Works matching DE "ACRIDINE"
Results: 401
Structure Engineering of Acridine Donor to Optimize Color Purity of Blue Thermally Activated Delayed Fluorescence Emitters.
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- Chemistry - A European Journal, 2024, v. 30, n. 37, p. 1, doi. 10.1002/chem.202401250
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- Article
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
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
Identification of novel inhibitors for Pim-1 kinase using pharmacophore modeling based on a novel method for selecting pharmacophore generation subsets.
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- Journal of Computer-Aided Molecular Design, 2016, v. 30, n. 1, p. 39, doi. 10.1007/s10822-015-9887-7
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- Article
Determination of an adequate perfusion pressure for continuous dual vessel hypothermic machine perfusion of the rat liver.
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- Transplant International, 2007, v. 20, n. 4, p. 343, doi. 10.1111/j.1432-2277.2006.00433.x
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- Article
Structure of the AcrAB-TolC multidrug efflux pump.
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- Nature, 2014, v. 509, n. 7501, p. 512, doi. 10.1038/nature13205
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- Article
Features of Behavior of Acridinium Salt in the Production of Emulsion Rubbers.
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- Theoretical Foundations of Chemical Engineering, 2024, v. 58, n. 1, p. 60, doi. 10.1134/S0040579524700131
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- Article
Characterization of DNA-loaded porous polyethersulfone particles prepared by phase inversion technique.
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- Colloid Journal, 2005, v. 67, n. 2, p. 140, doi. 10.1007/s10595-005-0073-9
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- Article
Adsorption of the Dyes (Methylene Blue and Acridine Orange and Their Mixtures) from Aqueous Solutions on Cholesterol Surface.
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- Colloid Journal, 2003, v. 65, n. 3, p. 350, doi. 10.1023/A:1024215008489
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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
The ethanol extraction of prepared Psoralea corylifolia induces apoptosis and autophagy and alteres genes expression assayed by cDNA microarray in human prostate cancer PC‐3 cells.
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- Environmental Toxicology, 2018, v. 33, n. 7, p. 770, doi. 10.1002/tox.22564
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- Article
Effects of N-Heterocyclic Polyaromatic Hydrocarbons on Survival, Reproduction, and Biochemical Parameters in Daphnia magna.
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- Environmental Toxicology, 2006, v. 21, n. 4, p. 425, doi. 10.1002/tox.20198
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- Article
A comparison of two different fluorochrome stains for the detection of acid-fast bacilli in sputum specimens.
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- Turkish Journal of Medical Sciences, 2011, v. 41, n. 3, p. 411, doi. 10.3906/sag-1005-797
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- Article
Unique spectral signatures of the nucleic acid dye acridine orange can distinguish cell death by apoptosis and necroptosis.
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- Journal of Cell Biology, 2017, v. 216, n. 4, p. 1163, doi. 10.1083/jcb.201602028
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- Article
Zn /Cd optical discrimination by fluorescent acridine-based bis -macrocylic receptors.
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- Supramolecular Chemistry, 2017, v. 29, n. 11, p. 912, doi. 10.1080/10610278.2017.1387262
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- Article
A convenient and efficient one-pot method for the synthesis of novel acridine-calix[4]arene derivatives as new DNA binding agents via multicomponent reaction.
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- Supramolecular Chemistry, 2014, v. 26, n. 5/6, p. 442, doi. 10.1080/10610278.2013.832763
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- Article
The Host-Guest Chemistry of Proflavine with Cucurbit[6,7,8]urils.
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- Supramolecular Chemistry, 2007, v. 19, n. 7, p. 475, doi. 10.1080/10610270601124019
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- Article
A Comparative Study of Complexation of β-Cyclodextrin, Calix[4]arenesulfonate and Cucurbit[7]uril with Dye Guests: Fluorescence Behavior and Binding Ability.
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- Supramolecular Chemistry, 2007, v. 19, n. 7, p. 517, doi. 10.1080/10610270601145444
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- Article
Strapped-calix[4]pyrroles Bearing Acridine Moiety.
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- Supramolecular Chemistry, 2007, v. 19, n. 4/5, p. 271, doi. 10.1080/10610270701358517
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- Article
Effects of Bis(aromatic) Pendants on Recognition of Nucleobase Thymine by Zn -1,4,7,10-tetraazacyclododecane (Zn -cyclen).
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- Supramolecular Chemistry, 2002, v. 14, n. 2/3, p. 95, doi. 10.1080/10610270290025997
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- Article
Photochemical Production of Molecular Hydrogen in the Presence of Substituted Acridine Salts.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 12, p. 2816, doi. 10.1134/S1070363222120325
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- Article
Unexpected Reaction of Secondary Phosphine Chalcogenides with Acridine.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 3, p. 543, doi. 10.1134/S1070363219030290
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- Article
Synthesis and Antibacterial Activity of New N<sup>9</sup>-Substituted Acridine-9-amines.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 1, p. 157, doi. 10.1134/S1070363219010298
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- Article
Nucleophilic substitution of chlorine in 9-chloroacridine with amino(hydrazine, thioxo)-1,2,4-triazines.
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- 2016
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- Letter
Azinyl derivatives of ferrocene for preparation of poly(methyl methacrylate) with enhanced properties.
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- 2014
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- Letter
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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- Article
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
Investigating the Effects of Organonitrogen Types on Hydrodearomatization Reactions over Commercial NiMoS Catalyst.
