Works matching DE "ACRIDINE derivatives"
Results: 168
Balanced Energy Gaps as a Key Design Rule for Solution‐Phase Organic Room Temperature Phosphorescence.
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- Chemistry - A European Journal, 2023, v. 29, n. 42, p. 1, doi. 10.1002/chem.202301369
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Structural Perspective into the Interaction of an Oncogenesis‐Relevant pre‐miRNA G‐Quadruplex Ligand Carrier with the Protein Nucleolin.
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- Chemistry - A European Journal, 2023, v. 29, n. 39, p. 1, doi. 10.1002/chem.202301181
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Programmable Photocatalytic Activity of Multicomponent Covalent Organic Frameworks Used as Metallaphotocatalysts.
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- Chemistry - A European Journal, 2023, v. 29, n. 4, p. 1, doi. 10.1002/chem.202202967
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Directing the Self‐Assembly of Aromatic Foldamer Helices using Acridine Appendages and Metal Coordination.
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- Chemistry - A European Journal, 2022, v. 28, n. 62, p. 1, doi. 10.1002/chem.202201345
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Orbital Engineering Mediated by Cation Conjugation in Luminescent Uranyl‐Organic Hybrid Materials.
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- Angewandte Chemie, 2024, v. 136, n. 7, p. 1, doi. 10.1002/ange.202318161
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Asymmetrically Substituted 10H,10′H‐9,9′‐Spirobi[acridine] Derivatives as Hole‐Transporting Materials for Perovskite Solar Cells.
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- Angewandte Chemie, 2022, v. 134, n. 48, p. 1, doi. 10.1002/ange.202212891
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Acridine‐Functionalized Covalent Organic Frameworks (COFs) as Photocatalysts for Metallaphotocatalytic C−N Cross‐Coupling.
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- Angewandte Chemie, 2022, v. 134, n. 21, p. 1, doi. 10.1002/ange.202117738
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Synthesis, Characterization and Biological Evaluations of New Imidazo[4,5-a]Acridines as Potential Antibacterial Agents.
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- Pharmaceutical Chemistry Journal, 2019, v. 53, n. 1, p. 52, doi. 10.1007/s11094-019-01955-8
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Transformation of Contaminants of Emerging Concern (CECs) during UV-Catalyzed Processes Assisted by Chlorine.
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- Catalysts (2073-4344), 2020, v. 10, n. 12, p. 1432, doi. 10.3390/catal10121432
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Palladium-Catalyzed Regioselective Alkoxylation via C-H Bond Activation in the Dihydrobenzo[c]acridine Series.
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- Catalysts (2073-4344), 2018, v. 8, n. 4, p. 139, doi. 10.3390/catal8040139
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Modelización molecular de las interacciones de 9-aminoacridinas con ácidos nucleicos.
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- Salud Uninorte, 2013, v. 29, n. 3, p. 351
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Ultrasound-Assisted One‐Pot Synthesis of 9-(Substituted heteroaryl) acridinedione Derivatives.
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- Duzce University Journal of Science & Technology, 2021, v. 9, n. 5, p. 1610, doi. 10.29130/dubited.926881
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Acridine derivatives as inhibitors/poisons of topoisomerase II.
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- Journal of Applied Toxicology, 2022, v. 42, n. 4, p. 544, doi. 10.1002/jat.4238
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New Imidazo[4,5-α] Acridine: Synthesis and Studying the Molecular Dynamics Simulation of Its Interaction with the Topoisomerase Enzyme.
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- Journal of Chemical Health Risks, 2024, v. 14, n. 1, p. 159, doi. 10.22034/jchr.2023.1984058.1724
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DESIGN, SYNTHESIS, AND IN VITRO EVALUATION OF NOVEL ACRIDINE DERIVATIVES AS MONOAMINE OXIDASE INHIBITORS.
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- Rasayan Journal of Chemistry, 2022, v. 15, n. 4, p. 2318, doi. 10.31788/RJC.2022.1547080
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EFFICIENT BIOLOGICAL ACTIVITY OF ACRIDINE SYNTHESISED BY MICROWAVE IRRADIATION WITH AN EFFICIENT NANOCATALYST.
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- Rasayan Journal of Chemistry, 2021, v. 14, n. 4, p. 2805, doi. 10.31788/RJC.2021.1446568
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Exploring tricycle acridines as prospective urease inhibitors: synthesis via microwave assistance, in vitro evaluation, kinetic profiling, and molecular docking investigations.
