Works matching AU Gul, Halise Inci
Results: 53
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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Synthesis and biological evaluation of new pyrazolebenzene-sulphonamides as potential anticancer agents and hCA I and II inhibitors.
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- Turkish Journal of Chemistry, 2021, v. 45, n. 3, p. 528, doi. 10.3906/kim-2009-37
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Synthesis and pharmacological effects of novel benzenesulfonamides carrying benzamide moiety as carbonic anhydrase and acetylcholinesterase inhibitors.
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- Turkish Journal of Chemistry, 2020, v. 44, n. 6, p. 1601, doi. 10.3906/kim-2007-37
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Synthesis and bioactivities of 1-(4-hydroxyphenyl)-2-((heteroaryl)thio)ethanones as carbonic anhydrase I, II and acetylcholinesterase inhibitors.
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- Turkish Journal of Chemistry, 2020, v. 44, n. 4, p. 1058, doi. 10.3906/kim-2004-36
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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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Microwave-assisted synthesis and bioevaluation of new sulfonamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 369, doi. 10.1080/14756366.2016.1254207
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Synthesis, carbonic anhydrase I and II inhibition studies of the 1,3,5-trisubstituted-pyrazolines.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 189, doi. 10.1080/14756366.2016.1244533
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Designing, synthesis and bioactivities of 4-[3-(4-hydroxyphenyl)-5-aryl-4,5-dihydro-pyrazol-1-yl]benzenesulfonamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 169, doi. 10.1080/14756366.2016.1243536
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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, cytotoxicity and carbonic anhydrase inhibitory activities of new pyrazolines.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 20, doi. 10.1080/14756366.2016.1217852
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- Article
Synthesis and bioactivity studies of 1-aryl-3-(2-hydroxyethylthio)-1- propanones.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 105, doi. 10.1080/14756366.2016.1209495
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Synthesis and bioactivity studies of 1-aryl-3-(2-hydroxyethylthio)-1-propanones.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 105, doi. 10.1080/14756366.2016.1209495
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Synthesis and bioactivity studies on new 4-(3-(4-Substitutedphenyl)-3a,4-dihydro-3 H -indeno[1,2-c]pyrazol-2-yl) benzenesulfonamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1619, doi. 10.3109/14756366.2016.1160077
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Inhibitory effects of benzimidazole containing new phenolic Mannich bases on human carbonic anhydrase isoforms hCA I and II.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1540, doi. 10.3109/14756366.2016.1156675
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Inhibitory effects of isatin Mannich bases on carbonic anhydrases, acetylcholinesterase, and butyrylcholinesterase.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1498, doi. 10.3109/14756366.2016.1149479
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Carbonic anhydrase inhibition and cytotoxicity studies of Mannich base derivatives of thymol.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1375, doi. 10.3109/14756366.2016.1140755
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The inhibitory effects of phenolic Mannich bases on carbonic anhydrase I and II isoenzymes.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1678, doi. 10.3109/14756366.2015.1126715
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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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Synthesis and carbonic anhydrase inhibitory activities of new thienyl-substituted pyrazoline benzenesulfonamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 1, doi. 10.1080/14756366.2016.1181627
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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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Synthesis of some acrylophenones with N -methylpiperazine and evaluation of their cytotoxicities.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 1, p. 147, doi. 10.3109/14756366.2015.1014474
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- Article
Synthesis of 3-aroyl-4-aryl-1-isopropylamino-4-piperidinols and evaluation of the cytotoxicities of the compounds against human hepatoma and breast cancer cell lines.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 4, p. 564, doi. 10.3109/14756366.2014.951350
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Synthesis and biological evaluation of 1,5-bis(4-hydroxy-3-methoxyphenyl)penta-1,4-dien-3-one and its aminomethyl derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 3, p. 383, doi. 10.3109/14756366.2014.940934
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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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Cytotoxic activity of 4′-hydroxychalcone derivatives against Jurkat cells and their effects on mammalian DNA topoisomerase I.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2009, v. 24, n. 3, p. 804, doi. 10.1080/14756360802399126
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- Article
Synthesis and Antifungal Activity of 1-Aryl-3-phenethylamino-1-propanone Hydrochlorides and 3-Aroyl-4-aryl-1-phenethyl-4-piperidinols.
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- Archiv der Pharmazie, 2010, v. 343, n. 5, p. 291, doi. 10.1002/ardp.200900136
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- Article
Evaluation of Antimicrobial Activities of Several Mannich Bases and Their Derivatives.
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- Archiv der Pharmazie, 2005, v. 338, n. 7, p. 335, doi. 10.1002/ardp.200400962
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Energy absorption buildup factors of some potential bioactive compounds in the energy region 0.015–15 MeV.
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- Spectroscopy Letters, 2017, v. 50, n. 6, p. 301, doi. 10.1080/00387010.2017.1320764
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Obesity and Obesity-Related Diseases and Treatments.
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- Pharmata, 2023, v. 3, n. 3, p. 64, doi. 10.5152/Pharmata.2023.1321447
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- Article
Inhibitory effects of the chalcones towards carbonic anhydrase I, II and acetylcholinesterase enzymes.
