Search results for "PYRIDINE"

showing 10 items of 2516 documents

New Hypolipaemic Agents Designed by Molecular Topology: Pharmacological Studies of 2,6-Di-tert-butyl-4-methylpyridine and 2,6-Di-tert-butylpyridine

1999

New compounds showing hypolipaemic activity have been designed using a computer-aided method based on molecular topology and QSAR analysis. Linear discriminant analysis and connectivity functions were used to design three potentially suitable drugs which were tested for hypolipaemic properties by the Triton WR-1339 test in rats. The pharmacological tests carried out on the newly designed compounds demonstrated the existence of notable activity in phase I for two of them. namely 2,6-Di-tert-butyl-4-methylpyridine (C.A.S. 38222-83-2) and 2,6-Di-tert-butylpyridine (C.A.S. 585-48-8), with respect to the level of total cholesterol. Both substances decrease the lipaemia to lower levels than clofi…

PharmacologyTert butylQuantitative structure–activity relationshipClofibrateChemistryStereochemistry26-Di-tert-butylpyridineReference drugchemistry.chemical_compoundTotal cholesterol4-MethylpyridinemedicineMolecular topologymedicine.drugQuantitative Structure-Activity Relationships
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Enantioselective copper-aminopyridine-catalyzed aza-Henry reaction with chelating N-(2-pyridyl)sulfonyl imines

2012

This article describes a copper-catalyzed aza-Henry reaction. Copper complexes of camphor-derived aminopyridines catalyze the addition of nitromethane to N-(2-pyridyl)sulfonyl aldimines to give the corresponding β-nitrosulfonamides with good yields and variable enantiomeric excesses (up to 83%). An example of transformation of these compounds into N-(2-pyridyl)sulfonyl-α-amino acids and deprotection of the sulfonamide with Mg–MeOH is provided. Chirality 24:441–450, 2012. © 2012 Wiley Periodicals, Inc.

Pharmacologychemistry.chemical_classificationSulfonylAldimineNitroaldol reactionNucleophilic additionOrganic ChemistryEnantioselective synthesisMedicinal chemistryCatalysisAnalytical ChemistrySulfonamidechemistryDrug DiscoveryOrganic chemistryChirality (chemistry)SpectroscopyAminopyridinesChirality
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Standard versus personalized schedule of regorafenib in metastatic gastrointestinal stromal tumors: a retrospective, multicenter, real-world study

2021

Background Despite its proven activity as third-line treatment in gastrointestinal stromal tumors (GIST), regorafenib can present a poor tolerability profile which often leads to treatment modifications and transient or permanent discontinuation; thus, in clinical practice physicians usually adopt various dosing and interval schedules to counteract regorafenib-related adverse events and avoid treatment interruption. The aim of this real-world study was to investigate the efficacy and safety of personalized schedules of regorafenib in patients with metastatic GIST, in comparison with the standard schedule (160 mg daily, 3-weeks-on, 1-week-off). Patients and methods Institutional registries a…

Phenylurea CompoundOncologyCancer Researchmedicine.medical_specialtyScheduleStromal cellPyridinesGastrointestinal Stromal TumorsPyridinePersonalized treatmentchemical and pharmacologic phenomenaMultikinase inhibitorchemistry.chemical_compoundQuality of lifeRetrospective Studieimmune system diseaseshemic and lymphatic diseasesInternal medicineRegorafenibmedicineHumansOriginal ResearchRetrospective StudiesGiSTbusiness.industryPhenylurea Compoundstoxicityhemic and immune systemspersonalized treatmentdigestive system diseasesquality of lifeOncologychemistryregorafenibGIST; personalized treatment; quality of life; regorafenib; toxicity; Humans; Phenylurea Compounds; Pyridines; Retrospective Studies; Gastrointestinal Stromal TumorsbusinessHumanGISTESMO Open
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Activity and Thermal Stability of Cobalt(II)-Based Olefin Polymerization Catalysts Adorned with Sterically Hindered Dibenzocycloheptyl Groups.

2019

Five examples of unsymmetrical 2-(2,4-bis(dibenzocycloheptyl)-6-methylphenyl- imino)ethyl)-6-(1-(arylyimino)ethyl)pyridine derivatives (aryl = 2,6-Me2C6H3 in L1

Photochemistry2Pharmaceutical Sciencechemistry.chemical_elementCatalysisArticlethermal stabilityAnalytical ChemistryPolymerizationlcsh:QD241-441chemistry.chemical_compoundDibenzocycloheptyl grouplcsh:Organic chemistryDrug DiscoveryPolymer chemistryPyridine26-bis(imino)pyridylcobalt(II) chloride precatalystsThermal stabilityPhysical and Theoretical ChemistryMolecular StructureOrganic ChemistryCobaltPolyethyleneSquare pyramidal molecular geometryLinear low-density polyethylene6-bis(imino)pyridylcobalt(II) chloride precatalystschemistryPolymerizationhigh molecular-weight saturated/unsaturated polyethyleneChemistry (miscellaneous)PolyethyleneMolecular MedicineMolar mass distributionCobaltMolecules (Basel, Switzerland)
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Solid-Phase Synthesis of Peptide Libraries Combining α-Amino Acids with Inorganic and Organic Chromophores

2009

The synthesis of two series of peptidic chains composed of bis(terpyridine)ruthenium(II) acceptor units and organic chromophores (coumarin, naphthalene, anthracene, fluorene) by stepwise solid-phase peptide synthesis (SPPS) techniques is described. The first series of dyads comprises directly amide linked chromophores, while the second one possesses a glycine spacer between the two chromophores. All dyads were studied by UV/Vis and NMR spectroscopy, steady-state luminescence, luminescence decay and electrochemistry, as well as by DFT calculations. The results of these studies indicate weak electronic coupling of the chromophores in the ground state. Absorption spectra of all dyads are domin…

