Search results for "nicotinic acid"

showing 10 items of 21 documents

Effects of sorbinicate and nicotinic acid on blood viscosity, red cell deformation and platelet function

1982

Summary Nicotinic acid (NA) and a retard derivative, sorbinicate, were investigated for their effects on blood rheology and platelet function, after oral administration, in two groups of patients with lower limb atherosclerosis obliterans — the second group having diabetes also. Red cell deformation and blood plasma viscosity were studied in the nondiabetic group (single dose of NA, 100 mg, and sorbinicate, 400 mg); release of platelet malondialdehyde (MDA) (single dose of NA, 100 mg, and sorbinicate, 800 mg), and the platelet regeneration time (before and after sorbinicate 400 mg × 3/die for 7 days) were studied in the diabetic group. Both drugs induced a significant improvement in red cel…

AdultBlood PlateletsMalemedicine.medical_specialtyErythrocytesTime FactorsBlood viscosityNiacinchemistry.chemical_compoundNEFAOral administrationMalondialdehydeInternal medicineDiabetes mellitusBlood plasmamedicineHumansSorbitolPlateletTriglyceridesPharmacologyRed CellChemistryNicotinic AcidsFibrinogenMiddle AgedBlood Viscositymedicine.diseaseMalondialdehydeCholesterolEndocrinologyBiochemistryFemalePharmacological Research Communications
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Effect of hypolipidemic treatment on emerging risk factors in mixed dyslipidaemia: a randomized pilot tria

2013

Background The effects of different hypolipidemic treatment strategies on emerging atherosclerosis risk factors remain unknown. Materials and methods This is a prespecified analysis of a prospective, randomized, open-label, blinded end point (PROBE) study (ClinicalTrials.gov identifier: NCT01010516). Patients (n = 100) with mixed dyslipidaemia on a standard statin dose who had not achieved lipid targets were randomized to switch to the highest dose of rosuvastatin (40 mg/day) or to add-on-statin extended release nicotinic acid (ER-NA)/laropiprant (LRPT) or to add-on-statin micronized fenofibrate for a total of 3 months. Results Following 3 months of treatment, low-density lipoprotein (LDL) …

C-reactive protein fenofibrate lipoprotein-associated phospholipase A2 nicotinic acid rosuvastatin small dense low-density lipoprotein cholesterol.
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A new Co(II) coordination solid with mixed oxygen, carboxylate, pyridine and thiolate donors exhibiting canted antiferromagnetism with TC ≈ K

2006

Reaction of Co(II) chloride with the sodium salt of 2-mercaptonicotinic acid in water at 200 ºC results in the formation of Co4(2-mna)4(H2O), which orders as a canted antiferromagnet at 68 K. Gomez Garcia, Carlos Jose, Carlos.Gomez@uv.es

CoOxygenMercaptonicotinic acidCo ; Oxygen ; Carboxylate ; Pyridine ; Sodium salt ; Mercaptonicotinic acid ; AntiferromagnetPyridineUNESCO::QUÍMICACarboxylateSodium salt:QUÍMICA::Química macromolecular [UNESCO]UNESCO::QUÍMICA::Química macromolecularAntiferromagnet:QUÍMICA [UNESCO]
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Preparation and structural studies on the tBu2Sn(IV) complexes with aromatic mono- and dicarboxylic acids containing hetero {N} donor atom

2004

Nine complexes of 'Bu2Sn(IV)(2+) were obtained in the solid state with ligands containing -COOH group(s) and aromatic (N) donor atom. The binding sites of the ligands were identified by FT-IR spectroscopic measurements. It was found that in most cases the -COO- groups are co-ordinated in monodentate manner. Nevertheless, in some of our complexes, the -COO- group forms bridges between two central {Sn} atoms resulting in the formation of an oligomeric structure, a motif that is characteristic only to the nicotinate compound. These pieces of information and the rationalisation of the experimental Sn-119 Mossbauer nuclear quadrupole splittings, Delta, - according to the point charge model forma…

