Works matching Phenothiazine
Results: 1860
Heterocyclization of N-propenyl-substituted phenothiazines and phenoxazines using electrophiles in an anhydrous medium.
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- Chemistry of Heterocyclic Compounds, 2008, v. 44, n. 12, p. 1505, doi. 10.1007/s10593-009-0219-5
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Antioxidant Properties of New Phenothiazine Derivatives.
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- Antioxidants, 2022, v. 11, n. 7, p. 1371, doi. 10.3390/antiox11071371
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Phenothiazines suppress proliferation and induce apoptosis in cultured leukemic cells without any influence on the viability of normal lymphocytes: Phenothiazines and leukemia.
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- Cancer Chemotherapy & Pharmacology, 2004, v. 53, n. 3, p. 267, doi. 10.1007/s00280-003-0738-1
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Electrochemical C–H/N–H Coupling of Phenothiazines with Halogenated Phenols.
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- Russian Journal of General Chemistry, 2024, v. 94, n. 11, p. 3104, doi. 10.1134/S1070363224110343
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Synthesis and characterization of thermally stable polyimides with a pendent phenothiazine unit based on new diamine 10-(3,5-diaminobenzoyl)phenothiazine.
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- High Performance Polymers, 2016, v. 28, n. 1, p. 26, doi. 10.1177/0954008314568877
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Exploring the Theoretical Foundations of Thermally Activated Delayed Fluorescence (TADF) Emission: A Comprehensive TD‐DFT Study on Phenothiazine Systems.
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- Chemistry - A European Journal, 2024, v. 30, n. 20, p. 1, doi. 10.1002/chem.202304206
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Sequential C−F Bond Transformation of the Difluoromethylene Unit in Perfluoroalkyl Groups: A Combination of Fine‐Tuned Phenothiazine Photoredox Catalyst and Lewis Acid.
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- Angewandte Chemie, 2024, v. 136, n. 14, p. 1, doi. 10.1002/ange.202401117
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The Effect of Molecular Conformations and Simulated "Self‐Doping" in Phenothiazine Derivatives on Room‐Temperature Phosphorescence.
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- Angewandte Chemie, 2023, v. 135, n. 5, p. 1, doi. 10.1002/ange.202214908
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Development of High Energy Density Diaminocyclopropenium‐Phenothiazine Hybrid Catholytes for Non‐Aqueous Redox Flow Batteries.
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- Angewandte Chemie, 2021, v. 133, n. 52, p. 27245, doi. 10.1002/ange.202111939
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Luminescent Behavior Elucidation of a Disilane‐Bridged D–A–D Triad Composed of Phenothiazine and Thienopyrazine.
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- Angewandte Chemie, 2021, v. 133, n. 42, p. 23053, doi. 10.1002/ange.202108089
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Strong Ground‐ and Excited‐State Charge Transfer in C<sub>3</sub>‐Symmetric Truxene‐Derived Phenothiazine‐Tetracyanobutadine and Expanded Conjugates.
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- Angewandte Chemie, 2019, v. 131, n. 13, p. 4394, doi. 10.1002/ange.201814388
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Spectroelectrochemical Properties of 1,10‐Phenanthroline Substituted by Phenothiazine and Carbazole Redox‐active Units.
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- ChemElectroChem, 2021, v. 8, n. 15, p. 2935, doi. 10.1002/celc.202100835
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Inhibition of Butyrylcholinesterase by Phenothiazine Derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2002, v. 17, n. 3, p. 197, doi. 10.1080/1475636021000003165
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Inhibition of Bacterial RNase P RNA by Phenothiazine Derivatives.
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- Biomolecules (2218-273X), 2016, v. 6, n. 3, p. 38, doi. 10.3390/biom6030038
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Discovery of novel phenothiazine derivatives as new agrochemical alternatives for treating plant viral diseases.
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- Pest Management Science, 2023, v. 79, n. 11, p. 4231, doi. 10.1002/ps.7623
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The role of phenothiazine derivatives in autophagy regulation: A systematic review.
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- Journal of Applied Toxicology, 2023, v. 43, n. 4, p. 474, doi. 10.1002/jat.4397
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Synthesis and Characterization of Novel Ionochromic Tricyanofuran-Based Phenothiazine Fluorophore: Cellulose-Based Xerogel for Colorimetric Detection of Toxic Cyanides.
