Works matching DE "ACRIDINE derivatives"
Results: 174
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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- Article
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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- Article
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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- Article
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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- Article
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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- Article
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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- Article
Thermochemiluminescence‐Based Sensitive Probes: Synthesis and Photophysical Characterization of Acridine‐Containing 1,2‐Dioxetanes Focusing on Fluorophore Push‐Pull Effects.
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- ChemPhotoChem, 2022, v. 6, n. 1, p. 1, doi. 10.1002/cptc.202100152
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- Article
A comparative study between acridine-based macrocycle chemosensor switches to Cd(II): synthesis, spectroscopy, and theoretical calculation.
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- Supramolecular Chemistry, 2021, v. 33, n. 6, p. 318, doi. 10.1080/10610278.2021.1999451
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- Article
Pyridine Derivatives of Acridine and Quinoline.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 12, p. 2230, doi. 10.1134/S1070363220120038
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- Article
Photocatalytic Systems Based on Acridine Salts Derivatives.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 7, p. 1229, doi. 10.1134/S1070363220070099
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Design of Novel Catalysts Based on Acridine Derivatives Immobilized on Carbon Materials for Molecular Hydrogen Production.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 5, p. 918, doi. 10.1134/S1070363219050104
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- Article
Synthesis and Antibacterial Activity of 9-Oxo-9,10-dihydroacridinecarboxylic Acids Esters Bearing a Triazole Fragment.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 4, p. 676, doi. 10.1134/S1070363218040102
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- Article
Synthesis of 9-aryl-3,4,6,7,9,10-hexahydroacridine-1,8(2 Н,5 Н)-diones.
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- 2017
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- Letter
Amino Derivatives of Acridine: Synthesis and Study of Anticholinesterase and Antioxidant Activity.
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- Doklady Chemistry, 2023, v. 509, n. 2, p. 100, doi. 10.1134/S0012500823700167
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- Article
Concurrent N- and C-Functionalization of Acridine with Ethyl Aryl-2-oxobut-3-ynoates in the Presence of Water: Synthesis of N-Alkenylacridin-9-ones.
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- Doklady Chemistry, 2022, v. 506, n. 1, p. 185, doi. 10.1134/S0012500822600365
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Reduction of Acridine and 9-Chloroacridine with Red Phosphorus in the KOH/DMSO System.
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- Doklady Chemistry, 2019, v. 487, n. 1, p. 177, doi. 10.1134/S001250081907005X
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- Article
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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- Article
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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- Article
Radiobiological and dosimetric assessment of DNA-intercalated 99mTc-complexes bearing acridine orange derivatives.
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- EJNMMI Research, 2020, v. 10, n. 1, p. 1, doi. 10.1186/s13550-020-00663-9
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- Article
Can Zeolite-Supporting Acridines Boost Their Anticancer Performance?
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- Journal of Functional Biomaterials, 2023, v. 14, n. 3, p. 173, doi. 10.3390/jfb14030173
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- Article
Preparation, characterization, and application of supported phosphate acid on the UiO-66-NH<sub>2</sub> as an efficient and bifunctional catalyst for the synthesis of acridines.
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- Research on Chemical Intermediates, 2023, v. 49, n. 4, p. 1545, doi. 10.1007/s11164-023-04969-w
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- Article
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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- Article
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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- Article
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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- Article
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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- Article
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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- Article
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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- Article
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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- Article
Acridine Orange Staining Technique - A Quick Diagnostic for Babesia gibsoni Infection.
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- Intas Polivet, 2018, v. 19, n. 2, p. 328
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- Article
Design and Synthesis of Acridine-Triazole and Acridine-Thiadiazole Derivatives and Their Inhibitory Effect against Cancer Cells.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 1, p. 64, doi. 10.3390/ijms24010064
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- Article
The Effect of Conjugation with Octaarginine, a Cell-Penetrating Peptide on Antifungal Activity of Imidazoacridinone Derivative.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 24, p. 13190, doi. 10.3390/ijms222413190
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- Article
Silver (I) N -Heterocyclic Carbene Complexes: A Winning and Broad Spectrum of Antimicrobial Properties.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 5, p. 2497, doi. 10.3390/ijms22052497
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- Article
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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- Article
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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- Article
Synthesis of N-Arylquinone Diimine Derivatives of 2H-Benzimidazo[2,1-e]acridine and Their Reactions with Aromatic Amines.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 2, p. 152, doi. 10.1134/S1070428019020052
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- Article
3 H-Benzo[ a]imidazo[4,5- j]acridine as a new fluorescent heterocyclic system: synthesis, spectral studies, and quantum chemical investigation.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 10, p. 1586, doi. 10.1134/S1070428017100165
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- Article
Synthesis of 8,16-diarylacridino[4,3- c]acridine-1,9-dione derivatives.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 3, p. 383, doi. 10.1134/S1070428016030155
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- Article
Retraction Note to: Acridine yellow. A novel use to estimate and measure the plasma membrane potential in Saccharomyces cerevisiae.
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- Journal of Bioenergetics & Biomembranes, 2019, v. 51, n. 4, p. 313, doi. 10.1007/s10863-019-09801-y
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- Article
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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- Article
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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- Article
Ultrasound-assisted synthesis of 1, 8-dioxodecahydroacridine derivatives in presence of Ag doped CdS nanocatalyst.
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- Journal of Dispersion Science & Technology, 2020, v. 41, n. 8, p. 1145, doi. 10.1080/01932691.2019.1614460
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- Article
Cholinesterases inhibitors for treating Alzheimer's disease.
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- International Journal of Pharmaceutical Research (09752366), 2020, v. 12, n. 4, p. 713, doi. 10.31838/ijpr/2020.12.04.114
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- Article
An Efficient Synthesis of Fused Polycyclic Triazolo[4,5- a ]acridine Derivatives under Catalyst-Free Conditions with High Regioselectivity.
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- Polycyclic Aromatic Compounds, 2016, v. 36, n. 5, p. 671, doi. 10.1080/10406638.2015.1042553
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- Article
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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- Article
Screening of Scaffolds for the Design of G-Quadruplex Ligands.
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- Applied Sciences (2076-3417), 2022, v. 12, n. 4, p. 2170, doi. 10.3390/app12042170
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- Article
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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- Article
A 9-aminoacridine derivative induces growth inhibition of Ehrlich ascites carcinoma cells and antinociceptive effect in mice.
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- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.963736
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- Article
Catalytic condensation for the formation of polycyclic heteroaromatic compounds.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04143-6
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- Article
Effect of Acridine Orange on Pathogenicity of E. coli Isolated from Urinary Tract Infection Patients.
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- Indian Journal of Forensic Medicine & Toxicology, 2020, v. 14, n. 4, p. 4116, doi. 10.37506/ijfmt.v14i4.12286
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- Article
Core‐Shell Nano‐Cobalt Catalyzed Chemoselective Reduction of N‐Heteroarenes with Ammonia Borane.
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- ChemSusChem, 2022, v. 15, n. 23, p. 1, doi. 10.1002/cssc.202201522
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- Article