Search results for "Complexe"

showing 10 items of 920 documents

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
researchProduct

Polarimetry as a useful tool for the study of binding equilibria between cyclodextrins and some suitably sized and structured organic molecules

Settore CHIM/06 - Chimica OrganicaCyclodextrin host-guest complexes polarimetry
researchProduct

Polarimetric study of binding equilibria between cyclodextrins and some suitable organic guests

Settore CHIM/06 - Chimica OrganicaCyclodextrins host-guest complexes polarimetry
researchProduct

Binding properties of polyaminocyclodextrin materials towards polyanions and p-nitroaniline derivatives

Settore CHIM/06 - Chimica OrganicaCyclodextrins host-guest complexes supramolecula chemistry
researchProduct

On some recent investigations of probability in group theory

2010

We describe some recent contributions on the probability of commuting pairs, introduced by P. Erdos, W. Gustafson and P. Turan around 1968 and 1973. Both combinatorial methods and character theory have significant application in this context and we illustrate some standard techniques and strategies, once generalizations of the probability of commuting pairs want to be studied. The importance of the subject is emphasized in some remarks and open questions, which reformulate some classical conjectures in group theory via a probabilistic approach.

Settore MAT/02 - AlgebraSettore MAT/05 - Analisi MatematicaSettore MAT/03 - Geometriaprobability of commuting pairs complexes
researchProduct

Transporter (TAP)- and proteasome-independent presentation of a melanoma-associated tyrosinase epitope.

2000

The melanosomal protein tyrosinase is considered as a target of specific immunotherapy against melanoma. Two tyrosinase-derived peptides are presented in association with HLA-A2.1 [Wolfel et al., Eur. J. Immunol., 24, 759-764 (1994)]. Peptide 1-9 (MLLAVLYCL) is generated from the putative signal sequence. The internal peptide 369-377 is posttranslationally converted at residue 371, and its presentation is dependent on functional TAP transporters and proteasomes [Mosse et al., J. exp. Med.187, 37-48 (1998)]. Herein, we report on the processing and transport requirements for the signal sequence-derived peptide 1-9 that were studied in parallel to those for peptide 369-377. After infection of …

Signal peptideCancer ResearchProteasome Endopeptidase ComplexLactacystinAntigen presentationTyrosinase PeptidePeptideBiologyProtein Sorting SignalsEpitopechemistry.chemical_compoundEpitopesMultienzyme ComplexesHLA-A2 AntigenTumor Cells CulturedHumansATP Binding Cassette Transporter Subfamily B Member 2Melanomachemistry.chemical_classificationAntigen PresentationMonophenol MonooxygenaseCell biologyCTL*Cysteine EndopeptidasesOncologychemistryProteasomeBiochemistryATP-Binding Cassette TransportersT-Lymphocytes CytotoxicInternational journal of cancer
researchProduct

Reactivity of antitumor coinage metal-based N-heterocyclic carbene complexes with cysteine and selenocysteine protein sites

2021

Abstract The reaction of the antitumor M(I)-bis-N-heterocyclic carbene (M(I)-NHC) complexes, M = Cu, Ag, and Au, with their potential protein binding sites, i.e. cysteine and selenocysteine, was investigated by means of density functional theory approaches. Capped cysteine and selenocysteine were employed to better model the corresponding residues environment within peptide structures. By assuming the neutral or deprotonated form of the side chains of these amino acids and by considering the possible assistance of an external proton donor such as an adjacent acidic residue or the acidic component of the surrounding buffer environment, we devised five possible routes leading to the binding o…

SilverAnticancer; Copper(I) complexes; DFT calculations; Gold(I) complexes; N-heterocyclic carbenes; Silver(I) complexesStereochemistryCoinage metalsAntineoplastic AgentsProtonationLigandsDFT calculationsBiochemistrySilver(I) complexesInorganic Chemistrychemistry.chemical_compoundDeprotonationProtein structureCoordination ComplexesCysteineN-heterocyclic carbenesDensity Functional Theorychemistry.chemical_classificationMolecular StructureSelenocysteineCopper(I) complexesSelenocysteineAmino acidAnticancerGold(I) complexesModels ChemicalchemistryThermodynamicsGoldCarbeneCopperCysteineJournal of Inorganic Biochemistry
researchProduct