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- Erzincan University Journal of Science & Technology, 2020, v. 13, n. 3, p. 1138, doi. 10.18185/erzifbed.748798
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IMIDAZOLINONE-BASED SULFONAMIDE DERIVATIVES: SYNTHESIS, CHARACTERIZATION, AND INHIBITORY PROPERTY AGAINST SOME METABOLIC ENZYMES.
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- Journal of Faculty of Pharmacy of Ankara University / Ankara Üniversitesi Eczacilik Fakültesi Dergisi, 2023, v. 47, n. 3, p. 915, doi. 10.33483/jfpau.1311157
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- Article
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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- Article
Crystal structure of ( E)-2-({4-hydroxy-5-methoxy-3-[(4-methyl-1-piperazinyl)methyl]phenyl} methylidene)-1-indanone, C<sub>23</sub>H<sub>26</sub>N<sub>2</sub>O<sub>3</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2017, v. 232, n. 1, p. 113, doi. 10.1515/ncrs-2016-0176
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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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Crystal structure of 3-(thiophen-2-yl-carbonyl)-4-(thiophen-2-yl)-1-isopropyl-4-piperidinol, C<sub>17</sub>H<sub>21</sub>NO<sub>2</sub>S<sub>2</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2013, v. 228, n. 3, p. 355, doi. 10.1524/ncrs.2013.0176
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Crystal structure of 3-(p-bromobenzoyl)-4-(p-bromophenyl)-1-isopropyl-4-piperidinol hydrochloride, C<sub>21</sub>H<sub>24</sub>Br<sub>2</sub>ClNO<sub>2</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2013, v. 228, n. 3, p. 381, doi. 10.1524/ncrs.2013.0190
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Synthesis, molecular modeling, and biological evaluation of 4‐[5‐aryl‐3‐(thiophen‐2‐yl)‐4,5‐dihydro‐1<italic>H</italic>‐pyrazol‐1‐yl] benzenesulfonamides toward acetylcholinesterase, carbonic anhydrase I and II enzymes
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- Chemical Biology & Drug Design, 2018, v. 91, n. 4, p. 854, doi. 10.1111/cbdd.13149
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Higher number of microplastics in tumoral colon tissues from patients with colorectal adenocarcinoma.
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- Environmental Chemistry Letters, 2023, v. 21, n. 2, p. 639, doi. 10.1007/s10311-022-01560-4
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- Article
Deciphering binding mechanism between bovine serum albumin and new pyrazoline compound K4.
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- Luminescence: Journal of Biological & Chemical Luminescence, 2020, v. 35, n. 4, p. 534, doi. 10.1002/bio.3762
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Monoamine Oxidase (MAO) as a Potential Target for Anticancer Drug Design and Development.
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- Molecules, 2021, v. 26, n. 19, p. 6019, doi. 10.3390/molecules26196019
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- Article
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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- Article
In Vitro Enzyme Activity and Molecular Docking Studies of Pyrazoline Derivatives as Monoamine Oxidase Inhibitors.
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- Pharmaceutical Chemistry Journal, 2024, v. 58, n. 3, p. 419, doi. 10.1007/s11094-024-03161-7
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Biological Activities and Drug-Likeness Properties of Phenol-Based Heterocyclic Compounds.
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- Pharmaceutical Chemistry Journal, 2024, v. 57, n. 11, p. 1754, doi. 10.1007/s11094-024-03076-3
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- Article
Evaluation of the anti-inflammatory activity of N, N′-bis(3-dimethylamino-1-phenyl-propylidene)hydrazine dihydrochloride.
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- Pharmaceutical Biology, 2009, v. 47, n. 10, p. 968, doi. 10.1080/13880200902967961
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- Article
Synthesis and in vitro carbonic anhydrases and acetylcholinesterase inhibitory activities of novel imidazolinone‐based benzenesulfonamides.
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- Archiv der Pharmazie, 2021, v. 354, n. 4, p. 1, doi. 10.1002/ardp.202000375
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Synthesis of benzamide derivatives with thiourea‐substituted benzenesulfonamides as carbonic anhydrase inhibitors.
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- Archiv der Pharmazie, 2021, v. 354, n. 2, p. 1, doi. 10.1002/ardp.202000230
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- Article
Biological Evaluation and Structure-Activity Relationships of Bis-(3-aryl-3-oxo-propyl)-methylamine Hydrochlorides and 4-Aryl-3- arylcarbonyl-1-methyl-4-piperidinol Hy-drochlorides as Potential Cytotoxic Agents and their Alkylating Ability towards...
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- Drug Research / Arzneimittel-Forschung (Editio Cantor Verlag fur Medizin und Naturwissenschaften), 2005, v. 55, n. 6, p. 332
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- Article
Acetylcholinesterase inhibitory potencies of new pyrazoline derivatives.
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- Journal of Research in Pharmacy, 2020, v. 24, n. 4, p. 464, doi. 10.35333/jrp.2020.194
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- Article