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- Journal of Polymers & the Environment, 2022, v. 30, n. 7, p. 3107, doi. 10.1007/s10924-022-02418-0
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The effect of treatment with risperidone, olanzapine or phenothiazines on cognitive functions in patients with schizophrenia.
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- International Journal of Psychiatry in Clinical Practice, 2001, v. 5, n. 4, p. 249, doi. 10.1080/13651500152732595
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Synergy between Phenothiazines and Oxacillin against Clinical Isolates of Methicillin-Resistant Staphylococcus aureus.
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- Tropical Journal of Pharmaceutical Research, 2010, v. 9, n. 3, p. 243, doi. 10.4314/tjpr.v9i3.56284
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Phenothiazine-induced systemic lupus erythematosus: a case report.
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- European Psychiatry, 2020, v. 63, p. S491
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Reversible Fluorescence Modulation in a Dyad Comprising Phenothiazine Derivative and Spiropyran.
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- Asian Journal of Organic Chemistry, 2018, v. 7, n. 11, p. 2254, doi. 10.1002/ajoc.201800338
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Effect of Spacer Connecting the Secondary Electron Donor Phenothiazine in Subphthalocyanine-Fullerene Conjugates in Promoting Electron Transfer Followed by Hole Shift Process.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 8, p. 1246, doi. 10.1002/asia.201501372
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π‐Conjugation Enables Ultra‐High Rate Capabilities and Cycling Stabilities in Phenothiazine Copolymers as Cathode‐Active Battery Materials.
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- Advanced Functional Materials, 2019, v. 29, n. 45, p. N.PAG, doi. 10.1002/adfm.201906436
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Analysis of Some Phenothiazine Drugs and Their S-Oxides using Enzymatic Method of Cholinesterase Inhibition.
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- Methods & Objects of Chemical Analysis / Metody & Obekty Himičeskogo Analiza, 2023, v. 18, n. 3, p. 143, doi. 10.17721/moca.2023.143-151
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Analytical Application of the Binary and Ternary Complexes of 2,10-Disubstituted Phenothiazines.
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- Analytical Letters, 2008, v. 41, n. 16, p. 2893, doi. 10.1080/00032710802440558
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Determination of Some Phenothiazines Compounds in Pharmaceuticals and Human Body Fluid by Electrocatalytic Oxidation at a Glassy Carbon Electrode Using Methylene Blue as a Mediator.
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- Analytical Letters, 2008, v. 41, n. 13, p. 2487, doi. 10.1080/00032710802352555
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Determination of Five Phenothiazines in Pure and Pharmaceutical Preparations Using Vanadium Pentoxide as a Chromogenic Reagent.
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- Analytical Letters, 2003, v. 36, n. 14, p. 2961, doi. 10.1081/AL-120026414
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Development of Turbidimetric Methods for the Determination of Some N-Substituted Phenothiazine Derivatives Using Sodium Dodecyl Sulfate and Mercury(II) Chloride.
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- Analytical Letters, 2003, v. 36, n. 10, p. 2183, doi. 10.1081/AL-120023710
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Phenothiazine Drugs as Redox Mediators in Horseradish Peroxidase Bioelectrocatalysis.
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- Analytical Letters, 2003, v. 36, n. 9, p. 1819, doi. 10.1081/AL-120023616
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Recent Developments of Antipsychotic Drugs with Phenothiazine Hybrids: A Review.
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- Chemistry & Biology Interface, 2022, v. 12, n. 4, p. 77
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The anti-cancer efficacy of a novel phenothiazine derivative is independent of dopamine and serotonin receptor inhibition.
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- Frontiers in Oncology, 2023, p. 1, doi. 10.3389/fonc.2023.1295185
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Electro-oxidative polymerization of phenothiazine dyes into a multilayer-containing carbon nanotube on a glassy carbon electrode for the sensitive and low-potential detection of NADH.
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- Microchimica Acta, 2010, v. 168, n. 3/4, p. 299, doi. 10.1007/s00604-009-0283-7
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Adsorption process of phenothiazine solution in dimethyl sulfoxide on graphite electrodes.
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- Journal of Solid State Electrochemistry, 2018, v. 22, n. 8, p. 2305, doi. 10.1007/s10008-018-3930-2
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Novel copper-catalyzed rearrangement of 2-aminobenzothiazoles to phenothiazines.