Catalytic Functionalization of Methane and Light Alkanes in Supercritical Carbon Dioxide

2014

International audience; The development of catalytic methods for the effective functionalization of methane yet remains a challenge. The best system known to date is the so-called Catalytica Process based on the use of platinum catalysts to convert methane into methyl bisulfate with a TOF rate of 10−3 s. In this contribution, we report a series of silver complexes containing perfluorinated tris(indazolyl)borate ligands that catalyze the functionalization of methane into ethyl propionate upon reaction with ethyl diazoacetate (EDA) by using supercritical carbon dioxide (scCO2) as the reaction medium. The employment of this reaction medium has also allowed the functionalization of ethane, prop…

SilverLigands010402 general chemistry01 natural sciences7. Clean energyCatalysisCatalysischemistry.chemical_compoundEthyl propionateEthyl diazoacetateCoordination ComplexesMethyl bisulfateAlkanesOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistrySupercritical carbon dioxide010405 organic chemistryOrganic ChemistryButaneDiazonium CompoundsGeneral ChemistryCarbon Dioxide0104 chemical sciencesSolubilitychemistryIsobutaneOxidative coupling of methaneMethaneChemistry - A European Journal
researchProduct

Monolacunary Keggin polyoxometalates connected to ten 4d or 4f metal atoms.

2013

The rational self-assembly of mono-lacunary Keggin clusters with 4d and 4f metal salts via a conventional method has yielded two novel polyoxometalate-based 4d-4f heterometallic compounds containing lacunary Keggin anions connected to ten metal atoms: {[Ag{Ag2(H2O)4}{Ln(H2O)6}2H ⊂ {SiW11Ln(H2O)4O39}2]·nH2O (Ln = Ce and n = 7 for 1, Ln = Pr and n = 3 for 2). Their structures were determined by single crystal X-ray diffraction analyses and further characterized by elemental analyses, IR spectra, and thermogravimetric (TG) analyses. A structural feature in 1 and 2 is that each [SiW11O39](8-) cluster (SiW11) is connected to ten metals (five Ag(+) and five Ln(3+) cations), representing the highe…

SilverMagnetic momentMolecular StructureChemistryMagnetic PhenomenaInorganic chemistryInfrared spectroscopyCeriumTungsten CompoundsCrystallography X-RayIonInorganic ChemistryMetalCrystallographyX-Ray DiffractionCoordination Complexesvisual_artPolyoxometalateThermogravimetryCluster (physics)visual_art.visual_art_mediumPraseodymiumLacunary functionSingle crystalDalton transactions (Cambridge, England : 2003)
researchProduct

Reinvestigation of the Pd-catalysed bis(silylation) of alkynes with 1,1,2,2-tetramethyl-1,2-bis(phenylthiomethyl)disilane: Unexpected formation of th…

2013

International audience; The bis(silylated) alkenes Z-(PhSCH2)Me2SiC(H)=C(Fc)SiMe2(CH2SPh) (2) and Z-(PhSCH2)Me2SiC(H)=C(bipheny)SiMe2(CH2SPh) (3) have been prepared by Pd-catalysed double silylation of ethynylferrocene and 4-ethynyl-1,1'-biphenyl in the presence of 1,1,2,2-tetramethyl-1,2-bis(phenylthiomethyl)disilane (1). A reinvestigation on the interaction of 1 with [PdCl2(PhCN)2] in technical-grade CH2Cl2 as solvent revealed competition between reduction to elemental palladium (due to oxidative addition of the Si-Si bond across Pd(II) and subsequent reductive elimination) and formation of an unusual eight-membered chelate complex cis-[PdCl2{(PhSCH2SiMe2)2O}] (4), which is fluxional in s…

SilylationStereochemistryEthynylferrocene[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryDFTReductive eliminationInorganic Chemistrychemistry.chemical_compound[ CHIM.CRIS ] Chemical Sciences/Cristallography[ CHIM.ORGA ] Chemical Sciences/Organic chemistryDisilaneMaterials Chemistry[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryConformational isomerismComputingMilieux_MISCELLANEOUSThioether complexesSiloxane010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryDisiloxaneOxidative addition0104 chemical scienceschemistrySiloxaneDisilanePalladium
researchProduct