Works matching DE "THIADIAZOLES"
Results: 1110
Salicylic Acid and a Chitin Elicitor Both Control Expression of the CAD1 Gene Involved in the Plant Immunity of Arabidopsis.
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- Bioscience, Biotechnology & Biochemistry, 2006, v. 70, n. 9, p. 2042, doi. 10.1271/bbb.50700
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Theoretical study on photophysical properties of 2,1,3-benzothiadiazole-based star-shaped molecules.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2011, v. 129, n. 6, p. 833, doi. 10.1007/s00214-011-0942-8
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Tuning the electronic structures and optical properties of fluorene-based donor-acceptor copolymers by changing the acceptors: a theoretical study.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2011, v. 129, n. 2, p. 257, doi. 10.1007/s00214-011-0932-x
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Synthesis of Novel Disubstituted Pyrazolo[1,5- a]pyrimidines, Imidazo[1,2- a]pyrimidines, and Pyrimido[1,2- a]benzimidazoles Containing Thioether and Aryl Moieties.
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- Helvetica Chimica Acta, 2012, v. 95, n. 6, p. 989, doi. 10.1002/hlca.201100495
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Synthesis, antimicrobial and antioxidant activities of 5-((2-oxo-2 H-chromen-7-yloxy)methyl)-1,3,4-thiadiazol-2(3 H)-one derived from umbelliferone.
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- Chemistry of Natural Compounds, 2013, v. 48, n. 6, p. 950, doi. 10.1007/s10600-013-0436-0
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Crystalsolvates of N-(3-ethylthio-1,2,4-thiadiazol-5-yl-aminocarbonylmethyl)cytisine.
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- Chemistry of Natural Compounds, 2008, v. 44, n. 4, p. 466, doi. 10.1007/s10600-008-9098-8
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1,2,4-Thiadiazole derivatives of cytisine.
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- Chemistry of Natural Compounds, 2004, v. 40, n. 6, p. 582, doi. 10.1007/s10600-005-0042-x
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3-Spiroandrostene-substituted 1,3,4-thiadiazolines.
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- Chemistry of Heterocyclic Compounds, 2024, v. 60, n. 3/4, p. 190, doi. 10.1007/s10593-024-03317-z
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A method for the synthesis of spiro-1,3,4-thiadiazolines.
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- Chemistry of Heterocyclic Compounds, 2024, v. 60, n. 3/4, p. 183, doi. 10.1007/s10593-024-03316-0
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Discovery of indole-3-acetic acid derivatives containing 1,3,4-thiadiazole thioether and amide moieties as novel antibacterial agents.
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- Chemistry of Heterocyclic Compounds, 2024, v. 60, n. 1/2, p. 92, doi. 10.1007/s10593-024-03298-z
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The effect of electron-donating moiety structure on the electrochemical and photophysical properties of dithiophene- and naphtho[2,1-b:3,4-b']dithiophene-substituted 1,3,4-oxadiazoles and 1,3,4-thiadiazoles.
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- Chemistry of Heterocyclic Compounds, 2023, v. 59, n. 1/2, p. 88, doi. 10.1007/s10593-023-03166-2
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Benzobischalcogenadiazoles: synthesis and applications (microreview).
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- Chemistry of Heterocyclic Compounds, 2022, v. 58, n. 6/7, p. 307, doi. 10.1007/s10593-022-03088-5
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Synthesis of 5-azolyl-2,4-dihydro-3H-1,2,4-triazole-3-thiones and 5-azolyl-1,3,4-thiadiazol-2-amines based on derivatives of 5-arylisoxazole-3-carboxylic and 4,5-dichloroisothiazole-3-carboxylic acids.
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- Chemistry of Heterocyclic Compounds, 2021, v. 57, n. 5, p. 594, doi. 10.1007/s10593-021-02948-w
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Preparation of 1,3,4-oxadiazoles and 1,3,4-thiadiazoles via chemoselective сyclocondensation of electrophilically activated nitroalkanes to (thio)semicarbazides or thiohydrazides.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 8, p. 1067, doi. 10.1007/s10593-020-02775-5
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Synthesis and Evaluation of Biological Activity of Homodrimane Sesquiterpenoids Bearing 1,3,4-Oxadiazole or 1,3,4-Thiadiazole Units.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 5, p. 578, doi. 10.1007/s10593-020-02703-7
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Sodium hypochlorite-mediated synthesis of 2,5-disubstituted 1,3,4-oxadiazoles from hydrazides and aldehydes.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 3, p. 371, doi. 10.1007/s10593-020-02669-6
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Synthesis of novel (2,3-dihydro-1,4-thiaselenin-2-yl)sulfanyl-substituted pharmacophoric nitrogen heterocycles based on 2-(bromomethyl)-1,3-thiaselenole.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 2, p. 226, doi. 10.1007/s10593-020-02648-x
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Synthesis, Optical and Electrochemical Properties of D1–A–D2–A–D1 Type Conjugated Donor-Acceptor Assemblies of Five-Membered Aromatic Heterocycles.