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- Catalysts (2073-4344), 2022, v. 12, n. 7, p. N.PAG, doi. 10.3390/catal12070736
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- Article
Chemotherapeutic potential of 9-phenyl acridine: biophysical studies on its binding to DNA.
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- European Biophysics Journal, 2010, v. 39, n. 8, p. 1243, doi. 10.1007/s00249-010-0577-z
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- Article
Acridine derivatives inhibit lysozyme aggregation.
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- European Biophysics Journal, 2008, v. 37, n. 7, p. 1261, doi. 10.1007/s00249-008-0313-0
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- Article
Tunably strained metallacycles enable modular differentiation of aza-arene C–H bonds.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39753-2
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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
SYNTHESIS, CHARACTERISATION AND ANTIMICROBIAL EVALUATIONS OF ACETYLOXYPHENYL-1,2,3-TRIAZOLOTETRAMETHYL HEXAHYDROACRIDINEDIONES.
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- Rasayan Journal of Chemistry, 2022, v. 15, n. 2, p. 946, doi. 10.31788/RJC.2022.1526718
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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
Cocrystal Assembled by 1,2-Diiodotetrafluorobenzene and Acridine via CI···N Halogen Bond and π-hole···F Bonds.
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- Chinese Journal of Chemistry, 2013, v. 31, n. 10, p. 1279, doi. 10.1002/cjoc.201300692
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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
Immobilization of organofunctionalized silica (SiMPTMS) with biphenyl-2,2′-dioic acid and investigation of its catalytic property for one-pot tandem synthesis of acridine-1,8-dione derivatives.
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- Journal of the Iranian Chemical Society, 2017, v. 14, n. 10, p. 2199, doi. 10.1007/s13738-017-1156-3
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- Article
Synthesis of novel 1,8-dioxo octahydroacridine functionalized thioureas and thiazolidinones and evaluation of their antimicrobial activities.
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- Journal of the Iranian Chemical Society, 2017, v. 14, n. 3, p. 727, doi. 10.1007/s13738-016-1024-6
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- Article
Novel Imidazolyi Derivatives of 1,8-Acridinedione as Potential DNA-Intercalating Agents.
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- Journal of the Iranian Chemical Society, 2011, v. 8, n. 4, p. 1098, doi. 10.1007/BF03246568
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- Article
Synthesis, Cytotoxicity and Calcium Antagonist Activity of Novel Imidazolyl Derivatives of 1,8-Acridinediones.
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- Journal of the Iranian Chemical Society, 2011, v. 8, n. 4, p. 983, doi. 10.1007/BF03246554
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- Article
Two Zn(II) and Cd(II) Compounds Derived from 9-Aminoacridine: Syntheses, Characterizations, Crystal Structures and Solution Studies.
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- Journal of the Iranian Chemical Society, 2011, v. 8, n. 3, p. 734, doi. 10.1007/BF03245905
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One-Pot Facile Synthesis of Acridine Derivatives under Solvent-Free Condition.
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- Journal of the Iranian Chemical Society, 2010, v. 7, n. 4, p. 957, doi. 10.1007/BF03246091
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- Article
Effects of cryopreservation on plasma membrane glycoconjugates of human spermatozoa.
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- Iranian Journal of Reproductive Medicine, 2010, v. 8, n. 3, p. 119
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- Article
BIOTRANSFORMATION OF ACRIDINE BY MYCOBACTERIUM VANBAALENII.
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- Environmental Toxicology & Chemistry, 2009, v. 28, n. 1, p. 61, doi. 10.1897/08-206.1
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- Article
Effects and uptake of polycyclic aromatic compounds in snails (Helix aspersa).
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- Environmental Toxicology & Chemistry, 2006, v. 25, n. 7, p. 1941, doi. 10.1897/05-620R1.1
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- Article
CYTOTOXICITY AND ARYL HYDROCARBON RECEPTOR--MEDIATED ACTIVITY OF N-HETEROCYCLIC POLYCYCLIC AROMATIC HYDROCARBONS: STRUCTURE-ACTIVITY RELATIONSHIPS.
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- Environmental Toxicology & Chemistry, 2006, v. 25, n. 5, p. 1291, doi. 10.1897/05-388R.1
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- Article
ESTIMATION OF KINETIC PARAMETER FOR THE BIOTRANSFORMATION OF THREE-RING AZAARENES BY THE PHENANTHRENE-DEGRADING STRAIN SPHINGOMONAS SP. LH128.
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- Environmental Toxicology & Chemistry, 2004, v. 23, n. 2, p. 331, doi. 10.1897/03-147
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- Article
THE ROLE OF ULTRAVIOLET-ADAPTATION OF A MARINE DIATOM IN PHOTOENHANCED TOXICITY OF ACRIDINE.
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- Environmental Toxicology & Chemistry, 2003, v. 22, n. 3, p. 591, doi. 10.1002/etc.5620220318
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- Article
EFFECTS OF EIGHT POLYCYCLIC AROMATIC COMPOUNDS ON THE SURVIVAL AND REPRODUCTION OF THE SPRINGTAIL FOLSOMIA FIMETARIA L. (COLLEMBOLA, ISOTOMIDAE).
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- Environmental Toxicology & Chemistry, 2001, v. 20, n. 6, p. 1332, doi. 10.1897/1551-5028(2001)020<1332:EOEPAC>2.0.CO;2
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- Article
Photodynamic therapy of multidrug resistant leukemic murine cells by 3,6-bis(alkylthiourea)acridine hydrochlorides.
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- Neoplasma, 2021, v. 68, n. 6, p. 1169, doi. 10.4149/neo_2021_210324N390
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- Article