Works matching DE "CHALCONE"
Results: 1015
Reaction of Substituted Chalcone with Guanidine in the Presence of Hydrogen Peroxide.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 12, p. 2504, doi. 10.1134/S107042802412025X
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Cytotoxic and apoptotic effect of chalcone 5 on mouse colon cancer cells CT-26.
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- Indian Journal of Biochemistry & Biophysics, 2024, v. 61, n. 3, p. 145, doi. 10.56042/ijbb.v61i3.4446
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含氟芳香查尔酮衍生物的合成与三阶非线性光学性质.
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- Chinese Journal of Applied Chemistry, 2025, v. 42, n. 1, p. 86, doi. 10.19894/j.issn.1000-0518.240208
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Chalcone Derivatives: Synthesis and Cytotoxicity Assays.
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- Al-Nahrain Journal of Science, 2024, v. 27, n. 5, p. 10, doi. 10.22401/ANJS.27.5.02
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Targeted inhibition of PqsR in Pseudomonas aeruginosa PAO1 quorum-sensing network by chalcones as promising antibacterial compounds.
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- Molecular Biology Reports, 2025, v. 52, n. 1, p. 1, doi. 10.1007/s11033-025-10270-3
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DFT and Molecular Docking Studies of Two Heterocyclic Chalcone Derivatives.
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- Macromolecular Symposia, 2024, v. 413, n. 1, p. 1, doi. 10.1002/masy.202200226
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Sodium Alginate Biopolymer: An Efficient, Recyclable Green Catalyst for the Synthesis of Chalcone Derivatives under Mild Conditions.
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- Macromolecular Symposia, 2022, v. 404, n. 1, p. 1, doi. 10.1002/masy.202100428
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- Article
Cobalt Ferrite MNPs: An Efficient and Robust Catalyst for Synthesis of 1,3,5‐Trisubstituted Pyrazolines.
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- Macromolecular Symposia, 2021, v. 400, n. 1, p. 1, doi. 10.1002/masy.202100062
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Optical Characterization of Chalcone‐Doped PMMA Thin Films for Photonic Applications Using Spectroscopic Technique of Drop Casting Method.
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- Macromolecular Symposia, 2020, v. 392, n. 1, p. 1, doi. 10.1002/masy.202000165
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- Article
Performance of density functional theory for calculating the electronic, static, and dynamic nonlinear optical properties of asymmetric (3E,5E)-3,5-dibenzylidene-piperidin-4-one derivatives.
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- Optical & Quantum Electronics, 2023, v. 55, n. 12, p. 1, doi. 10.1007/s11082-023-05383-7
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Spectral and ASE properties of an amino chalcone 1-phenyl-3-[4-(1-pyrrolidinyl) phenyl]-(2E)-propen-1-one.
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- Optical & Quantum Electronics, 2020, v. 52, n. 3, p. 1, doi. 10.1007/s11082-020-2249-2
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- Article
A novel aldo–keto reductase gene is involved in 6′-deoxychalcone biosynthesis in dahlia (Dahlia variabilis).
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- Planta: An International Journal of Plant Biology, 2022, v. 256, n. 3, p. 1, doi. 10.1007/s00425-022-03958-4
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Chalcone synthases (CHSs): the symbolic type III polyketide synthases.
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- Planta: An International Journal of Plant Biology, 2020, v. 251, n. 1, p. N.PAG, doi. 10.1007/s00425-019-03307-y
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Soybean chalcone isomerase: evolution of the fold, and the differential expression and localization of the gene family.
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- Planta: An International Journal of Plant Biology, 2015, v. 241, n. 2, p. 507, doi. 10.1007/s00425-014-2200-5
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A New Chalcone from the Heartwood of Dalbergia cochinchinensis.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 3, p. 405, doi. 10.1007/s10600-016-1659-7
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Synthesis of 3-amino-6-methyl-4-phenylpyridin-2(1 H)-one and its derivatives.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 2, p. 186, doi. 10.1007/s10593-017-2038-4
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Synthesis and Tuberculostatic Activity of Pyrrolyl and Pyrazolinyl Podands.