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- Chemistry of Heterocyclic Compounds, 2019, v. 55, n. 12, p. 1262, doi. 10.1007/s10593-019-02610-6
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Synthesis of 5-(5-amino-1H-pyrazol-1-yl)-1,2,3-thiadiazole-4-carboxylic acid ethyl esters and their cyclization into pyrazolo[1,5-a][1,2,3]thiadiazolo[4,5-e]pyrimidin-4(5H)-ones.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 11, p. 1079, doi. 10.1007/s10593-018-2396-6
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Interaction of condensed tetrahydropyrido[4,3-<italic>d</italic>]pyrimidin-4-ones with dehydrobenzene - synthesis of 6-vinylpyrimidinones fused with five-membered heterocycle containing two or three heteroatoms.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 2, p. 173, doi. 10.1007/s10593-018-2250-x
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Synthesis of 2-polyfluoroalkyl-2,3-dihydro-1,3,4-thiadiazoles via regioselective [3+2] cycloaddition of nitrile imines to polyfluoroalkanethioamides.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 11, p. 1268, doi. 10.1007/s10593-018-2199-9
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Synthesis of 5-(pyrazol-1-yl)-1,2,3-thiadiazoles.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 2, p. 236, doi. 10.1007/s10593-017-2045-5
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Synthesis of Assemblies of Isoxazole and Azoles Based on 1,3-Dipolar Cycloaddition Reaction of Enamines with Nitrile Oxides.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 9, p. 743, doi. 10.1007/s10593-016-1958-8
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Synthesis of N-heteroarylamidines of 1,2,3-thiadiazole-4-carboxylic acid from 2-cyanothioacetamides and 5-azido-1-methyl-4-nitroimidazole.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 3, p. 206, doi. 10.1007/s10593-016-1861-3
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Synthesis and anticancer activity of arylazothiazoles and 1,3,4-thiadiazoles using chitosan-grafted-poly(4-vinylpyridine) as a novel copolymer basic catalyst.
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- Chemistry of Heterocyclic Compounds, 2015, v. 51, n. 11/12, p. 1030, doi. 10.1007/s10593-016-1815-9
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Halocyclization of S- and N-alkenyl derivatives of 5-methyl-1,3,4-thiadiazole-2-thione.
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- Chemistry of Heterocyclic Compounds, 2015, v. 51, n. 10, p. 923, doi. 10.1007/s10593-015-1797-z
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Synthesis and Study of α-Glucosidase Inhibitory, Antimicrobial and Antioxidant Activities of Some Benzimidazole Derivatives Containing Triazole, Thiadiazole, Oxadiazole, and Morpholine Rings.
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- Chemistry of Heterocyclic Compounds, 2015, v. 50, n. 12, p. 1671, doi. 10.1007/s10593-015-1637-1
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Сonvenient Access to 1,3-Dimethyl[1,2,4]Triazolo[3,4- b][1,3,4]-Thiadiazol-1-Ium and 7 H-[1,2,4]Triazolo[4,3- b][1,2,4]Triazol-1-Ium Salts.
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- Chemistry of Heterocyclic Compounds, 2015, v. 51, n. 2, p. 159, doi. 10.1007/s10593-015-1674-9
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Reaction of 3-Aryl-2-Cyanoprop-2-ene- Thioamides With Bromonitromethane: A new Method for the Synthesis of Functionalized 1,2,4-Thiadiazoles.
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- Chemistry of Heterocyclic Compounds, 2014, v. 50, n. 4, p. 557, doi. 10.1007/s10593-014-1507-2
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One-pot, Three-component Synthesis of [1,3]thiazolo[4,3- b][1,3,4]thiadiazoles: Correct Structure of the Products.
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- Chemistry of Heterocyclic Compounds, 2014, v. 49, n. 10, p. 1458, doi. 10.1007/s10593-014-1396-4
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Ring-Ring Tautomerism of the Products of the Reaction of 4-Hydroxytetrahydropyrimidine-2(1 H)-Thiones with Functionally Substituted Amines and Hydrazines.
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- Chemistry of Heterocyclic Compounds, 2014, v. 49, n. 10, p. 1490, doi. 10.1007/s10593-014-1400-z
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Oxidation of thioamides with the DMSO-HCl system: a convenient and efficient method for the synthesis of 1,2,4-thiadiazoles, isothiazolo-[5,4- b]pyridines, and heterocyclic disulfides.
