Search results for "Chela"

showing 10 items of 415 documents

Evidence for Three Distinct Classes of Phenotype Severity in Beta-Thalassaemia

2019

Background: Classification of phenotype severity in patients with beta-thalassaemia has so far relied mainly on expert opinion using parameters of genotype, clinical features at diagnosis, and transfusion requirement. The aim of this study was to use a large dataset of patients with beta-thalassaemia and evaluate a classification system based on onset variables agreed on by an international expert group, including age at diagnosis, at first transfusion, and at first iron chelation. Methods: A retrospective dataset of 7910 patients with homozygous or compound heterozygous beta-thalassaemia was used and subjected to cluster and classification analysis starting with the onset variables. Result…

medicine.medical_specialtyHeart diseasebusiness.industryCompound heterozygositymedicine.diseasePhenotypeIron chelationBeta-thalassaemiaInternal medicineHepatocellular carcinomaGenotypeMedicinebusinessProspective cohort studySSRN Electronic Journal
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Copper(II) and nickel(II) chelates with dihydrogen Trans-1,2-diaminocyclohexane-N,N,N′,N′-tetraacetate(2−) ion (H2CDTA2−). Synthesis, XRD structure a…

1996

Abstract Stoichiometric reactions of metal hydroxycarbonates with the acid trans -1,2-cyclohexanediaminotetraacetic acid (H 4 CDTA) in water under reduced pressure yielded [Cu(H 2 CDTA)]·H 2 O ( I ) and [Ni(H 2 CDTA) (H 2 O)]·4H 2 O ( II ). Both compounds were characterized by TG-DTA analysis, spectral properties (IR, reflectance and RSE) and X-ray diffraction. In I the copper(II) atom exhibits a distorted square-base coordination (type 4+1) by chelation of one H 2 CDTA 2− ligand through two N and two O (carboxylate) at the square base and one O (carboxylic) at the apex of the coordination polyhedron; a second carboxymethyl group of H 2 CDTA 2− remains free. In II the H 2 CDTA 2− chelating …

Ligandtrans-12-Diaminocyclohexanechemistry.chemical_elementProtonationInorganic ChemistryMetalchemistry.chemical_compoundNickelCrystallographychemistryOctahedronvisual_artMaterials Chemistryvisual_art.visual_art_mediumChelationCarboxylatePhysical and Theoretical ChemistryPolyhedron
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Influence of the Nature of the Ligand on Dirhodium(II) Carbene Species: A Theoretical Analysis

2008

The influence of three prototypic families of bridging ligands (carboxylate, carboxamidate, and ortho-metalated arylphosphines) on the electronic structure of dirhodium(II) carbene complexes was theoretically analyzed. The calculations indicated that the electron donation of the ligand to the Rh atom, rather than the chelating ability or the metal−ligand orbital mixing, was responsible for tuning carbene charge via back-donation, which can influence the reactivity and selectivity of the dirhodium complexes in catalytic carbene transfer reactions.

LigandStereochemistryOrganic ChemistryElectronic structureMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryChelationCarboxylatePhysical and Theoretical ChemistrySelectivityCarbeneOrganometallics
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Effect of chelatants on gellan gel rheological properties and setting temperature for immobilization of living bifidobacteria.

1993

The effect of various concentrations of sequestrants (sodium citrate, sodium metaphosphate, and EDTA) was studied on gellan gel (1.5-2.5% (w/v)) setting temperature and rheological properties. Addition of EDTA between 0 and 0.8% (w/v) led to a progressive decrease of setting temperature. Citrate and metaphosphate decreased this parameter when added up to 0.4 or 0.6%, depending on gellan gum concentration, eventually resulting in the absence of gel formation at room temperature for the 1.5% gellan solution containing 0.4% citrate. This effect was accompanied by a significant decrease of gel strength and stiffness and might be attributed to the binding of the divalent cations required for cha…

chemistry.chemical_classificationBifidobacterium longumChromatographybiologyMetaphosphatePolysaccharides BacterialTemperatureConcentration effectHydrogen-Ion ConcentrationPolysaccharidebiology.organism_classificationGellan gumLactic acidCulture Mediachemistry.chemical_compoundchemistryCell MovementSodium citrateFermentationBifidobacteriumRheologyGelsBiotechnologyChelating AgentsBiotechnology progress
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Pharmacological Suppression of CNS Scarring by Deferoxamine Reduces Lesion Volume and Increases Regeneration in an In Vitro Model for Astroglial-Fibr…