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- Journal of the Iranian Chemical Society, 2024, v. 21, n. 4, p. 1163, doi. 10.1007/s13738-024-02990-3
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Perspective on acridine: a versatile heterocyclic biologically imperative framework.
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- Journal of the Iranian Chemical Society, 2023, v. 20, n. 10, p. 2399, doi. 10.1007/s13738-023-02840-8
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Synthesis and antiproliferative activity of new hybrids bearing neocryptolepine, acridine and α-aminophosphonate scaffolds.
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- Journal of the Iranian Chemical Society, 2020, v. 17, n. 5, p. 1211, doi. 10.1007/s13738-019-01849-2
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Hollow FeO@DA-SOH: an efficient and reusable heterogeneous nano-magnetic acid catalyst for synthesis of dihydropyridine and dioxodecahydroacridine derivatives.
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- Journal of the Iranian Chemical Society, 2017, v. 14, n. 4, p. 791, doi. 10.1007/s13738-016-1029-1
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A green and efficient procedure for one-pot synthesis of xanthenes and acridines using silica boron-sulfuric acid nanoparticles (SBSANs) as a solid Lewis-protic acid.
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- Journal of the Iranian Chemical Society, 2013, v. 10, n. 2, p. 189, doi. 10.1007/s13738-012-0140-1
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Synthesis of Quinoline-2-Carboxylic Acid Aryl Ester and Its Apoptotic Action on PC3 Prostate Cancer Cell Line.
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- Applied Biochemistry & Biotechnology, 2023, v. 195, n. 8, p. 4818, doi. 10.1007/s12010-022-04258-z
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Suspect and non-target screening of chemicals in clothing textiles by reversed-phase liquid chromatography/hybrid quadrupole-Orbitrap mass spectrometry.
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- Analytical & Bioanalytical Chemistry, 2022, v. 414, n. 3, p. 1403, doi. 10.1007/s00216-021-03766-x
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Acridine as Bioinspired Corrosion Inhibitors.
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- Macromolecular Symposia, 2023, v. 407, n. 1, p. 1, doi. 10.1002/masy.202200106
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Full NMR assignment of new acridinyl‐chalcones, pyrazolino‐acridines, and spiro[imidazo[1,5‐b]pyrazole‐4,9′‐acridines].
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- Magnetic Resonance in Chemistry, 2020, v. 58, n. 8, p. 769, doi. 10.1002/mrc.5028
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<sup>1</sup>H, <sup>13</sup>C and <sup>15</sup>N NMR of spiro acridines integrated with pyrrole scaffolds.
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- Magnetic Resonance in Chemistry, 2020, v. 58, n. 2, p. 204, doi. 10.1002/mrc.4974
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Issue information - TOC.
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- Magnetic Resonance in Chemistry, 2016, v. 54, n. 1, p. 1, doi. 10.1002/mrc.4334
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Prediction by <sup>13</sup>C NMR of regioselectivity in 1,3-dipolar cycloadditions of acridin-9-yl dipolarophiles.
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- Magnetic Resonance in Chemistry, 2016, v. 54, n. 1, p. 8, doi. 10.1002/mrc.4307
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Strong deshielding in aromatic isoxazolines.
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- Magnetic Resonance in Chemistry, 2016, v. 54, n. 1, p. 17, doi. 10.1002/mrc.4308
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Detection of RNA Hydrolysis with Binase by Acridine Orange Fluorescence.
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- Applied Biochemistry & Microbiology, 2019, v. 55, n. 5, p. 518, doi. 10.1134/S0003683819050028
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Application of High-Performance Liquid Chromatography with Fluorescence Detection for Non-Polar Heterocyclic Aromatic Amines and Acridine Derivatives Determination in Pork Loin Roasted in a Roasting Bag.
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- Foods, 2022, v. 11, n. 21, p. 3385, doi. 10.3390/foods11213385
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Synthesis of 5‐Azatetracene and Comparison of Its Optical and Electrochemical Properties with Tetracene.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 10, p. 2571, doi. 10.1002/ajoc.202100373
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Redox/pH Dual Stimuli‐Responsive Acridine Spiropyran.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 6, p. 863, doi. 10.1002/ajoc.201900263
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Derivatives of 9-phosphorylated acridine as butyrylcholinesterase inhibitors with antioxidant activity and the ability to inhibit β-amyloid self-aggregation: potential therapeutic agents for Alzheimer's disease.