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- Chemistry of Heterocyclic Compounds, 2014, v. 50, n. 7, p. 946, doi. 10.1007/s10593-014-1549-5
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Pharmacological potential of 4-dimethylamino chalcone against acute and neuropathic pain in mice.
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- Journal of Pharmacy & Pharmacology, 2024, v. 76, n. 8, p. 983, doi. 10.1093/jpp/rgae057
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QSAR ANALYSIS USING SEMI-EMPIRICAL AM1 METHOD, MOLECULAR DOCKING, AND ADMET STUDIES OF CHALCONE DERIVATIVES AS ANTIMALARIAL COMPOUNDS.
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- Jurnal Kimia Riset, 2023, v. 8, n. 2, p. 186, doi. 10.20473/jkr.v8i2.51798
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WATER ROLE ON DIELS-ALDER REACTION OF PRENYLATED FLAVONOID FORMATION IN Boesenbergia pandurata: MECHANISM STUDY.
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- Jurnal Kimia Riset, 2023, v. 8, n. 2, p. 131, doi. 10.20473/jkr.v8i2.45215
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The Synthesis and Anticancer Activities of Ferrocenyl Chalcones; Drug-Likeness Calculations.
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- International Journal of Engineering Research & Development (IJERAD), 2021, v. 13, n. 2, p. 690, doi. 10.29137/umagd.927358
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Synthesis and Study of Many New Chalcone Derivatives.
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- Journal of Education & Science, 2018, v. 27, n. 4, p. 1
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Actividad antiproliferativa de una chalcona aislada de chromolaena tacotana y su relación con apoptosis y autofagia.
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- Repertorio de Medicina y Cirugía, 2023, v. 32, p. 61, doi. 10.31260/RepertMedCir.01217372.1584
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- Article
Isoliquiritigenin ameliorates advanced glycation end‐products toxicity on renal proximal tubular epithelial cells.
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- Environmental Toxicology, 2022, v. 37, n. 8, p. 2096, doi. 10.1002/tox.23553
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Synthesis, Spectral Characterization and Anticancer Study of BioComplexes Pd from Methyl Imidazole.
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- Onkologia i Radioterapia, 2023, v. 17, n. 12, p. 1
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Synthesis of chalcone derivatives with methoxybenzene and pyridine moieties as potential antimalarial agents.
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- Pharmacia (0428-0296), 2023, v. 70, n. 4, p. 1305, doi. 10.3897/pharmacia.70.e107406
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Molecular docking and dynamics analysis of halogenated imidazole chalcone as anticancer compounds.
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- Pharmacia (0428-0296), 2023, v. 70, n. 2, p. 323, doi. 10.3897/pharmacia.70.e101989
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A geranylated chalcone with antiplatelet activity from the leaves of breadfruit (Artocarpus altilis).
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- Pharmacia (0428-0296), 2020, v. 67, n. 4, p. 173, doi. 10.3897/pharmacia.67.e56788
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Correction: A study on catalytic and non-catalytic sites of H5N1 and H1N1 neuraminidase as the target for chalcone inhibitors.
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- Applied Biological Chemistry, 2023, v. 66, n. 1, p. 1, doi. 10.1186/s13765-023-00809-y
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Design, synthesis, and biological evaluation of chalcones for anticancer properties targeting glycogen synthase kinase 3 beta.
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- Applied Biological Chemistry, 2022, v. 65, n. 1, p. 1, doi. 10.1186/s13765-022-00686-x
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A study on catalytic and non-catalytic sites of H5N1 and H1N1 neuraminidase as the target for chalcone inhibitors.
