Search results for "binding propertie"

showing 5 items of 15 documents

Binding properties of heptakis-(2,6-di-O-methyl)-β-cyclodextrin and mono-(3,6-anhydro)-β-cyclodextrin: a polarimetric study

2011

The binding constants for the inclusion complexes formed between heptakis-(2,6-di-O-methyl)-β-cyclodextrin (MβCD) and mono-(3,6-anhydro)-β-cyclodextrin (AβCD) with a set of suitably selected organic guests, were measured by means of polarimetry. Measurements were carried out at various pH values in order to ensure the correct protonation state for ionizable guests. Experimental data suggest that the binding properties of MβCD may be rationalized considering the less polar and more hydrophobic character of the cavity, although similar variations in conformational/dynamic behaviour occur as for native βCD. On the other hand, AβCD shows some similarities with αCD, due to the significant distor…

chemistry.chemical_classificationCrystallographyCyclodextrins host-guest complexes polarimetric measurementsCyclodextrinChemistryBinding propertiesSupramolecular chemistryPolarProtonationSettore CHIM/06 - Chimica OrganicaGeneral ChemistryCondensed Matter PhysicsFood ScienceJournal of Inclusion Phenomena and Macrocyclic Chemistry
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Spectrophotometric study on the thermodynamics of binding of α- and β-cyclodextrin towards some p-nitrobenzene derivativesElectronic supplementary in…

2003

Binding properties of native α- and β-cyclodextrin towards some nitrobenzene derivatives have been studied by means of UV-vis spectrophotometry. The former host is able to form complexes having 1 : 1 and 1 : 2 stoichiometric ratios with these guests, while only 1 : 1 complexes are detected with the latter host. A careful analysis of the thermodynamic parameters for complexation equilibria, under the perspective of the enthalpy–entropy compensation effect, reveals that binding abilities of the two different hosts are subject to different features.

chemistry.chemical_classificationP-Nitrobenzenemedicine.diagnostic_testCyclodextrinChemistryStereochemistryOrganic ChemistryBinding propertiesBiochemistryCompensation effectNitrobenzenechemistry.chemical_compoundComputational chemistrySpectrophotometrymedicinePhysical and Theoretical ChemistryStoichiometryOrganic & Biomolecular Chemistry
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Complexation Selectivities of Pillar[5]arenes with Primary Ammonium Salts

2013

The complexation of alkyl-substituted pillar[5]arenes with primary ammonium salts is investigated. 1,4-Bis(methoxy)pillar[5]arene (MeP5) can form strong complexes with the primary ammonium salts in CDCl3. However, 1,4-bis(ethoxy)pillar[5]arene (EtP5) shows weak interaction with these guests, and 1,4-bis(butoxy)pillar[5]arene (BuP5) can not form such a complex at all. These results indicate that the modified alkyl chains of pillar[5]arene play an important role in the complexation selectivity.

chemistry.chemical_classificationPrimary (chemistry)Binding propertiesPillarGeneral ChemistryMedicinal chemistrychemistry.chemical_compoundchemistryAlkoxy groupOrganic chemistryAmmoniumSelectivityHost–guest chemistryAlkylChinese Journal of Chemistry
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Odorant-binding protein-based optoelectronic tongue and nose for sensing volatile organic compounds

2019

International audience; We developed an array of odorant-binding protein mutants with various binding properties. The same design is suitable for the detection and identification of volatile organic compounds (VOCs) both in the liquid phase and in the gas phase by surface plasmon resonance imaging. The obtained optoelectronic tongue is highly selective at low concentrations of VOCs with a low detection limit, but a narrow linear range. In comparison, the optoelectronic nose gives a much higher signal to noise ratio, but the discrimination of VOCs from different chemical classes requires kinetic data to get rid of non-specific signals. This work shows that these optoelectronic tongue and nos…

electronic nosevolatile organic compoundMaterials scienceElectronic tongueodorant-binding proteins02 engineering and technologyelectronic tongue01 natural sciences[CHIM.ANAL]Chemical Sciences/Analytical chemistrySurface plasmon resonance imaging[CHIM]Chemical SciencesVolatile organic compoundComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationDetection limitElectronic nosebiologybusiness.industry[CHIM.ORGA]Chemical Sciences/Organic chemistry010401 analytical chemistryBinding properties[CHIM.ORGA] Chemical Sciences/Organic chemistry021001 nanoscience & nanotechnology0104 chemical sciences[SDV.AEN] Life Sciences [q-bio]/Food and NutritionchemistryLinear rangeOdorant-binding proteinbiology.proteinOptoelectronicssurface plasmon resonance imaging0210 nano-technologybusiness[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
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Binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assays.

2017

Three polyaminocyclodextrin materials, obtained by direct reaction between heptakis(6-deoxy-6-iodo)-β-cyclodextrin and the proper linear polyamines, were investigated for their binding properties, in order to assess their potential applications in biological systems, such as vectors for simultaneous drug and gene cellular uptake or alternatively for the protection of macromolecules. In particular, we exploited polarimetry to test their interaction with some model p-nitroaniline derivatives, chosen as probe guests. The data obtained indicate that binding inside the host cavity is mainly affected by interplay between Coulomb interactions and conformational restraints. Moreover, simultaneous i…

nitroanilineaminocyclodextrins; binding properties; nitroanilines; pDNA; polarimetry; supramolecular chemistrySupramolecular chemistryaminocyclodextrins010402 general chemistry01 natural sciencesFull Research Papersupramolecular chemistryaminocyclodextrinlcsh:QD241-441lcsh:Organic chemistrypDNABioassaybinding propertielcsh:Sciencepolarimetry010405 organic chemistryChemistryBinding propertiesOrganic ChemistryCationic polymerizationnitroanilines0104 chemical sciencesChemistrybinding propertiesPolynucleotideBiophysicslcsh:QpUC19Direct reactionMacromoleculeBeilstein journal of organic chemistry
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