DenticitygeometryX ray diffractionCrystal structureOrganotin(IV)nicotinic acid derivativeBiochemistryInorganic Chemistrycomplex formationMaterials ChemistryMoleculeorganotin compoundcontrolled studyPhysical and Theoretical Chemistryinfrared spectroscopychemical bindinghydrogen bondHydrogen bondChemistryMössbauer spectroscopybinding siteOrganic ChemistryarticleSquare pyramidal molecular geometryX-ray diffractionFT-IRtin derivativeTrigonal bipyramidal molecular geometryCrystallographyOctahedrondicarboxylic acidSettore CHIM/03 - Chimica Generale E Inorganicachemical structureMolecular modellingcarboxylic acidsynthesimolecular modelchemical analysiSingle crystal
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Heme symmetry, vibronic structure, and dynamics in heme proteins: ferrous nicotinate horse myoglobin and soybean leghemoglobin.

2000

We report the visible and Soret absorption bands, down to cryogenic temperatures, of the ferrous nicotinate adducts of native and deuteroheme reconstituted horse heart myoglobin in comparison with soybean leghemoglobin-a. The band profile in the visible region is analyzed in terms of vibronic coupling of the heme normal modes to the electronic transition in the framework of the Herzberg–Teller approximation. This theoretical approach makes use of the crude Born–Oppenheimer states and therefore neglects the mixing between electronic and vibrational coordinates; however, it takes into account the vibronic nature of the visible absorption bands and allows an estimate of the vibronic side bands…

HemeproteinsHemeproteinBiophysicsHemePhotochemistryBiochemistryVibrationMolecular electronic transitionSpectral lineBiomaterialschemistry.chemical_compoundAnimalsFerrous CompoundsHorsesHemeMyoglobinProtein dynamicsOrganic ChemistryNicotinic AcidsTemperatureGeneral MedicineProtein Structure TertiaryLeghemoglobinVibronic couplingMyoglobinchemistrySpectrophotometryMolecular vibrationSoybeansBiopolymers
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Chloride–hydrogen interactions of picolinic, nicotinic and isonicotinic acid chloride hydrochlorides in the crystalline state

2003

The crystal structures of the three isomers of the chemically labile pyridinecarboxylic acid chloride hydrochlorides were analyzed in order to study the weak interactions of the chloride anion with hydrogens. The chloride anions in the crystal structure of 1a have a slightly distorted square-planar interaction sphere with four hydrogens in the equatorial plane (plane of the molecule) with Cl−⋯H distances varying from 2.041(1) A [NH+⋯Cl−] to 2.933(1) A [CH⋯Cl−]. Nicotinic and isonicotinic acid chloride hydrochloride 1b and 1c show that chloride anion has a crucial role in the formation of bridged dimeric structures. The crystal lattices of 1b and 1c manifest similar herring-bone packing patt…

HydrochlorideIntermolecular forceInorganic chemistryGeneral ChemistryCrystal structureCondensed Matter PhysicsIsonicotinic acidChlorideIonchemistry.chemical_compoundCrystallographychemistrymedicineMoleculeGeneral Materials ScienceSublimation (phase transition)medicine.drugCrystEngComm
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The structure of trinuclear Cu(II) complex with isonicotinic acid N-oxide, pentaaquadi-μ-hydroxobis-μ-(ionicotinato N-oxide)bis(isonicotinato N-oxide…

1983

Abstract A new trinuclear Cu(II) complex with isonicotinic acid N-oxide, [Cu3(N-inicO)4(OH)2(H2O)5·2H2O, has been prepared and its crystal structure determined by X-ray analysis. The complex crystallizes in the monoclinic space group P2/c with a = 12.051(4), b = 7.043(2), c = 19.825(6) A, β = 98.51(2)° and Z = 2. The arrangement of the three Cu atoms is triangular, with distances of 3.365(1) A between the central and terminal Cu atoms. The coppers are pentacoordinated; the coordination geometry is tetrahedral distorted square pyramidal for the terminal Cu atoms and elongated square pyramidal for the central Cu atom. Two hydroxo ligands and two of the four isonicotinato N-oxide ligands throu…