Photochemistrychemistry.chemical_elementNaphthalenesFluorenePhotochemistryRutheniumCatalysischemistry.chemical_compoundCoumarinsPeptide LibraryElectrochemistryAmino AcidsColoring AgentsAnthracenesFluorenesAnthraceneQuenching (fluorescence)Spectrum AnalysisOrganic ChemistryGeneral ChemistryNuclear magnetic resonance spectroscopyChromophoreRutheniumchemistryTerpyridinePeptidesLuminescenceChemistry - A European Journal
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Thienylpyridine-based cyclometallated iridium(III) complexes and their use in solid state light-emitting electrochemical cells

2013

The synthesis and characterization of four iridium(iii) complexes [Ir(thpy)2(N^N)][PF6] where Hthpy = 2-(2'-thienyl)pyridine and N^N are 6-phenyl-2,2'-bipyridine (1), 4,4'-di-(t)butyl-2,2'-bipyridine (2), 4,4'-di-(t)butyl-6-phenyl-2,2'-bipyridine (3) or 4,4'-dimethylthio-2,2'-bipyridine (4) are described. The single crystal structures of ligand 4 and the complexes containing the [Ir(thpy)2(1)](+) and [Ir(thpy)2(4)](+) cations have been determined. In [Ir(thpy)2(1)](+), the pendant phenyl ring engages in an intra-cation π-stacking interaction with one of the thienyl rings in the solid state, and undergoes hindered rotation on the NMR timescale in [Ir(thpy)2(1)](+) and [Ir(thpy)2(3)](+). The …

PhotoluminescenceLigandAnalytical chemistrychemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesSpectral line0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryPyridineDensity functional theoryIridiumEmission spectrum0210 nano-technologySingle crystal
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Fluorine-free blue-green emitters for light-emitting electrochemical cells

2014

Date of Acceptance: 29/05/2014 There is presently a lack of efficient and stable blue emitters for light-emitting electrochemical cells (LEECs), which limits the development of white light emitting systems for lighting. Cyclometalated iridium complexes as blue emitters tend to show low photoluminescence efficiency due to significant ligand-centred character of the radiative transition. The most common strategy to blue-shift the emission is to use fluorine substituents on the cyclometalating ligand, such as 2,4-difluorophenylpyridine, dFppy, which has been shown to decrease the stability of the emitter in operating devices. Herein we report a series of four new charged cyclometalated iridium…

PhotoluminescenceMaterials scienceLigandchemistry.chemical_elementGeneral ChemistryTime-dependent density functional theoryQD ChemistryPhotochemistryElectrochemistryElectrochemical cellchemistry.chemical_compoundchemistryPyridineMaterials ChemistryFluorineQDIridiumJ. Mater. Chem. C
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σ-Hammett parameter: a strategy to enhance both photo- and electro-luminescence features of heteroleptic copper(i) complexes

2017

This work studies the effect of the σ-Hammett parameter (σp) – i.e., the σ-donation effect caused by substitution at the para position of a bipyridine ligand (4,4′-R2bipy, where R is MeO, Me, H, NO2) – on both the photo- and electro-luminescence features of a series of heteroleptic copper(I) complexes – i.e., [Cu(N^N)(P^P)]+ where N^N and P^P ligands are R2bipy and Xantphos, respectively. By virtue of a comprehensive photophysical, theoretical, and thin-film lighting device – i.e., light-emitting electrochemical cells (LECs) – investigation, we note a clear relationship between the σp and the photo- and electro-luminescence parameters, such as photoluminescence quantum yields, excited-state…

PhotoluminescenceXantphosLigandchemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesCopper0104 chemical sciencesElectrochemical cellInorganic ChemistryPara positionchemistry.chemical_compoundBipyridinechemistryElectro luminescencePhysical chemistry0210 nano-technologyDalton Transactions
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Metallo-Polymer Chain Extension Controls the Morphology and Release Kinetics of Microparticles Composed of Terpyridine-Capped Polylactides and their …

2016

Control over morphology and porosity of supramolecular complexed polylactide (PLA) microparticles can be achieved by manipulation of the supramolecular interactions between their constituent polymeric building blocks. It is expected that such modular systems are ideal candidates to serve as degradable delivery carriers. In view of this goal, this study reports about a modular fabrication of biodegradable microparticles from terpyridine (TPy) and bisterpyridine (bisTPy) end-functionalized PLAs that can be transiently extended by chain association through differently strong complexation to three metal cations: Ni2+ , Co2+ , or Fe2+ . Further influence on the morphology of the particles can be…

Polymers and PlasticsPyridinesSurface PropertiesPolyestersKineticsSupramolecular chemistry02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundMaterials ChemistryOrganometallic CompoundsMicroparticleParticle SizePorositychemistry.chemical_classificationMolecular StructureChemistryOrganic ChemistryStereoisomerismPolymer021001 nanoscience & nanotechnologyControlled release0104 chemical sciencesKineticsChemical engineeringParticleTerpyridine0210 nano-technologyMacromolecular rapid communications
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Adduct formation by sub-coordinated metal complexes—VI. Synthesis and pyridine adducts of some nickel(II) chelates formally tri-coordinated

1976

Polymers and Plasticschemistry.chemical_elementAdductMetalchemistry.chemical_compoundNickelchemistryvisual_artPyridinePolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumOrganic chemistryChelationJournal of Inorganic and Nuclear Chemistry
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