Search results for "Phosphorous acid"

showing 10 items of 13 documents

Mesoporous aluminum phosphite

2009

Abstract High surface area pure mesoporous aluminum-phosphorus oxide-based derivatives have been synthesized through an S+I− surfactant-assisted cooperative mechanism by means of a one-pot preparative procedure from aqueous solution and starting from aluminum atrane complexes and phosphoric and/or phosphorous acids. A soft chemical extraction procedure allows opening the pore system of the parent as-prepared materials by exchanging the surfactant without mesostructure collapse. The nature of the pore wall can be modulated from mesoporous aluminum phosphate (ALPO) up to total incorporation of phosphite entities (mesoporous aluminum phosphite), which results in a gradual evolution of the acid…

Aqueous solutionInorganic chemistryOxideCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsInorganic ChemistryTemplate reactionMesoporous organosilicachemistry.chemical_compoundAtranechemistryMaterials ChemistryCeramics and CompositesPhysical and Theoretical ChemistryPhosphorous acidMesoporous materialPhosphoric acidJournal of Solid State Chemistry
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Optimizing the H3PO4 leaching conditions of post-precipitated sewage sludge using response surface methodology

2018

The leaching procedure of post-precipitated aluminium phosphate sludge with dilute phosphoric acid was developed. The leaching offers a route to recover both critical phosphorous from sewage sludge and the metal used in precipitation. Using phosphoric acid as leaching solution makes it possible to continue the recovery process without the need to remove chloride or sulfate anions. The optimization of the leaching was based on experimental three-level-four-variable central composite face-centered design. The four variables included were acid concentration, volume of acid, temperature and time of leaching. The leaching was conducted for dewatered and water-containing sludge (total solid conte…

Environmental EngineeringCentral composite designphosphorus recovery010501 environmental sciencesManagement Monitoring Policy and Law010403 inorganic & nuclear chemistry01 natural sciencesChloridejätevesilietechemistry.chemical_compoundmedicinePhosphorous acidSulfatecentral composite designta116ta215fosforiWaste Management and DisposalPhosphoric acidta2180105 earth and related environmental sciencessaostussewage sludgefosfaatitpost-precipitationGeneral MedicinePulp and paper industryPhosphate0104 chemical sciencestalteenottochemistryliuotusLeaching (metallurgy)Sludgemedicine.drugJournal of Environmental Management
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Scandium(III) complexes of monophosphorus acid DOTA analogues: a thermodynamic and radiolabelling study with 44 Sc from cyclotron and from a 44 Ti/ 4…

2015

International audience; The complexation ability of DOTA analogs bearing one methylenephosphonic (DO3AP) or methylene-phosphinic (DO3AP PrA and DO3AP ABn) acid pendant arm toward scandium was evaluated. Stability constants of their scandium(III) complexes were determined by potentiometry combined with 45 Sc NMR spectroscopy. The stability constants of the monophosphinate analogues are somewhat lower than that of the Sc–DOTA complex. The phosphorus acid moiety interacts with trivalent scandium even in very acidic solutions forming out-of-cage complexes; the strong affinity of the phosphonate group to Sc(III) precludes stability constant determination of the Sc–DO3AP complex. These results we…

MaleBiodistributionMagnetic Resonance SpectroscopyPhosphorous AcidsInorganic chemistrychemistry.chemical_elementPhosphorus acid[SDV.CAN]Life Sciences [q-bio]/Cancer010402 general chemistryLigands01 natural sciencesInorganic Chemistrychemistry.chemical_compoundHeterocyclic Compounds 1-Ring[SDV.CAN] Life Sciences [q-bio]/CancerOrganometallic CompoundsDOTAAnimalsScandiumPhosphorous acidRats WistarRadioisotopesTitaniumMolecular Structure010405 organic chemistryNuclear magnetic resonance spectroscopyPhosphonate0104 chemical sciencesRatschemistryStability constants of complexesPotentiometryThermodynamicsScandium
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Hopping Conductivity in Hydrogen-Bonded Antiferroelectric Compounds

1991

Antiferroelectric betaine phosphate (BP: (CH3)3NCH2COO · H3PO4) and ferroelectric betaine phosphite (BPI: (CH3)3NCH2COO · H3PO3) are molecular crystals of the amino acid betaine and the phosphoric or phosphorous acids, respectively. In both compounds the inorganic components are linked by hydrogen bonds to one-dimensional chains. The two isostructural compounds form solid solutions BPxBPI1-x at any concentration. Here we report measurements of the dielectric permittivity for concentrations 0.85 ≤ × ≤ 1 at frequencies 10−2 ≤ v ≤ 109 Hz and temperatures 2 K ≤ T ≤ 300 K. The dielectric response in BP:BPI (x = 0.95) is dominated by contributions from pure hopping conductivity which we ascribe t…

