Works by Akdemir, Atilla
Results: 31
New azolyl-derivatives as multitargeting agents against breast cancer and fungal infections: synthesis, biological evaluation and docking study.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 1631, doi. 10.1080/14756366.2021.1954918
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- Article
Design, synthesis and biological activity of selective hCAs inhibitors based on 2-(benzylsulfinyl)benzoic acid scaffold.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1400, doi. 10.1080/14756366.2019.1651315
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- Article
Fibrate-based N-acylsulphonamides targeting carbonic anhydrases: synthesis, biochemical evaluation, and docking studies.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1051, doi. 10.1080/14756366.2019.1611801
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- Article
Novel 2-indolinones containing a sulfonamide moiety as selective inhibitors of candida β-carbonic anhydrase enzyme.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 528, doi. 10.1080/14756366.2018.1564045
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Novel thiazolidinone-containing compounds, without the well-known sulphonamide zinc-binding group acting as human carbonic anhydrase IX inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 1299, doi. 10.1080/14756366.2018.1499628
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Open saccharin-based secondary sulfonamides as potent and selective inhibitors of cancer-related carbonic anhydrase IX and XII isoforms.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 51, doi. 10.1080/14756366.2016.1235040
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Computational investigation of the selectivity of salen and tetrahydrosalen compounds towards the tumor-associated hCA XII isozyme.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 1, p. 114, doi. 10.3109/14756366.2014.892936
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Synthesis and Functional Investigations of Computer Designed Novel Cladribine-Like Compounds for the Treatment of Multiple Sclerosis.
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- Archiv der Pharmazie, 2017, v. 350, n. 11, p. n/a, doi. 10.1002/ardp.201700185
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- Article
Aromatase inhibition by 2-methyl indole hydrazone derivatives evaluated via molecular docking and in vitro activity studies.
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- Xenobiotica, 2019, v. 49, n. 5, p. 549, doi. 10.1080/00498254.2018.1482029
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- Article
A Study On Synthesis, Biological Activities and Molecular Modelling of Some Novel Trisubstituted 1,2,4‐Triazole Derivatives.
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- ChemistrySelect, 2018, v. 3, n. 31, p. 8813, doi. 10.1002/slct.201801578
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- Article
Synthesis of flurbiprofen thiadiazole urea derivatives and assessment of biological activities and molecular docking studies.
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- Chemical Biology & Drug Design, 2023, v. 102, n. 6, p. 1458, doi. 10.1111/cbdd.14336
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- Article
Design, Synthesis, and Investigation of Anticancer and Antioxidant Potential of Novel Indole‐Based Melatonin Analogues in Breast Cancer.
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- ChemistrySelect, 2024, v. 9, n. 25, p. 1, doi. 10.1002/slct.202400817
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- Article
Novel Indole-Based Hydrazones as Potent Inhibitors of the α-class Carbonic Anhydrase from Pathogenic Bacterium Vibrio cholerae.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 9, p. 3131, doi. 10.3390/ijms21093131
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- Article
Indole-Based Hydrazones Containing A Sulfonamide Moiety as Selective Inhibitors of Tumor-Associated Human Carbonic Anhydrase Isoforms IX and XII.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 9, p. 2354, doi. 10.3390/ijms20092354
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Thiosemicarbazide-Substituted Coumarins as Selective Inhibitors of the Tumor Associated Human Carbonic Anhydrases IX and XII.
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- Molecules, 2022, v. 27, n. 14, p. N.PAG, doi. 10.3390/molecules27144610
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Five- and Six-Membered Nitrogen-Containing Compounds as Selective Carbonic Anhydrase Activators.
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- Molecules, 2017, v. 22, n. 12, p. 2178, doi. 10.3390/molecules22122178
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- Article
Computer-aided Drug Design on Glioblastoma Multiforme: Investigating Possible Inhibitors Against Factor H.