Inorganic Chemistrychemistry.chemical_compoundCrystallographychemistryAtomMaterials ChemistryOxideCrystal structurePhysical and Theoretical ChemistryIsonicotinic acidSquare pyramidal molecular geometryMonoclinic crystal systemCoordination geometryInorganica Chimica Acta
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Single layers of a multifunctional laminar Cu(I,II) coordination polymer.

2010

A multifunctional bidimensional mixed-valence copper coordination polymer [Cu2Br(IN)2]n (IN = isonicotinato) has been characterized in crystal phase and isolated on graphite surface as single sheets.

Models MolecularMaterials scienceCoordination polymerPolymersSurface Propertieschemistry.chemical_elementCrystallography X-RayCatalysisCrystalchemistry.chemical_compoundPhase (matter)Polymer chemistryMaterials ChemistryOrganometallic CompoundsGraphiteGroup 2 organometallic chemistrychemistry.chemical_classificationMetals and AlloysLaminar flowGeneral ChemistryPolymerCopperSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryCeramics and CompositesGraphiteIsonicotinic AcidsCopperChemical communications (Cambridge, England)
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Electrical conductivity and strong luminescence in copper Iodide double chains with isonicotinato derivatives

2015

Direct reactions between CuI and isonicotinic acid (HIN) or the corresponding esters, ethyl isonicotinate (EtIN) or methyl isonicotinate (MeIN), give rise to the formation of the coordination polymers [CuI(L)] with L=EtIN (1), MeIN (2) and HIN (3). Polymers 1-3 show similar structures based on a CuI double chain in which ethyl-, methyl isonicotinate or isonicotinic acid are coordinated as terminal ligands. Albeit, their supramolecular architecture differs considerably, affecting the distances and angles of the central CuI double chains and thereby their physical properties. Hence, the photoluminescence shows remarkable differences; 1 and 2 show a strong yellow emission, whereas 3 displays a…

Models MolecularThermogravimetric analysisPhotoluminescenceLuminescencePolymersInorganic chemistrySupramolecular chemistrychemistry.chemical_elementConductivityIsonicotinic acidLigandsNiacinCatalysisCopper iodidechemistry.chemical_compoundCoordination ComplexesElectrical conductivityCarboxylateMolecular StructureStructure elucidationOrganic ChemistryElectric ConductivityGeneral ChemistryIodidesCopperCoordination polymersCrystallographychemistryLuminescenceCopper
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The electrochemical reduction of thioisonicotinamide in an aqueous medium

1998

Abstract The electrochemical reduction of thioisonicotinamide NRCSNH 2 has been examined in an aqueous medium between H 0 =−1 and pH=13.7. As shown by cyclic voltammetry and polarography, a global 2e − reversible transfer is followed by two successive first-order chemical reactions and a 2e − , 2H + reduction (EC 1 C 2 E process). A mechanism is proposed, beginning with the 2e − reduction of NRCSNH 2 to the formal diionized form NRC − (SH)(NH 3 + ), the first chemical reaction, C 1 , being a formal proton transfer which yields the 4- gem aminosulfanylmethylpyridine; the rate constant of this reaction is 2×10 4  s −1 in acidic medium and diminishes in neutral medium. The second process, C 2 …

Reaction mechanismPolarographyAqueous solutionStereochemistryGeneral Chemical EngineeringInorganic chemistryIsonicotinic acidChemical reactionchemistry.chemical_compoundReaction rate constantchemistryElectrochemistryIsonicotinamideCyclic voltammetryElectrochimica Acta
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