2015

Lesion-induced scarring is a major impediment for regeneration of injured axons in the central nervous system (CNS). The collagen-rich glial-fibrous scar contains numerous axon growth inhibitory factors forming a regeneration-barrier for axons. We demonstrated previously that the combination of the iron chelator 2,2'-bipyridine-5,5'-decarboxylic acid (BPY-DCA) and 8-Br-cyclic AMP (cAMP) inhibits scar formation and collagen deposition, leading to enhanced axon regeneration and partial functional recovery after spinal cord injury. While BPY-DCA is not a clinical drug, the clinically approved iron chelator deferoxamine mesylate (DFO) may be a suitable alternative for anti-scarring treatment (A…

Central Nervous SystemCollagen Type IVmedicine.medical_specialtyNeuriteCentral nervous systemlcsh:MedicineBiologyPharmacologyDeferoxamineIn Vitro TechniquesIron Chelating AgentsCicatrixIn vivoTransforming Growth Factor betamedicineCyclic AMPNeuritesAnimalsHumansRNA MessengerAxonRats Wistarlcsh:ScienceSpinal cord injurySpinal Cord InjuriesMultidisciplinaryDeferoxamine mesylatelcsh:RFibroblastsSpinal cordmedicine.diseaseAxonsSurgeryNerve RegenerationRatsDeferoxamineDisease Models Animalmedicine.anatomical_structureAstrocyteslcsh:QFemalemedicine.drugResearch ArticlePloS one
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Titanium Complexes Stabilized by a Sulfur‐Bridged Chelating Bis(aryloxo) Ligand as Active Catalysts for Olefin Polymerization

2004

The mixed-ligand complexes [Ti2(μ-OR)2(OR)2(κ3-tbop)2] (1a) for R = Me and (1b) R = Et were prepared by the reaction of Ti(OR)4 and H2tbop {H2tbop = 2,2′-thiobis[4-(1,1,3,3-tetramethylbutyl)phenol]} in methanol. Treatment of 1a and 1b with AlMe3 led to the substitution of terminal alkoxy groups to create the organometallic compounds [Ti2(μ-OR)2(κ3-tbop)2(Me)2] (2a) for R = Me and (2b) for R = Et. Controlled hydrolysis of 2b causes the evolution of methane and the formation of the titanoxane compounds [{Ti2(μ-OEt)2(κ3-tbop)2}2(μ-O)2]·2CH2Cl2 (3). Structures of 1a, 1b, 2a, 2b, and 3 were confirmed by NMR spectroscopy; 1b and 3 were further investigated with X-ray crystallography. Compounds 1a…

TitaniumEthyleneLigandSONuclear magnetic resonance spectroscopyCatalysisPolymerizationInorganic Chemistrychemistry.chemical_compoundO ligandschemistryPolymerizationPolymer chemistryAlkoxy groupChelationX‐ray diffractionGroup 2 organometallic chemistryAluminumEuropean Journal of Inorganic Chemistry
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Synthesis and preliminary in vivo evaluation of well-dispersed biomimetic nanocrystalline apatites labeled with positron emission tomographic imaging…

2015

In recent years, biomimetic synthetic apatite nanoparticles (AP-NPs), having chemical similarity with the mineral phase of bone, have attracted a great interest in nanomedicine as potential drug carriers. To evaluate the therapeutic perspectives of AP-NPs through the mechanisms of action and organs they interact with, the noninvasive monitoring of their in vivo behavior is of paramount importance. To this aim, here the feasibility to radiolabel AP-NPs ("naked" and surface-modified with citrate to reduce their aggregation) with two positron emission tomographic (PET) imaging agents ([F-18]NaF and Ga-68-NO(2)AP(BP)) was investigated. [F-18]NaF was used for the direct incorporation of the radi…

inorganic chemicalsMalepositron emission tomographyMaterials scienceNanoparticleNanotechnologyPilot ProjectsDiffusionNanocapsulesIn vivoBiomimetic MaterialsApatitesMaterials TestingmedicineAnimalsGeneral Materials ScienceChelationWhole Body ImagingColloidsParticle SizeRats Wistarmedicine.diagnostic_testtechnology industry and agriculturenanomedicinecalcium phosphatesPositron emission tomographyIsotope LabelingPositron-Emission Tomographydrug deliveryDrug deliverySurface modificationNanomedicineFeasibility StudiesNanoparticlesRadiopharmaceuticalsDrug carrierCrystallizationACS applied materialsinterfaces
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Dibromido[N-(1-diethylamino-1-oxo-3-phenylpropan-2-yl)-N′-(pyridin-2-yl)imidazol-2-ylidene]palladium(II) dichloromethane monosolvate