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- Chemistry of Heterocyclic Compounds, 2012, v. 48, n. 9, p. 1420, doi. 10.1007/s10593-012-1154-4
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Comparative Study of Quasi-Solid-State Dye-Sensitized Solar Cells Using Z907, N719, Photoactive Phenothiazine Dyes and PVDF-HFP Gel Polymer Electrolytes with Different Molecular Weights.
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- Photonics, 2024, v. 11, n. 8, p. 760, doi. 10.3390/photonics11080760
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Phenothiazine-Based D-A-π-A Dyes for Highly Efficient Dye-Sensitized Solar Cells: Effect of Internal Acceptor and Non-Conjugated π-Spacer on Device Performance.
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- ChemPlusChem, 2017, v. 82, n. 2, p. 280, doi. 10.1002/cplu.201600492
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DSSCs Sensitized with Phenothiazine Derivatives Containing 1H-Tetrazole-5-acrylic Acid as an Anchoring Unit.
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- Materials (1996-1944), 2024, v. 17, n. 24, p. 6116, doi. 10.3390/ma17246116
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Continuous‐Flow Synthesis of Phenothiazine Antipsychotics: A Feasibility Study.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 6, p. 1350, doi. 10.1002/ejoc.201801689
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The Relative Efficacy of Phenothiazines for the Treatment of Acute Migraine: A Meta-Analysis.
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- Headache: The Journal of Head & Face Pain, 2009, v. 49, n. 9, p. 1324, doi. 10.1111/j.1526-4610.2009.01465.x
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Review: Phenothiazines relieve acute migraine headaches in the ED and are better than other active agents for some outcomes.
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- ACP Journal Club, 2010, v. 152, n. 4, p. 10
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Synthesis and evaluation of antimicrobial and anthelmintic activity of novel fluorinated 7-ethyl-10 H-phenothiazines, their sulphones and ribofuranosides.
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- Journal of Chemical Sciences, 2014, v. 126, n. 1, p. 197, doi. 10.1007/s12039-013-0551-2
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Synthesis and pharmaceutical importance of 2-azetidinone derivatives of phenothiazine.
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- Journal of Chemical Sciences, 2012, v. 124, n. 3, p. 633, doi. 10.1007/s12039-012-0257-x
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Cross-Coupling of Phenothiazines with Phenols: Para-Selective Molecular Oxygen-assisted C(sp<sup>2</sup>)H/NH Cross-Coupling.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 11, p. 2765, doi. 10.1002/bkcs.10536
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Synthesis and Characterization of Phenothiazine-Isoindigo Copolymers for Photovoltaic Applications.
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- Bulletin of the Korean Chemical Society, 2014, v. 35, n. 6, p. 1875, doi. 10.5012/bkcs.2014.35.6.1875
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Dissolution Thermodynamics and Preferential Solvation of Phenothiazine in Some Aqueous Cosolvent Systems.
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- Liquids (2673-8015), 2024, v. 4, n. 2, p. 443, doi. 10.3390/liquids4020024
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Phenothiazine Radicals Inactivate Trypanosoma cruzi Dihydrolipoamide Dehydrogenase: Enzyme Protection by Radical Scavengers.
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- Free Radical Research, 2003, v. 37, n. 3, p. 281
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Exploring Micelles and Nanospheres as Delivery Systems for Phenothiazine Derivatives in Cancer Therapy.
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- Pharmaceutics, 2024, v. 16, n. 12, p. 1597, doi. 10.3390/pharmaceutics16121597
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Molecular Modelling, Hirshfeld Surface Analysis, Molecular Docking and Therapeutic Potential of Phenothiazine Derived Quinizarin.
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- Current Trends in Biotechnology & Pharmacy, 2025, v. 19, n. 1, p. 2144, doi. 10.5530/ctbp.2025.1.4
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EVALUATION OF PHENOTHIAZINE AS ENVIRONMENTALLY FRIENDLY CORROSION INHIBITOR FOR BRONZE IN SYNTHETIC ACID RAIN.
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- Studia Universitatis Babes-Bolyai, Chemia, 2013, v. 58, n. 3, p. 53
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SYNTHESIS, CHARACTERIZATION AND COMPLEXATION STUDY OF NEW 4-(DIPHENYLPHOSPHINO)-PHENOTHIAZINES.
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- Studia Universitatis Babes-Bolyai, Chemia, 2011, v. 56, n. 4, p. 191
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