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- Applied Biological Chemistry, 2021, v. 64, n. 1, p. 1, doi. 10.1186/s13765-021-00639-w
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Novel N-Arylmethyl-aniline/chalcone hybrids as potential VEGFR inhibitors: synthesis, biological evaluations, and molecular dynamic simulations.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2278022
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Novel 3-(6-methylpyridin-2-yl)coumarin-based chalcones as selective inhibitors of cancer-related carbonic anhydrases IX and XII endowed with anti-proliferative activity.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 1043, doi. 10.1080/14756366.2022.2056734
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New 1,2,3-triazole linked ciprofloxacin-chalcones induce DNA damage by inhibiting human topoisomerase I& II and tubulin polymerization.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 1346, doi. 10.1080/14756366.2022.2072308
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Identification of novel non-toxic and anti-angiogenic α-fluorinated chalcones as potent colchicine binding site inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 339, doi. 10.1080/14756366.2021.2014831
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Discovery of benzochalcone derivative as a potential antigastric cancer agent targeting signal transducer and activator of transcription 3 (STAT3).
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 2004, doi. 10.1080/14756366.2022.2100366
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Design, synthesis, and evaluation of chalcone-Vitamin E-donepezil hybrids as multi-target-directed ligands for the treatment of Alzheimer's disease.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 69, doi. 10.1080/14756366.2021.1993845
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A review on synthetic chalcone derivatives as tubulin polymerisation inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 9, doi. 10.1080/14756366.2021.1976772
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Novel chalcone/aryl carboximidamide hybrids as potent anti-inflammatory via inhibition of prostaglandin E2 and inducible NO synthase activities: design, synthesis, molecular docking studies and ADMET prediction.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 1067, doi. 10.1080/14756366.2021.1929201
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Novel piperazine–chalcone hybrids and related pyrazoline analogues targeting VEGFR-2 kinase; design, synthesis, molecular docking studies, and anticancer evaluation.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 308, doi. 10.1080/14756366.2020.1861606
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Discovery of orally active chalcones as histone lysine specific demethylase 1 inhibitors for the treatment of leukaemia.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 207, doi. 10.1080/14756366.2020.1852556
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Analogues of 2′-hydroxychalcone with modified C4-substituents as the inhibitors against human acetylcholinesterase.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 130, doi. 10.1080/14756366.2020.1847100
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Design, synthesis, and evaluation of 1, 4-benzodioxan-substituted chalcones as selective and reversible inhibitors of human monoamine oxidase B.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2020, v. 35, n. 1, p. 1513, doi. 10.1080/14756366.2020.1797711
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2-Thiopyrimidine/chalcone hybrids: design, synthesis, ADMET prediction, and anticancer evaluation as STAT3/STAT5a inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2020, v. 35, n. 1, p. 864, doi. 10.1080/14756366.2020.1740922
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Design, synthesis, molecular modelling and biological evaluation of novel 3-(2-naphthyl)-1-phenyl-1H-pyrazole derivatives as potent antioxidants and 15-Lipoxygenase inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2020, v. 35, n. 1, p. 847, doi. 10.1080/14756366.2020.1742116
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Synthesis, biological evaluation, and molecular modelling of new naphthalene-chalcone derivatives as potential anticancer agents on MCF-7 breast cancer cells by targeting tubulin colchicine binding site.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2020, v. 35, n. 1, p. 139, doi. 10.1080/14756366.2019.1690479
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Synthesis, cytotoxicities, and carbonic anhydrase inhibition potential of 6-(3-aryl-2-propenoyl)-2(3H)-benzoxazolones.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1722, doi. 10.1080/14756366.2019.1670657
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SAR and molecular mechanism studies of monoamine oxidase inhibition by selected chalcone analogs.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 863, doi. 10.1080/14756366.2019.1593158
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Computational screening of chalcones acting against topoisomerase IIα and their cytotoxicity towards cancer cell lines.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 134, doi. 10.1080/14756366.2018.1507029
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Chalcones isolated from Angelica keiskei inhibit cysteine proteases of SARS-CoV.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 1, p. 23, doi. 10.3109/14756366.2014.1003215
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