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For: Osmaniye D, Türkeş C, Demir Y, Özkay Y, Beydemir Ş, Kaplancıklı ZA. Design, synthesis, and biological activity of novel dithiocarbamate-methylsulfonyl hybrids as carbonic anhydrase inhibitors. Arch Pharm (Weinheim) 2022;:e2200132. [PMID: 35502846 DOI: 10.1002/ardp.202200132] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 11.0] [Reference Citation Analysis]
Number Citing Articles
1 Yakan H, Muğlu H, Türkeş C, Demir Y, Erdoğan M, Çavuş MS, Beydemir Ş. A novel series of thiosemicarbazone hybrid scaffolds: Design, Synthesis, DFT studies, metabolic enzyme inhibition properties, and molecular docking calculations. Journal of Molecular Structure 2023. [DOI: 10.1016/j.molstruc.2023.135077] [Reference Citation Analysis]
2 Altıntop MD, Demir Y, Türkeş C, Öztürk RB, Cantürk Z, Beydemir Ş, Özdemir A. A new series of hydrazones as small-molecule aldose reductase inhibitors. Arch Pharm (Weinheim) 2023;:e2200570. [PMID: 36603162 DOI: 10.1002/ardp.202200570] [Reference Citation Analysis]
3 Kakakhan C, Türkeş C, Güleç Ö, Demir Y, Arslan M, Özkemahlı G, Beydemir Ş. Exploration of 1,2,3-triazole linked benzenesulfonamide derivatives as isoform selective inhibitors of human carbonic anhydrase. Bioorg Med Chem 2023;77:117111. [PMID: 36463726 DOI: 10.1016/j.bmc.2022.117111] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Demir Y, Türkeş C, Küfrevioğlu Öİ, Beydemir Ş. Molecular Docking Studies and the Effect of Fluorophenylthiourea Derivatives on Glutathione-Dependent Enzymes. Chem Biodivers 2023;20:e202200656. [PMID: 36538730 DOI: 10.1002/cbdv.202200656] [Reference Citation Analysis]
5 Demir Y, Türkeş C, Çavuş MS, Erdoğan M, Muğlu H, Yakan H, Beydemir Ş. Enzyme inhibition, molecular docking, and density functional theory studies of new thiosemicarbazones incorporating the 4-hydroxy-3,5-dimethoxy benzaldehyde motif. Arch Pharm (Weinheim) 2022;:e2200554. [PMID: 36575148 DOI: 10.1002/ardp.202200554] [Reference Citation Analysis]
6 Türkeş C, Demir Y, Beydemir Ş. In Vitro Inhibitory Activity and Molecular Docking Study of Selected Natural Phenolic Compounds as AR and SDH Inhibitors**. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202204050] [Reference Citation Analysis]
7 Tawfik HO, Belal A, Abourehab MAS, Angeli A, Bonardi A, Supuran CT, El-Hamamsy MH. Dependence on linkers' flexibility designed for benzenesulfonamides targeting discovery of novel hCA IX inhibitors as potent anticancer agents. J Enzyme Inhib Med Chem 2022;37:2765-85. [PMID: 36210545 DOI: 10.1080/14756366.2022.2130285] [Reference Citation Analysis]
8 Yararli K, Ozer EB, Bayindir S, Caglayan C, Turkes C, Beydemir S. The synthesis, biological evaluation and in silico studies of asymmetric 3,5-diaryl-rhodanines as novel inhibitors of human carbonic anhydrase isoenzymes. Journal of Molecular Structure 2022. [DOI: 10.1016/j.molstruc.2022.134783] [Reference Citation Analysis]
9 Tapera M, Kekeçmuhammed H, Tüzün B, Sarıpınar E, Koçyiğit ÜM, Yıldırım E, Doğan M, Zorlu Y. Synthesis, carbonic anhydrase inhibitory activity, anticancer activity and molecular docking studies of new imidazolyl hydrazone derivatives. Journal of Molecular Structure 2022;1269:133816. [DOI: 10.1016/j.molstruc.2022.133816] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Mohammadi-liri A, Parsa-khankandi H, Dehnoee A, Mojtabavi S, Faramarzi MA, Delnavazi M. α-Glucosidase inhibitors from the aerial part of Thymus fedtschenkoi: isolation, kinetic and molecular docking study. Chem Pap . [DOI: 10.1007/s11696-022-02511-7] [Reference Citation Analysis]
11 Demir Y, Tokalı FS, Kalay E, Türkeş C, Tokalı P, Aslan ON, Şendil K, Beydemir Ş. Synthesis and characterization of novel acyl hydrazones derived from vanillin as potential aldose reductase inhibitors. Mol Divers. [DOI: 10.1007/s11030-022-10526-1] [Reference Citation Analysis]
12 Özaslan MS, Sağlamtaş R, Demir Y, Genç Y, Saraçoğlu İ, Gülçin İ. Isolation of Some Phenolic Compounds from Plantago subulata L. and Determination of Their Antidiabetic, Anticholinesterase, Antiepileptic and Antioxidant Activity. Chem Biodivers 2022;:e202200280. [PMID: 35796520 DOI: 10.1002/cbdv.202200280] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Korkmaz IN, Türkeş C, Demir Y, Özdemir H, Beydemir Ş. Methyl benzoate derivatives: in vitro Paraoxonase 1 inhibition and in silico studies. J Biochem Mol Toxicol 2022;:e23152. [PMID: 35708184 DOI: 10.1002/jbt.23152] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]