Works matching DE "CHALCONES"
Results: 971
Production of Hydroxlated Flavonoids with Cytochrome P450 BM3 Variant F87V and Their Antioxidative Activities.
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- Bioscience, Biotechnology & Biochemistry, 2013, v. 77, n. 6, p. 1340, doi. 10.1271/bbb.130148
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Six New Chalcones from Angelica keiskei Inducing Adiponectin Production in 3T3-L1 Adipocytes.
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- Bioscience, Biotechnology & Biochemistry, 2012, v. 76, n. 5, p. 961, doi. 10.1271/bbb.110976
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Mid-Miocene divergence of Ionopsidium and Cochlearia and its impact on the systematics and biogeography of the tribe Cochlearieae (Brassicaceae).
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- Taxon, 2012, v. 61, n. 1, p. 76, doi. 10.1002/tax.611006
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Synthesis of One‐Component Type II Visible‐Light‐Absorbing Chalcones Containing Fused Aromatic Rings and Investigation of Free Radical Photopolymerization Properties.
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- Macromolecular Chemistry & Physics, 2024, v. 225, n. 9, p. 1, doi. 10.1002/macp.202300428
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Nickel‐Catalyzed Chemodivergent Coupling of Alcohols: Efficient Routes to Access α,α‐Disubstituted Ketones and α‐Substituted Chalcones.
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- Chemistry - A European Journal, 2024, v. 30, n. 15, p. 1, doi. 10.1002/chem.202304082
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In situ Light‐Writable Orientation Control in Liquid Crystal Elastomer Film Enabled by Chalcones.
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- Angewandte Chemie, 2024, v. 136, n. 11, p. 1, doi. 10.1002/ange.202319698
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Regio‐ and Chemoselective Formal (4+1) Carbocyclization of Chalcones with Internal Alkynes via Rhodium(III) Catalysis.
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- Angewandte Chemie, 2023, v. 135, n. 30, p. 1, doi. 10.1002/ange.202305983
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Characterization and mapping of a QTL derived from Solanum habrochaites associated with elevated rutin content (quercetin-3-rutinoside) in tomato.
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- Euphytica, 2014, v. 200, n. 3, p. 441, doi. 10.1007/s10681-014-1180-7
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Inhibition of Kv1.3 Channels in Human Jurkat T Cells by Xanthohumol and Isoxanthohumol.
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- Journal of Membrane Biology, 2015, v. 248, n. 4, p. 705, doi. 10.1007/s00232-015-9782-0
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- Article
Design, Synthesis and In Vivo Anxiolytic Activity of Novel Flavonoids.
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- Pharmaceutical Chemistry Journal, 2021, v. 55, n. 9, p. 908, doi. 10.1007/s11094-021-02514-w
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Synthesis and α-Amylase Inhibition Studies of Some Coumarin Derivatives.
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- Pharmaceutical Chemistry Journal, 2018, v. 52, n. 6, p. 526, doi. 10.1007/s11094-018-1853-y
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Synthesis, Spectroscopic Studies, Antibacterial Activity, and Colorimetric Evaluation of the Time-Killing Assay for Newly Synthesized Chalcones Using Resazurin.
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- Pharmaceutical Chemistry Journal, 2018, v. 52, n. 6, p. 518, doi. 10.1007/s11094-018-1852-z
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- Article
Structural characterization and nonlinear optical properties of 1-phenyl-3-(4-bis(2-chloroethyl)aminophenyl)-2-propen-1-one.
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- Journal of Structural Chemistry, 2015, v. 56, n. 7, p. 1398, doi. 10.1134/S0022476615070227
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Conformational variability in a new terpenoid-like bischalcone: Structure and theoretical studies.
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- Journal of Structural Chemistry, 2013, v. 54, n. 6, p. 1112, doi. 10.1134/S0022476613060164
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Crystal structure of 1-(4-chlorophenyl)-3-{4-[2-(5-ethyl-pyridin-2-yl)-ethoxy]-phenyl}-propenone.
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- Journal of Structural Chemistry, 2013, v. 54, n. 3, p. 645, doi. 10.1134/S0022476613030293
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Synthesis of New Oxazepine and Thaizolidine Compounds derived from Pyrimidine-2(1H)-one.
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- Journal of Education & Science, 2020, v. 29, n. 2, p. 186, doi. 10.33899/edusj.2019.125908.1004
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Synthesis of New Heterocyclic Polymers from Chalcone.
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- Iraqi National Journal Of Chemistry, 2017, v. 17, n. 1, p. 18, doi. 10.22317/iqnjc.06201701
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Synthesis of some novel Heterocyclic Chalcone Derivatives.
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- Al-Qadisiyah Journal of Pure Science, 2018, v. 23, n. 2, p. 221, doi. 10.29350/jops.2018.23.2.755
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Synthesis and Characterization some Novel Heterocyclic Compounds of Pyrimidine and pyrazole from Chalcone derivatives.
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- Al-Qadisiyah Journal of Pure Science, 2018, v. 23, n. 2, p. 141, doi. 10.29350/jops.2018.23.2.747
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Design, synthesis, and enzyme inhibition evaluation of some novel Mono- and Di-O-ß-D-Glycopyranosyl Chalcone analogues with molecular docking studies.