2019

In the molecule of the title N,N′-disubstituted imidazol-2-ylidene palladium(II) complex, [PdBr2(C21H24N4O)]·CH2Cl2, the palladium(II) atom adopts a slightly distorted square-planar coordination (r.m.s. deviation = 0.0145 Å), and the five-membered chelate ring is almost planar [maximum displacement = 0.015 (8) Å]. The molecular conformation is enforced by intramolecular C—H...Br hydrogen bonds. In the crystal, complex molecules and dichloromethane molecules are linked into a three-dimensional network by C—H...O and C—H...Br hydrogen bonds.

crystal structureHydrogen bondchemistry.chemical_element02 engineering and technologyGeneral MedicineCrystal structure010402 general chemistry021001 nanoscience & nanotechnologyRing (chemistry)palladium01 natural sciencesMedicinal chemistryMethane0104 chemical scienceschemistry.chemical_compoundchemistrylcsh:QD901-999Chelationlcsh:Crystallography0210 nano-technologyMaximum displacementimidazol-2-ylidenePalladiumIUCrData
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Different patterns of myocardial iron distribution by whole-heart T2* magnetic resonance as risk markers for heart complications in thalassemia major.

2014

Background The multislice multiecho T2* cardiovascular magnetic resonance (CMR) technique allows to detect different patterns of myocardial iron overload (MIO). The aim of this cross-sectional study was to verify the association between cardiac complications (heart failure and arrhythmias), biventricular dysfunction and myocardial fibrosis with different patterns of MIO in thalassemia major (TM) patients. Methods We considered 812 TM patients enrolled in the Myocardial Iron Overload in Thalassemia (MIOT) Network. The T2* value in all the 16 cardiac segments was evaluated. Results We identified 4 groups of patients: 138 with homogeneous MIO (all segments with T2* < 20 ms), 97 with heterogene…

AdultMalemedicine.medical_specialtyHeart DiseasesThalassemiaIronMyocardial ironMagnetic Resonance Imaging CineMyocardial iron overloadYoung AdultRisk FactorsInternal medicineMedicineDistribution (pharmacology)HumansMultisliceChelation therapyCardiac complicationThalassemia majormedicine.diagnostic_testbusiness.industryMyocardiumbeta-ThalassemiaMagnetic resonance imagingmedicine.diseaseCross-Sectional StudiesHeart failureCardiologyMyocardial fibrosisCardiovascular magnetic resonanceFemaleCardiology and Cardiovascular MedicinebusinessInternational journal of cardiology
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Sequence similarity of mammalian epoxide hydrolases to the bacterial haloalkane dehalogenase and other related proteins Implication for the potential…

1994

Direct comparison of the amino acid sequences of microsomal and soluble epoxide hydrolase superficially indicates that these enzymes are unrelated. Both proteins, however, share significant sequence similarity to a bacterial haloalkane dehalogenase that has earlier been shown to belong to the alpha/beta hydrolase fold family of enzymes. The catalytic mechanism for the dehalogenase has been elucidated in detail [Verschueren et al. (1993) Nature 363, 693-698] and proceeds via an ester intermediate where the substrate is covalently bound to the enzyme. From these observations we conclude (i) that microsomal and soluble epoxide hydrolase are distantly related enzymes that have evolved from a co…

Epoxide hydrolase 2StereochemistryHydrolasesMolecular Sequence DataBiophysicsHydrolaseEsteraseBiochemistryEsteraseCatalysisChelataseα/β Hydrolase foldBacterial ProteinsStructural BiologyMicrosomesHydrolaseGeneticsAnimalsAmino Acid SequenceEpoxide hydrolaseMolecular BiologyDehalogenasePeroxidasechemistry.chemical_classificationEpoxide HydrolasesMammalsBacteriaSequence Homology Amino AcidCell BiologyLipaseBiological EvolutionEnzymechemistryBiochemistrySolubilityEpoxide HydrolasesLuciferaseHaloalkane dehalogenaseFEBS Letters
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