(-), SO4(2-)). The binding ev…

Inorganic ChemistryStereochemistryChemistryPolymer chemistryBinding propertiesHalideMoietyCavitandChelationLewis acids and basesPhysical and Theoretical ChemistryReceptorInorganic chemistry
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Circular dichroism studies on the interaction of sulfonylureas with insulin

1976

The interaction of 5 sulfonylurea derivatives with insuline was investigated by means of circular dichroism measurements. It was found that all sulfonylureas investigated decrease the ellipticity band of insulin at 208 nm, whereas the band at 222 nm remains unaffected. It is suggested that these observations are due to a change of the insulin conformation, provoked by the interaction of the drugs with insulin. It is assumed that such an effect on the insulin conformation can influence the binding properties of insulin, e.g. in respect to the insulin aggregation, to the binding to insulin antibodies and to a bound, inactive form of insulin in the plasma. Some other drugs have similar, but mo…

PharmacologyCircular dichroismmedicine.medical_specialtyBinding SitesProtein ConformationSwinemedicine.drug_classChemistryCircular DichroismInsulinmedicine.medical_treatmentBinding propertiesPharmacology toxicologyGeneral MedicineInsulin AntibodySulfonylureaSulfonylurea CompoundsEndocrinologyProtein structureInternal medicinemedicineAnimalsInsulinBinding siteNaunyn-Schmiedeberg's Archives of Pharmacology
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“ One Ring to Bind Them All ”—Part I: The Efficiency of the Macrocyclic Scaffold for G-Quadruplex DNA Recognition

2010

International audience; Macrocyclic scaffolds are particularly attractive for designing selective G-quadruplex ligands essentially because, on one hand, they show a poor affinity for the "standard" B-DNA conformation and, on the other hand, they fit nicely with the external G-quartets of quadruplexes. Stimulated by the pioneering studies on the cationic porphyrin TMPyP4 and the natural product telomestatin, follow-up studies have developed, rapidly leading to a large diversity of macrocyclic structures with remarkable-quadruplex binding properties and biological activities. In this review we summarize the current state of the art in detailing the three main categories of quadruplex-binding …

ScaffoldArticle Subjectlcsh:QH426-470Review ArticleBiology010402 general chemistryBioinformaticsRing (chemistry)G-quadruplex01 natural sciencesBiochemistryTelomestatinlcsh:Biochemistrychemistry.chemical_compound[CHIM] Chemical Sciences[CHIM]Chemical Scienceslcsh:QD415-436Molecular BiologyDna recognitionComputingMilieux_MISCELLANEOUSNatural product010405 organic chemistryBinding propertiesPorphyrinCombinatorial chemistry3. Good health0104 chemical scienceslcsh:Geneticschemistry
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The Interaction of Small Molecules with Biomolecules

2014

The binding of small molecules with biological targets is associated to interesting chemical and biological properties of the resulting supramolecular systems. We have recently reported on the synthesis and characterization of cationic first row transition metal complexes and the study of their DNA binding properties, in aqueous solutions at neutral pH, essentially investigated by viscosimetry and spectroscopic techniques such as circular dichroism, absorption and fluorescence in the UV-visible wavelength range. Of course, such procedure cannot furnish atomic level details of the molecule-DNA interaction. Computational Chemistry may provide support for the interpretation of experimental dat…

Settore CHIM/03 - Chimica Generale E Inorganicatransition metal complexes DNA binding properties Molecular Dynamics G-quadruplexSettore CHIM/08 - Chimica Farmaceutica
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Aromatic Bridged Bis-phenol A Derived Cyclophanes. Synthesis, Molecular Structure and Binding Properties Toward Quats

2003

Three novel polyoxyethylene bridged bis phenol A derived cyclophanes, {\rm 2 -- 4,} with additional aromatic units in the bridge to increase the number of cation–π interactions with guest cations, were synthesized and characterized by means of X-ray crystal structure determinations. The binding properties of these receptors toward tetramethylammonium (TMA), N-methylpyridinium (NMP), acetylcholine (ACh) and N-methylquinolinium (NMQ) salts were evaluated by means of 1H NMR spectroscopy and compared with those of the previously reported receptor 1.

Tetramethylammonium1h nmr spectroscopychemistry.chemical_compoundMolecular recognitionchemistryStereochemistryBinding propertiesSupramolecular chemistryPhenolMoleculeGeneral ChemistryCrystal structureMedicinal chemistrySupramolecular Chemistry
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Flavour retention and release from protein solutions

2006

International audience; This paper briefly presents the main results obtained up to now on protein–flavour binding and release in relation with flavour perception. Among the food proteins, β-lactoglobulin is the most extensively studied for its binding properties, which involve both hydrophobic and hydrogen binding. Recent developments using molecular modelling and Quantitative Structure–Activity Relationship confirmed the existence of two different binding sites for flavour compounds on β-lactoglobulin. During the aroma release process in the mouth, not only free aroma compounds are released but also those reversibly bound by the protein, pointing out the fact that flavour perception is on…

[SDV.BIO]Life Sciences [q-bio]/BiotechnologyPROTEINSFlavourBioengineeringLactoglobulins01 natural sciencesApplied Microbiology and Biotechnology0404 agricultural biotechnologyComputational chemistryCyclohexenesHumansBinding siteAromaStrong bindingFlavorBinding SitesbiologyFLAVOUR RELEASETerpenesChemistry010401 analytical chemistryBinding propertiesfood and beveragesSerum Albumin Bovine04 agricultural and veterinary sciencesHydrogen-Ion ConcentrationMilk Proteinsbiology.organism_classification040401 food science0104 chemical sciences[SDV.BIO] Life Sciences [q-bio]/BiotechnologyFlavoring AgentsBiochemistryBenzaldehydesTasteFLAVOUR BINDINGSoybean ProteinsFood TechnologyLimoneneProtein BindingBiotechnology
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