Works matching AU Bilginer, Sinan
Results: 17
Antibacterial and Acetylcholinesterase Inhibitory Potentials of Triazenes Containg Sulfonamide Moiety.
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- Pharmaceutical Chemistry Journal, 2021, v. 55, n. 3, p. 284, doi. 10.1007/s11094-021-02412-1
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Novel Mannich bases with strong carbonic anhydrases and acetylcholinesterase inhibition effects: 3-(aminomethyl)-6-{3-[4-(trifluoromethyl)phenyl]acryloyl}-2(3H)-benzoxazolones.
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- Turkish Journal of Chemistry, 2021, v. 45, n. 3, p. 805, doi. 10.3906/kim-2101-25
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Novel sulphonamides incorporating triazene moieties show powerful carbonic anhydrase I and II inhibitory properties.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2020, v. 35, n. 1, p. 325, doi. 10.1080/14756366.2019.1700240
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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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Synthesis of 4-(2-substituted hydrazinyl)benzenesulfonamides and their carbonic anhydrase inhibitory effects.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 4, p. 568, doi. 10.3109/14756366.2015.1047359
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Carbonic anhydrase inhibitors. Phenols incorporating 2- or 3-pyridyl-ethenylcarbonyl and tertiary amine moieties strongly inhibit Saccharomyces cerevisiae β-carbonic anhydrase.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 4, p. 495, doi. 10.3109/14756366.2013.806497
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1-(3-Aminomethyl-4-hydroxyphenyl)-3-pyridinyl-2-propen-1-ones: A novel group of tumour-selective cytotoxins.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2013, v. 28, n. 5, p. 974, doi. 10.3109/14756366.2012.700927
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Oleuropein and Verbascoside - Their Inhibition Effects on Carbonic Anhydrase and Molecular Docking Studies.
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- Journal of Oleo Science, 2021, v. 70, n. 9, p. 1275, doi. 10.5650/jos.ess21106
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Evaluation of antioxidant potentials and acetylcholinesterase inhibitory effects of some new salicylic acid-salicylamide hybrids.
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- Journal of the Iranian Chemical Society, 2023, v. 20, n. 7, p. 1535, doi. 10.1007/s13738-023-02775-0
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Effects of a Novel Benzenesulfonamide 4-(3-(4-Bromophenyl)-5-(2,4-dimethoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl) on Antioxidant Enzymes and Hematological Parameters of Rainbow Trout (Oncorhynchus mykiss).
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- Pakistan Journal of Zoology, 2021, v. 53, n. 6, p. 2083, doi. 10.17582/journal.pjz/20191118081134
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Crystal structure of 4-[5-(4-fluorophenyl)-3-(4-hydroxyphenyl)-4,5-dihydropyrazol-1-yl] benzenesulfonamide, C<sub>21</sub>H<sub>18</sub>FN<sub>3</sub>O<sub>3</sub>S.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2016, v. 231, n. 1, p. 81, doi. 10.1515/ncrs-2015-0034
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New benzamide derivatives and their nicotinamide/cinnamamide analogs as cholinesterase inhibitors.
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- Molecular Diversity, 2022, v. 26, n. 2, p. 1201, doi. 10.1007/s11030-021-10249-9
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Synthesis and Antifungal Evaluation of 1-Aryl-2-dimethylaminomethyl-2-propen-1-one Hydrochlorides.
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- Molecules, 2011, v. 16, n. 6, p. 4660, doi. 10.3390/molecules16064660
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Synthesis and in silico studies of triazene‐substituted sulfamerazine derivatives as acetylcholinesterase and carbonic anhydrases inhibitors.
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- Archiv der Pharmazie, 2021, v. 354, n. 1, p. 1, doi. 10.1002/ardp.202000243
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New halogenated chalcones with cytotoxic and carbonic anhydrase inhibitory properties: 6‐(3‐Halogenated phenyl‐2‐propen‐1‐oyl)‐2(3H)‐benzoxazolones.
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- Archiv der Pharmazie, 2020, v. 353, n. 6, p. 1, doi. 10.1002/ardp.201900384
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Molecular Docking Study of Several Seconder Metabolites from Medicinal Plants as Potential Inhibitors of COVID-19 Main Protease.
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- Turkish Journal of Pharmaceutical Sciences, 2022, v. 19, n. 4, p. 431, doi. 10.4274/tjps.galenos.2021.83548
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Phenothiazine‐based chalcones as potential dual‐target inhibitors toward cholinesterases (AChE, BuChE) and monoamine oxidases (MAO‐A, MAO‐B).
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- Journal of Heterocyclic Chemistry, 2021, v. 58, n. 1, p. 161, doi. 10.1002/jhet.4156
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