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- Bezmialem Science, 2022, v. 10, p. S30
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- Article
İnsan Metilentetrahidrofolat Redüktaz Enziminin Kristal Yapısı İçin Bir Model.
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- Journal of Harran University Medical Faculty / Harran Üniversitesi Tıp Fakültesi Dergisi, 2015, v. 12, n. 1, p. 23
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Synthesis, cytotoxic activities and molecular modeling studies of some 2-aminonaphtho[2,3-d][1,3]thiazole-4,9-dione derivatives.
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- Organic Communications, 2020, v. 13, n. 4, p. 184, doi. 10.25135/acg.oc.91.20.11.1913
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Design and synthesis of novel peptidomimetics for cancer immunotherapy.
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- Organic Communications, 2020, v. 13, n. 3, p. 89, doi. 10.25135/acg.oc.86.20.09.1802
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- Article
Evaluation of new 2-hydroxy-N-(4-oxo-2-substituted phenyl-1,3- thiazolidin-3-yl)-2-phenylacetamide derivatives as potential antimycobacterial agents.
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- Organic Communications, 2020, v. 13, n. 2, p. 33, doi. 10.25135/acg.oc.78.20.05.1655
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- Article
New 1H‐indole‐2,3‐dione 3‐thiosemicarbazones with 3‐sulfamoylphenyl moiety as selective carbonic anhydrase inhibitors.
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- Archiv der Pharmazie, 2022, v. 355, n. 8, p. 1, doi. 10.1002/ardp.202200023
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- Article
Synthesis of new 1,2,4‐triazole–(thio)semicarbazide hybrid molecules: Their tyrosinase inhibitor activities and molecular docking analysis.
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- Archiv der Pharmazie, 2021, v. 354, n. 8, p. 1, doi. 10.1002/ardp.202100058
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rac‐ and meso‐Cyclohexanoids: Their α‐, β‐glycosidases, antibacterial, antifungal activities, and molecular docking studies.
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- Archiv der Pharmazie, 2020, v. 353, n. 3, p. 1, doi. 10.1002/ardp.201900267
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- Article
Design and synthesis of new heterocyclic compounds containing 5-[(1H-1,2,4-triazol-1-yl)methyl]-3H-1,2,4-triazole-3-thione structure as potent hEGFR inhibitors.
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- Journal of Biomolecular Structure & Dynamics, 2023, v. 41, n. 22, p. 12753, doi. 10.1080/07391102.2023.2167113
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Synthesis, anti‐TB activities, and molecular docking studies of 4‐(1,2,3‐triazoyl)arylmethanone derivatives.
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- Journal of Biochemical & Molecular Toxicology, 2022, v. 36, n. 4, p. 1, doi. 10.1002/jbt.22998
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- Article
Antiviral Properties of 5‑Sulfamoyl‑1H‑Indole-Linked Spirothiazolidinone Derivatives: A Study on Human Parainfluenza Virus-2.
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- Journal of Research in Pharmacy, 2024, v. 28, n. 1, p. 213, doi. 10.29228/jrp.689
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Molecular modelling studies to suggest novel scaffolds against SARS-CoV-2 target enzymes.
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- Journal of Research in Pharmacy, 2021, v. 25, n. 6, p. 1010, doi. 10.29228/jrp.96
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- Article
YÖRESEL TAVIR BAĞLAMINDA SAHİH TİLAVET KRİTERLERİ.
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- Review of the Faculty of Divinity of Amasya University, 2018, n. 11, p. 9, doi. 10.18498/amauifd.503733
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- Article
Azole-Based Compounds That Are Active against Candida Biofilm: In Vitro , In Vivo and In Silico Studies.
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- Antibiotics (2079-6382), 2022, v. 11, n. 10, p. N.PAG, doi. 10.3390/antibiotics11101375
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- Article
Carbonic Anhydrase Inhibitors Targeting Metabolism and Tumor Microenvironment.
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- Metabolites (2218-1989), 2020, v. 10, n. 10, p. 412, doi. 10.3390/metabo10100412
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- Article