Materials scienceHydrogenHydrogen bondGeneral Chemical Engineeringchemistry.chemical_elementDielectricConductivitychemistry.chemical_compoundCrystallographyBetainechemistryPhosphorous acidIsostructuralSolid solutionBerichte der Bunsengesellschaft für physikalische Chemie
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Phosphonic Acid Analogs of Fluorophenylalanines as Inhibitors of Human and Porcine Aminopeptidases N: Validation of the Importance of the Substitutio…

2020

International audience; A library of phosphonic acid analogs of phenylalanine substituted with fluorine, chlorine and trifluoromethyl moieties on the aromatic ring was synthesized and evaluated for inhibitory activity against human (hAPN) and porcine (pAPN) aminopeptidases. Fluorogenic screening indicated that these analogs are micromolar or submicromolar inhibitors, both enzymes being more active against hAPN. In order to better understand the mode of the action of the most active compounds, molecular modeling was used. It confirmed that aminophosphonic portion of the enzyme is bound nearly identically in the case of all the studied compounds, whereas the difference in activity results fro…

Models MolecularMolecular modelPhosphorous AcidsSwineStereochemistrylcsh:QR1-502chemistry.chemical_elementPhenylalanine[CHIM.THER]Chemical Sciences/Medicinal ChemistryCD13 AntigensRing (chemistry)Biochemistrylcsh:MicrobiologyArticle03 medical and health scienceschemistry.chemical_compound0302 clinical medicinefluorineinhibitorsChlorineSide chainAnimalsHumansMolecular BiologyEnzyme Assays030304 developmental biologyphosphonic acid analogschemistry.chemical_classification0303 health sciencesTrifluoromethyl[CHIM.ORGA]Chemical Sciences/Organic chemistrymolecular modelingReproducibility of ResultsStereoisomerismMolecular Docking SimulationEnzymechemistry030220 oncology & carcinogenesishuman and porcine aminopeptidaseEnantiomerMolecules
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Synthesis and Inhibitory Studies of Phosphonic Acid Analogues of Homophenylalanine and Phenylalanine towards Alanyl Aminopeptidases.

2020

A library of novel phosphonic acid analogues of homophenylalanine and phenylalanine, containing fluorine and bromine atoms in the phenyl ring, have been synthesized. Their inhibitory properties against two important alanine aminopeptidases, of human (hAPN, CD13) and porcine (pAPN) origin, were evaluated. Enzymatic studies and comparison with literature data indicated the higher inhibitory potential of the homophenylalanine over phenylalanine derivatives towards both enzymes. Their inhibition constants were in the submicromolar range for hAPN and the micromolar range for pAPN, with 1-amino-3-(3-fluorophenyl) propylphosphonic acid (compound 15c) being one of the best low-molecular inhibitors …

Models MolecularProtein Conformation alpha-HelicalMolecular modelStereochemistryPhosphorous AcidsSwinePhenylalaninelcsh:QR1-502PhenylalanineCD13 Antigenscomputer-aided simulationsInhibitory postsynaptic potential01 natural sciencesBiochemistrylcsh:MicrobiologyArticlePhenylalanine derivativesSubstrate SpecificitySmall Molecule Libraries03 medical and health sciencesStructure-Activity RelationshipAnimalsHumansProtein Interaction Domains and MotifsEnzyme Inhibitorsphosphonic acid inhibitorsMolecular Biology030304 developmental biologyAlaninechemistry.chemical_classification0303 health sciencesInhibitory potentialBinding Sites010405 organic chemistryChemistryAminobutyratesFluorineBromine0104 chemical sciencesIsoenzymesKineticsEnzymehuman and porcine alanine aminopeptidasefluorine and bromine substitutionThermodynamicsProtein Conformation beta-StrandProtein BindingBiomolecules
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Substituted phosphonic analogues of phenylglycine as inhibitors of phenylalanine ammonia lyase from potatoes.

2018

A series of phosphonic acid analogues of phenylglycine variously substituted in phenyl ring have been synthesized and evaluated for their inhibitory activity towards potato l-phenylalanine ammonia lyase. Most of the compounds appeared to act as moderate (micromolar) inhibitors of the enzyme. Analysis of their binding performed using molecular modeling have shown that they might be bound either in active site of the enzyme or in the non-physiologic site. The latter one is located in adjoining deep site nearby the to the entrance channel for substrate into active site.