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- Turkish Journal of Chemistry, 2023, v. 47, n. 1, p. 171, doi. 10.55730/1300-0527.3527
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Biological evaluation and synthesis of new pyrimidine-2(1H)-ol/-thiol derivatives derived from chalcones using the solid phase microwave method.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 2, p. 520, doi. 10.3906/kim-1711-9
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Synthesis and biological evaluation of novel chalcones bearing morpholine moiety as antiproliferative agents.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 2, p. 482, doi. 10.3906/kim-1705-28
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Tetrahydronaphthalene as a precursor of new series of chalcones, avanones, and avones.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 2, p. 237, doi. 10.3906/kim-1612-2
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Synthesis and in vitro anticancer evaluation of 1,4-phenylene-bis-pyrimidine-2-amine derivatives.
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- Turkish Journal of Chemistry, 2017, v. 41, n. 2, p. 263, doi. 10.3906/kim-1603-112
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Synthetic protocols on 6H-benzo[c]chromen-6-ones: a review.
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- Turkish Journal of Chemistry, 2016, v. 40, n. 1, p. 1, doi. 10.3906/kim-1504-67
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QSAR study of chalcone derivatives as anti-Leishmania agents.
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- Turkish Journal of Chemistry, 2014, v. 38, n. 5, p. 716, doi. 10.3906/kim-1307-33
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In silico screening of chalcones and flavonoids as potential inhibitors against yellow head virus 3C-like protease.
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- PeerJ, 2023, p. 1, doi. 10.7717/peerj.15086
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Acidic Ionic Liquids in Ultrasonic Irradiation Conditions Promote the Nucleophilic Addition to Chalcone Derivatives.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 8, p. 5099, doi. 10.1080/10406638.2023.2259572
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Design, Synthesis, Crystal Structure, Biological Activity and Molecular Modeling of Novel Schiff Bases Derived from Chalcones and 5-Hydrazino-1,3-Dimethyl-4-Nitropyrazole as Anticancer Agents.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 6, p. 4178, doi. 10.1080/10406638.2023.2247118
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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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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 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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Morpholine-based chalcones as dual-acting monoamine oxidase-B and acetylcholinesterase inhibitors: synthesis and biochemical investigations.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 188, doi. 10.1080/14756366.2020.1842390
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Antiproliferative activity and p53 upregulation effects of chalcones on human breast cancer cells.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1093, doi. 10.1080/14756366.2019.1615485
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Synthesis, antimicrobial, anti-biofilm evaluation, and molecular modelling study of new chalcone linked amines derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 818, doi. 10.1080/14756366.2018.1461855
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Design of potent fluoro-substituted chalcones as antimicrobial agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 490, doi. 10.1080/14756366.2016.1265517
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Synthesis and bioactivities of halogen bearing phenolic chalcones and their corresponding bis Mannich bases.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 125, doi. 10.1080/14756366.2016.1221825
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Synthesis, cyclooxygenase inhibition and anti-inflammatory evaluation of new 1,3,5-triaryl-4,5-dihydro-1 H -pyrazole derivatives possessing methanesulphonyl pharmacophore.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1545, doi. 10.3109/14756366.2016.1158168
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Niacin esters of chalcones with tumor-selective properties.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1451, doi. 10.3109/14756366.2016.1144595
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Synthesis of mono Mannich bases of 2-(4-hydroxybenzylidene)-2,3-dihydroinden-1-one and evaluation of their cytotoxicities.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 5, p. 818, doi. 10.3109/14756366.2015.1070263
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Design, synthesis and preliminary structure–activity relationship investigation of nitrogen-containing chalcone derivatives as acetylcholinesterase and butyrylcholinesterase inhibitors: a further study based on Flavokawain B Mannich base derivatives
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 4, p. 580, doi. 10.3109/14756366.2015.1050009
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Simple chalcones and bis -chalcones ethers as possible pleiotropic agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 2, p. 302, doi. 10.3109/14756366.2015.1021253
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Antitumor evaluation and molecular docking study of substituted 2-benzylidenebutane-1,3-dione, 2-hydrazonobutane-1,3-dione and trifluoromethyl-1H-pyrazole analogues.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 4, p. 679, doi. 10.3109/14756366.2014.960863
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Synthesis, characterization and biological evaluation of novel 4′-fluoro-2′-hydroxy-chalcone derivatives as antioxidant, anti-inflammatory and analgesic agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 3, p. 484, doi. 10.3109/14756366.2014.949255
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Synthetic compounds from an in house library as inhibitors of falcipain-2 from Plasmodium falciparum.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 2, p. 299, doi. 10.3109/14756366.2014.920839
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Design, synthesis, characterization and in vitro and in vivo anti-inflammatory evaluation of novel pyrazole-based chalcones.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 1, p. 22, doi. 10.3109/14756366.2013.873037
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- Article
Synthesis and biological evaluation of ( E)-1-(substituted)-3-phenylprop-2-en-1-ones bearing rhodanines as potent anti-microbial agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 5, p. 647, doi. 10.3109/14756366.2013.837899
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Synthesis and antimalarial activity of urenyl Bis-chalcone in vitro and in vivo.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2013, v. 28, n. 6, p. 1267, doi. 10.3109/14756366.2012.733383
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Synthesis and theoretical calculations of carbazole substituted chalcone urea derivatives and studies their polyphenol oxidase enzyme activity.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2013, v. 28, n. 4, p. 808, doi. 10.3109/14756366.2012.688040
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Synthesis of novel carbazole chalcones as radical scavenger, antimicrobial and cancer chemopreventive agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2013, v. 28, n. 3, p. 593, doi. 10.3109/14756366.2012.663365
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