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For: Türkeş C, Akocak S, Işık M, Lolak N, Taslimi P, Durgun M, Gülçin İ, Budak Y, Beydemir Ş. Novel inhibitors with sulfamethazine backbone: synthesis and biological study of multi-target cholinesterases and α-glucosidase inhibitors. J Biomol Struct Dyn 2022;40:8752-64. [PMID: 33950796 DOI: 10.1080/07391102.2021.1916599] [Cited by in Crossref: 23] [Cited by in F6Publishing: 23] [Article Influence: 11.5] [Reference Citation Analysis]
Number Citing Articles
1 Türkeş C, Demir Y, Biçer A, Cin GT, Gültekin MS, Beydemir Ş. Exploration of Some Bis‐Sulfide and Bis‐Sulfone Derivatives as Non‐Classical Aldose Reductase İnhibitors. ChemistrySelect 2023;8. [DOI: 10.1002/slct.202204350] [Reference Citation Analysis]
2 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]
3 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]
4 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]
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 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]
8 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]
9 Al-khayri JM, Yüksel AK, Yüksel M, Işık M, Dikici E. Phenolic Profile and Antioxidant, Anticholinergic, and Antibacterial Properties of Corn Tassel. Plants 2022;11:1899. [DOI: 10.3390/plants11151899] [Reference Citation Analysis]
10 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]
11 Işık M. Cholinesterases and Their Inhibitors. Hydrolases 2022. [DOI: 10.5772/intechopen.102585] [Reference Citation Analysis]
12 Tekeli Y, Lolak N, Sonmez GD, Tekeli T, Akocak S. Antibacterial, Antioxidant and DNA Cleavage Activity Evaluation of Substituted Phenylureido Sulfaguanidine and Sulfamethazine Derivatives. Pharm Chem J. [DOI: 10.1007/s11094-022-02654-7] [Reference Citation Analysis]
13 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]
14 Korkmaz A, Rhyman L, Ramasami P. Synthesis, characterization, DFT and molecular docking studies of acetone O-((2,5-dichlorophenyl)sulfonyl) oxime. Physical Sciences Reviews 2022;0. [DOI: 10.1515/psr-2021-0230] [Reference Citation Analysis]
15 Mehmood R, Sadiq A, Alsantali RI, Mughal EU, Alsharif MA, Naeem N, Javid A, Al-Rooqi MM, Chaudhry GE, Ahmed SA. Synthesis and Evaluation of 1,3,5-Triaryl-2-Pyrazoline Derivatives as Potent Dual Inhibitors of Urease and α-Glucosidase Together with Their Cytotoxic, Molecular Modeling and Drug-Likeness Studies. ACS Omega 2022;7:3775-95. [PMID: 35128286 DOI: 10.1021/acsomega.1c06694] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
16 Kavaz Yüksel A, Dikici E, Yüksel M, Işik M. Abelmoschus esculentus (Bamya Çiçeği) Çiçeğinin Fitokimyasal Profili, Antioksidan, Antikolinerjik ve Antibakteriyel Özellikleri. Kahramanmaraş Sütçü İmam Üniversitesi Tarım ve Doğa Dergisi 2021. [DOI: 10.18016/ksutarimdoga.vi.976717] [Reference Citation Analysis]
17 Yapar G, Esra Duran H, Lolak N, Akocak S, Türkeş C, Durgun M, Işık M, Beydemir Ş. Biological effects of bis-hydrazone compounds bearing isovanillin moiety on the aldose reductase. Bioorg Chem 2021;117:105473. [PMID: 34768205 DOI: 10.1016/j.bioorg.2021.105473] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
18 Türkeş C, Kesebir AÖ, Demir Y, Küfrevioğlu Öİ, Beydemir Ş. Calcium Channel Blockers: The Effect of Glutathione S‐Transferase Enzyme Activity and Molecular Docking Studies. ChemistrySelect 2021;6:11137-43. [DOI: 10.1002/slct.202103100] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 6.0] [Reference Citation Analysis]
19 Tokalı FS, Demir Y, Demircioğlu İH, Türkeş C, Kalay E, Şendil K, Beydemir Ş. Synthesis, biological evaluation, and in silico study of novel library sulfonates containing quinazolin-4(3H)-one derivatives as potential aldose reductase inhibitors. Drug Dev Res 2021. [PMID: 34585414 DOI: 10.1002/ddr.21887] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 7.5] [Reference Citation Analysis]
20 Demir Y, Ceylan H, Türkeş C, Beydemir Ş. Molecular docking and inhibition studies of vulpinic, carnosic and usnic acids on polyol pathway enzymes. J Biomol Struct Dyn 2022;40:12008-21. [PMID: 34424822 DOI: 10.1080/07391102.2021.1967195] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 8.5] [Reference Citation Analysis]
21 Pachón-Angona I, Maj M, Wnorowski A, Martin H, Jóźwiak K, Ismaili L. Synthesis of new Hantzsch adducts showing Ca2+ channel blockade capacity, cholinesterase inhibition and antioxidant power. Future Med Chem 2021;13:1717-29. [PMID: 34402661 DOI: 10.4155/fmc-2021-0176] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
22 Cetin G, Tras B, Uney K. The Effects of P‐glycoprotein Modulators on the Transition of Levofloxacin to Rat Brain, Testicle, and Plasma: In Vivo and In Silico Studies. ChemistrySelect 2021;6:7476-81. [DOI: 10.1002/slct.202102122] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
23 Kavaz Yüksel A, Dikici E, Yüksel M, Işık M, Tozoğlu F, Köksal E. Phytochemical, phenolic profile, antioxidant, anticholinergic and antibacterial properties of Epilobium angustifolium (Onagraceae). Food Measure 2021;15:4858-67. [DOI: 10.1007/s11694-021-01050-1] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
24 Askin S, Tahtaci H, Türkeş C, Demir Y, Ece A, Akalın Çiftçi G, Beydemir Ş. Design, synthesis, characterization, in vitro and in silico evaluation of novel imidazo[2,1-b][1,3,4]thiadiazoles as highly potent acetylcholinesterase and non-classical carbonic anhydrase inhibitors. Bioorg Chem 2021;113:105009. [PMID: 34052739 DOI: 10.1016/j.bioorg.2021.105009] [Cited by in Crossref: 43] [Cited by in F6Publishing: 44] [Article Influence: 21.5] [Reference Citation Analysis]