Models MolecularaminophosphonatesMolecular modelStereochemistryPhosphorous AcidsGlycinePhenylalanine ammonia-lyase010402 general chemistryRing (chemistry)01 natural sciencesBiochemistryAmmoniachemistry.chemical_compoundStructure-Activity RelationshipPAL inhibitorsEnzyme InhibitorsPhenylalanine Ammonia-LyaseSolanum tuberosumchemistry.chemical_classificationbiologymolecular modeling010405 organic chemistryActive siteSubstrate (chemistry)General MedicineLyase0104 chemical sciencesEnzymechemistrybiology.proteinBiochimie
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Stereoselective synthesis of 1-aminoalkanephosphonic acids with two chiral centers and their activity towards leucine aminopeptidase

2003

The stereoselective synthesis of 1-amino-2-alkylalkanephosphonic acids, namely, compounds bearing two chiral centers, was achieved by the condensation of hypophosphorous acid salts of (R)(+) or (S)(-)-N-alpha-methylbenzylamine with the appropriate aldehydes in isopropanol. Simultaneous deprotection and oxidation by the action of bromine water provided equimolar mixtures of the RS:RR and SR:SS diastereomers of desired acids. They appeared to act as moderate inhibitors of kidney leucine aminopeptidase with potency dependent on the absolute configuration of both centers of chirality.

PharmacologyHypophosphorous acidChemistryStereochemistryOrganic ChemistryOrganophosphonatesDiastereomerAbsolute configurationMetalloendopeptidasesStereoisomerismStereoisomerismAminopeptidaseCatalysisAnalytical Chemistry2-PropanolLeucyl AminopeptidaseZincchemistry.chemical_compoundModels ChemicalDrug DiscoveryStereoselectivityLeucineChirality (chemistry)SpectroscopyChirality
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Self-assembled monolayers based spintronics: from ferromagnetic surface functionalization to spin-dependent transport.

2016

Chemically functionalized surfaces are studied for a wide range of applications going from medicine to electronics. Whereas non-magnetic surfaces have been widely studied, functionalization of magnetic surfaces is much less common and has almost never been used for spintronics applications. In this article we present the functionalization of La2/3Sr1/3MnO3, a ferromagnetic oxide, with self-assembled monolayers for spintronics. La2/3Sr1/3MnO3 is the prototypical half-metallic manganite used in spintronics studies. First, we show that La2/3Sr1/3MnO3 can be functionalized by alkylphosphonic acid molecules. We then emphasize the use of these functionalized surfaces in spintronics devices such a…

Phosphorous AcidsSurface PropertiesElectrical Equipment and SuppliesNanotechnologyElectrons02 engineering and technology010402 general chemistry01 natural sciencesMolecular engineeringLanthanumMonolayerGeneral Materials ScienceAlkylchemistry.chemical_classificationSpintronicsMagnetic PhenomenaSelf-assembled monolayerOxides021001 nanoscience & nanotechnologyCondensed Matter Physics3. Good health0104 chemical sciencesTunnel magnetoresistancechemistryFerromagnetismManganese CompoundsStrontiumMagnetsSurface modification0210 nano-technologyJournal of physics. Condensed matter : an Institute of Physics journal
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A structural insight into the P1 S1 binding mode of diaminoethylphosphonic and phosphinic acids, selective inhibitors of alanine aminopeptidases

2016

Abstract N′-substituted 1,2-diaminoethylphosphonic acids and 1,2-diaminoethylphosphinic dipeptides were explored to unveil the structural context of the unexpected selectivity of these inhibitors of M1 alanine aminopeptidases (APNs) versus M17 leucine aminopeptidase (LAP). The diaminophosphonic acids were obtained via aziridines in an improved synthetic procedure that was further expanded for the phosphinic pseudodipeptide system. The inhibitory activity, measured for three M1 and one M17 metalloaminopeptidases of different sources (bacterial, human and porcine), revealed several potent compounds (e.g., K i  = 65 nM of 1u for Hs APN). Two structures of an M1 representative (APN from Neisser…

Phosphorous AcidsSwineStereochemistryNeisseria meningitidisCD13 AntigensCrystallography X-RayLigands010402 general chemistry01 natural sciencesAminopeptidaseArticleAminopeptidase NPhosphonic and phosphinic acidsLeucyl AminopeptidaseStructure-Activity RelationshipS1 binding modeDrug DiscoveryAnimalsHumansProtease InhibitorsPharmacologyAlanineBinding Sitesbiology010405 organic chemistryChemistryAminopeptidase NOrganic ChemistryActive siteStructural contextAPN-inhibitor complex structuresDipeptidesGeneral MedicinePhosphinic Acids0104 chemical sciencesMetalloaminopeptidasesPhosphinic Acidsbiology.proteinLeucineSelectivityEuropean Journal of Medicinal Chemistry
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