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- Frontiers in Pharmacology, 2023, p. 01, doi. 10.3389/fphar.2023.1219980
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Heterocyclic Schiff base derivatives containing pyrazolone moiety: Synthesis, characterization, and in vitro biological studies.
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- Journal of the Chinese Chemical Society, 2021, v. 68, n. 12, p. 2355, doi. 10.1002/jccs.202100357
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Copper/dapsone cuvalented Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub>‐propyl nanocomposite as a highly active and magnetically recoverable Lewis acid catalyst for the novel synthesis of bis‐dapsone derived acridines.
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- Journal of the Chinese Chemical Society, 2021, v. 68, n. 9, p. 1673, doi. 10.1002/jccs.202100095
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Monitoring Methionine Decarboxylase by a Supramolecular Tandem Assay.
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- Chemistry - An Asian Journal, 2022, v. 17, n. 10, p. 1, doi. 10.1002/asia.202200106
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Acridine N‐Heterocyclic Carbene Gold(I) Compounds: Tuning from Yellow to Blue Luminescence.
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- Chemistry - An Asian Journal, 2021, v. 16, n. 5, p. 521, doi. 10.1002/asia.202001380
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A Methodological Study on Tuning the Thermally Activated Delayed Fluorescent Performance by Molecular Constitution in Acridine–Benzophenone Derivatives.
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- Chemistry - An Asian Journal, 2018, v. 13, n. 9, p. 1187, doi. 10.1002/asia.201800173
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Effective Host Materials for Blue/White Organic Light-Emitting Diodes by Utilizing the Twisted Conjugation Structure in 10-Phenyl-9,10-Dihydroacridine Block.
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- Chemistry - An Asian Journal, 2015, v. 10, n. 6, p. 1402, doi. 10.1002/asia.201500235
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The Theoretical Description for a Sucralose Electrochemical Cathodical Determination over a 9-9'-Diacridyl-modified Electrode.
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- Orbital: The Electronic Journal of Chemistry, 2021, v. 13, n. 3, p. 219, doi. 10.17807/orbital.v13i3.1584
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Single Step Upgradation of Isatin to Bioactive Fused Heterocycles via Ring Expansion Reactions.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 4, p. 1, doi. 10.1002/ejoc.202301000
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Pd-catalyzed one-pot approach for installation of 9-aminoacridines via Buchwald-Hartwig amination and cycloaromatization.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 24, doi. 10.24820/ark.5550190.p011.823
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Molecular Engineering to Access Fluorescent Trackers of Organelles by Cyclization: Chemical Environment of Nitrogen Atom‐Modulated Targets.
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- Advanced Functional Materials, 2020, v. 30, n. 42, p. 1, doi. 10.1002/adfm.202004511
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Thermally Activated Delayed Fluorescence Conjugated Polymers with Backbone‐Donor/Pendant‐Acceptor Architecture for Nondoped OLEDs with High External Quantum Efficiency and Low Roll‐Off.
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- Advanced Functional Materials, 2018, v. 28, n. 10, p. 1, doi. 10.1002/adfm.201706916
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Lattice energetics and thermochemistry of acridine derivatives and substituted acridinium trifluoromethanesulphonates.
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- Journal of Thermal Analysis & Calorimetry, 2017, v. 129, n. 3, p. 1613, doi. 10.1007/s10973-017-6306-4
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Synthesis and Crystal Structure Analysis of Acridine Derivatives.
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- Crystallography Reports, 2021, v. 66, n. 6, p. 964, doi. 10.1134/S106377452106033X
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Antifungal Activity of Capridine β as a Consequence of Its Biotransformation into Metabolite Affecting Yeast Topoisomerase II Activity.
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- Pathogens, 2021, v. 10, n. 2, p. 189, doi. 10.3390/pathogens10020189
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Conjugates of Ultrasmall Quantum Dots and Acridine Derivatives as Prospective Nanoprobes for Intracellular Investigations.
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- Nanomaterials (2079-4991), 2021, v. 11, n. 9, p. 2160, doi. 10.3390/nano11092160
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Porous Organic Polymer with Free Carboxylic Acids (Carboxy‐POP) for Heterogeneous Catalytic One‐Pot Synthesis of Xanthenes and Acridines.
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- ChemCatChem, 2023, v. 15, n. 24, p. 1, doi. 10.1002/cctc.202300727
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