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- Chemistry of Heterocyclic Compounds, 2013, v. 49, n. 4, p. 636, doi. 10.1007/s10593-013-1291-4
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Utility of 5-(furan-2-yl)-3-(p-tolyl)-4,5-dihydro-1H-pyrazole-1-carbothioamide in the synthesis of heterocyclic compounds with antimicrobial activity.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0566-y
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Indole bearing thiadiazole analogs: synthesis, β-glucuronidase inhibition and molecular docking study.
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- BMC Chemistry, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s13065-019-0522-x
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Synthesis and Study of Some 4-Chlorophenoxy Methyl Substituted amido1,3,4-Oxadiazoles, 1,3,4- Thiadiazoles and 1,2,4-Triazoles from 4-Chloro phenoxy acetic acid.
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- Journal of Education & Science, 2013, v. 26, n. 71, p. 47
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Synthesis , Identification and Antibactrial Activity of Some New Heterocyclic Compounds Contaning 1,3,4-Thiadiazole and 1,3,4-Oxadiazole Bearing Schiff Base.
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- Iraqi National Journal Of Chemistry, 2017, v. 17, n. 2, p. 103
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SYNTHETIC APPROACHES, CHEMICAL MODIFICATION AND BIOLOGICAL ACTIVITY OF NON-CONDENSED 1,3,4-THIADIAZOLE DERIVATIVES: A REVIEW.
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- Pharmacia (0428-0296), 2018, v. 65, n. 4, p. 72
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New benzothiazole hybrids as potential VEGFR-2 inhibitors: design, synthesis, anticancer evaluation, and in silico study.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2166036
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Synthesis, telomerase inhibitory and anticancer activity of new 2-phenyl-4H-chromone derivatives containing 1,3,4-oxadiazole moiety.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 345, doi. 10.1080/14756366.2020.1864630
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Design, synthesis, and anticancer evaluation of novel quinoline derivatives of ursolic acid with hydrazide, oxadiazole, and thiadiazole moieties as potent MEK inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 955, doi. 10.1080/14756366.2019.1605364
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Novel agonists of free fatty acid receptor 1 (GPR40) based on 3-(1,3,4-thiadiazol-2-yl)propanoic acid scaffold.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1404, doi. 10.3109/14756366.2016.1142984
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Salts of 5-amino-2-sulfonamide-1,3,4-thiadiazole, a structural and analog of acetazolamide, show interesting carbonic anhydrase inhibitory properties, diuretic, and anticonvulsant action.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1102, doi. 10.3109/14756366.2015.1096270
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Design, synthesis and biological evaluation of N -(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 174, doi. 10.1080/14756366.2016.1197221
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Spectrophotometric Determination of Methyldopa and Levodopa by Oxidative Coupling Reactions using the synthesis reagent (2- amino-5-(para-aminophenyl)-1,3,4-thiadiazole) and Investigation of Biological Activity.
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- Journal of Chemical Health Risks, 2024, v. 14, n. 2, p. 349, doi. 10.22034/JCHR.2024.1088080
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Interaction of 2-Amino-1,3,4-thiadiazoles with 1,2,4-Triazine-5-carbonitriles.
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- Doklady Chemistry, 2022, v. 504, n. 1, p. 79, doi. 10.1134/S0012500822600146
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Bis[1,3]thiazolo[4,5-f:5',4'-h]thieno[3,4-b]quinoxaline Derivatives as New Building Blocks of Polymers for Organic Electronics.
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- Doklady Chemistry, 2018, v. 482, n. 1, p. 207, doi. 10.1134/S0012500818090070
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Novel hybrid compounds based on amino derivatives of 1,2,4-thiadiazole and docosahexaenoic acid.
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- Doklady Chemistry, 2012, v. 447, n. 1, p. 238, doi. 10.1134/S0012500812110031
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Novel binary compounds derived from 1,2,4-thiadiazole.
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- Doklady Chemistry, 2012, v. 446, n. 1, p. 171, doi. 10.1134/S0012500812090017
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Novel 1,2,4-thiadiazoles with an NO-producing fragment.
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- Doklady Chemistry, 2010, v. 435, n. 2, p. 311, doi. 10.1134/S0012500810120013
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Efficient synthesis of novel thiadiazolo[2,3-b]quinazolin-6-ones catalyzed by diphenhydramine hydrochloride-CoCl<sub>2</sub>⋅6H<sub>2</sub>O deep eutectic solvent.
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- Scientific Reports, 2024, v. 14, n. 1, p. N.PAG, doi. 10.1038/s41598-024-52017-3
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