Search results for "molecular recognition"

showing 10 items of 112 documents

ChemInform Abstract: Self-Assembly of Amphiphilic Calixarenes and Resorcinarenes in Water

2011

The calixarenes and resorcinarenes are macrocyclic phenolic molecules that can be modified “a facon” and a wide range of chemical modification strategies have been published over the last 30 years. Because of their remarkable structural properties and their relative ease of chemical modification, they represent excellent and highly versatile bases to design complex building blocks capable of self-assembly and molecular recognition. They have been widely studied for their ability to form supramolecular structures targeting a wide range of applications. The possibility to regio(rim)-selectively modify these macrocycles with different polar and apolar moieties provides synthetic chemists with …

Molecular recognitionChemistryAmphiphileCalixareneSupramolecular chemistryChemical modificationMoleculeNanotechnologyGeneral MedicineSelf-assemblyChemInform
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Cover Picture: A Biocatalytic Nanomaterial for the Label-Free Detection of Virus-Like Particles (ChemBioChem 11/2017)

2017

Molecular recognitionChemistryOrganic ChemistryMolecular MedicineNanoparticleCover (algebra)NanotechnologyMolecular BiologyBiochemistryNanomaterialsLabel freeChemBioChem
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ChemInform Abstract: Dimeric Resorcin[4]arene Capsules in the Solid State

2012

Supramolecular chemistry research is focused on the study of weak non-covalent intermolecular — that is, supramolecular — interactions as the driving force in self-assembly and molecular recognition. Dimeric resorcin[4]arenes capsules have been a focus of our research for the last 15 years. This review describes the solid state complexation studies of unsubstituted phenolic resorcin[4]arenes and pyrogall[4]arenes towards the formation of dimeric capsules and assemblies using ionic and neutral species as guest molecules and templates. The multitude of different crystal structures obtained during these studies demonstrates the versatile nature of resorcin[4]arenes and pyrogall[4]arenes (2-hyd…

Molecular recognitionChemistryPolymer chemistryIntermolecular forceSolid-stateSupramolecular chemistryMoleculeIonic bondingGeneral MedicineCrystal structureCrystal engineeringChemInform
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Dimeric Resorcin[4jarene Capsules in the Solid State

2011

Supramolecular chemistry research is focused on the study of weak non-covalent intermolecular — that is, supramolecular — interactions as the driving force in self-assembly and molecular recognition. Dimeric resorcin[4]arenes capsules have been a focus of our research for the last 15 years. This review describes the solid state complexation studies of unsubstituted phenolic resorcin[4]arenes and pyrogall[4]arenes towards the formation of dimeric capsules and assemblies using ionic and neutral species as guest molecules and templates. The multitude of different crystal structures obtained during these studies demonstrates the versatile nature of resorcin[4]arenes and pyrogall[4]arenes (2-hyd…

Molecular recognitionHydrogen bondChemistryPolymer chemistrySupramolecular chemistryIonic bondingOrganic chemistryMoleculeGeneral ChemistrySelf-assemblyCrystal structureCrystal engineeringta116Israel Journal of Chemistry
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Recent advances in aptamer-based miniaturized extraction approaches in food analysis

2021

Abstract Sample preparation is a relevant step in food analysis to achieve adequate extraction and preconcentration of target analytes before their introduction in the analytical system. Current trends in sample preparation involve moving towards miniaturized extraction devices combined with advanced affinity-based sorbents. Within affinity-based materials, aptamer-based ones have attracted much attention due to their excellent molecular recognition properties, high stability, and the possibility of immobilization onto the surface of different supporting materials, such as nanoparticles, monolithic stationary phases, etc. This review gives an overview of the literature published regarding a…

Molecular recognitionMaterials scienceAptamer010401 analytical chemistryExtraction (chemistry)New materialsNanotechnologySample preparation01 natural sciencesSpectroscopyFood Analysis0104 chemical sciencesAnalytical ChemistryTrAC Trends in Analytical Chemistry
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Smart Materials for Solid-Phase Extraction Applications

2019

Molecular recognitionMaterials scienceSorbentlawAptamerMolecularly imprinted polymerNanotechnologyCarbon nanotubeSolid phase extractionImmunosorbentsSmart materiallaw.invention
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Phycocyanobilin in solution – a solvent triggered molecular switch

2014

We present a computational investigation of the conformational response of phycocyanobilin (PCB) to the ability of solvents to form hydrogen bonds. PCB is the chromophore of several proteins in light harvesting complexes. We determine the conformational distributions in different solvents (methanol and hexamethylphosphoramide HMPT) by means of ab initio molecular dynamics simulations and characterize them via ab initio calculations of NMR chemical shift patterns. The computed trajectories and spectroscopic fingerprints illustrate that the energy landscape is very complex and exhibits various conformations of similar energy. We elucidate the strong influence of the solvent characteristics on…

Molecular switchMagnetic Resonance SpectroscopyMethanolPhycocyaninGeneral Physics and AstronomyEnergy landscapeHydrogen BondingChromophore540HempaPhotochemistrySolutionschemistry.chemical_compoundMolecular recognitionIsomerismHexamethylphosphoramidechemistryPhycocyanobilinPhycobilinsMoleculePhysical and Theoretical ChemistryProtic solventPhys. Chem. Chem. Phys.
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Small molecule inhibitors of Apaf-1-related caspase- 3/-9 activation that control mitochondrial-dependent apoptosis

2006

10 pages, 5 figures.-- PMID: 16341125 [PubMed].-- Available online Dec 9, 2005.

Multiprotein complexCytochromeProtein-protein interactionsApoptosisCaspase 3MitochondrionLigandsCell LineChemical librarychemistry.chemical_compoundPeptide LibraryApoptosomesPeptoidHumansCombinatorial libraries inhibitorApoptosomeProtein PrecursorsMolecular BiologybiologyCaspase 3Intrinsic apoptosisCytochromes cCell BiologyCaspase InhibitorsCaspase 9Recombinant ProteinsMitochondriaCell biologyEnzyme ActivationCaspasa-9Apoptotic Protease-Activating Factor 1chemistryBiochemistryN-substituted GlycinesApoptosisCaspasa-3biology.proteinApoptosomeApaf-1Molecular recognitionSmall moleculeProtein BindingCell Death & Differentiation
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Triazolopyridines. Part 28. The ring–chain isomerization strategy: triazolopyridine- and triazoloquinoline–pyridine based fluorescence ligands

2012

Abstract The ring–chain isomerization of [1,2,3]triazolo[1,5-a]pyridines or [1,2,3]triazolo[1,5-a] quinolines has been efficiently employed as a tool to provide tridentate fluorescent structures. Based on these scaffolds, a new family of highly fluorescent compounds has been synthesized and evaluated for the recognition of zinc or copper cations. In addition, the 1:1 Zn+2-L complex of a naphthalene triazolopyridine–pyridine derivative revealed high efficiency as sensor for anions providing large binding constants for nitrite and cyanide.

Nitrile[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryLigandStereochemistryCyanideOrganic Chemistry010402 general chemistry01 natural sciencesBiochemistryChemical synthesisCombinatorial chemistry0104 chemical scienceschemistry.chemical_compoundMolecular recognitionchemistryDrug DiscoveryPyridineTriazolopyridineIsomerizationTetrahedron
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Two components organogels as molecular recognition systems: properties, behavior and future applications

Organogels diimidazolium salts molecular recognition
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