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For: 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]
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 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]
3 Bulut Z, Abul N, Poslu AH, Gülcin İ, Ece A, Erçağ E, Koz Ö, Koz G. Structural Characterization and Biological Evaluation of Uracil-Appended Benzylic Amines as Acetylcholinesterase and Carbonic Anhydrase I and II Inhibitors. Journal of Molecular Structure 2023. [DOI: 10.1016/j.molstruc.2023.135047] [Reference Citation Analysis]
4 Saha N, Wanjari PJ, Dubey G, Mahawar N, Bharatam PV. Metal-free synthesis of imidazoles and 2-aminoimidazoles. Journal of Molecular Structure 2023;1272:134092. [DOI: 10.1016/j.molstruc.2022.134092] [Reference Citation Analysis]
5 Gültekin E, Bekircan O, Kara Y, Güler Hİ, Soylu MS, Kolaylı S. 1,3,4-Thiadiazole and 1,2,4-triazole-5-thione derivatives bearing 2-pentyl-5-phenyl-2,4-dihydro-3H-1,2,4-triazole-3-one ring: Synthesis, molecular docking, urease inhibition, and crystal structure. Arch Pharm (Weinheim) 2023;356:e2200355. [PMID: 36316247 DOI: 10.1002/ardp.202200355] [Reference Citation Analysis]
6 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]
7 Ozcan I, Akkoc S, Alici H, Capanlar S, Sahin O, Tahtaci H. Novel Thioether-Bridged 2,6-Disubstituted and 2,5,6-Trisubstituted Imidazothiadiazole Analogues: Synthesis, Antiproliferative Activity, ADME, and Molecular Docking Studies. Chem Biodivers 2023;20:e202200884. [PMID: 36445849 DOI: 10.1002/cbdv.202200884] [Reference Citation Analysis]
8 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]
9 Demirci Ö, Tezcan B, Demir Y, Taskin-tok T, Gök Y, Aktaş A, Güzel B, Gülçin İ. Acetylphenyl-substituted imidazolium salts: synthesis, characterization, in silico studies and inhibitory properties against some metabolic enzymes. Mol Divers 2022. [DOI: 10.1007/s11030-022-10578-3] [Reference Citation Analysis]
10 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]
11 Hamide M, Gök Y, Demir Y, Sevinçek R, Taskin-Tok T, Tezcan B, Aktaş A, Gülçin İ, Aygün M, Güzel B. Benzimidazolium Salts Containing Trifluoromethoxybenzyl: Synthesis, Characterization, Crystal Structure, Molecular Docking Studies and Enzymes Inhibitory Properties. Chem Biodivers 2022;19:e202200257. [PMID: 36260838 DOI: 10.1002/cbdv.202200257] [Reference Citation Analysis]
12 Çalışkan B, Demir Y, Türkeş C. Ophthalmic drugs: in vitro paraoxonase 1 inhibition and molecular docking studies. Biotechnol Appl Biochem 2022;69:2273-83. [PMID: 34786760 DOI: 10.1002/bab.2284] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 9.0] [Reference Citation Analysis]
13 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]
14 Rashdan HRM, Abdelmonsef AH. Towards Covid-19 TMPRSS2 enzyme inhibitors and antimicrobial agents: Synthesis, antimicrobial potency, molecular docking, and drug-likeness prediction of thiadiazole-triazole hybrids. J Mol Struct 2022;1268:133659. [PMID: 35818577 DOI: 10.1016/j.molstruc.2022.133659] [Reference Citation Analysis]
15 Chortani S, Hajlaoui A, Jlizi S, Harrath AH, Ben Jannet H, Romdhane A. Access to new phosphonate- and imidazolidine-benzopyrimidinone derivatives as antityrosinase and anti-acetylcholinesterase agents: Design, synthesis and molecular docking. Journal of Molecular Structure 2022;1268:133693. [DOI: 10.1016/j.molstruc.2022.133693] [Reference Citation Analysis]
16 Demirci Ö, Tezcan B, Demir Y, Taskin-tok T, Gök Y, Aktaş A, Güzel B, Gülçin İ. Acetylphenyl-Substituted Imidazolium Salts: Synthesis, Characterization, in silico Studies and Inhibitory Properties against Some Metabolic Enzymes.. [DOI: 10.21203/rs.3.rs-2161155/v1] [Reference Citation Analysis]
17 El-sofany WI, Flefel EM, Darwesh OM, El-shahat M. Boosting the antimicrobial performance based on new fused spirothiazolidine framework analogs. J IRAN CHEM SOC 2022;19:4223-4236. [DOI: 10.1007/s13738-022-02595-8] [Reference Citation Analysis]
18 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]
19 Rasool A, Batool Z, Khan M, Halim SA, Shafiq Z, Temirak A, Salem MA, Ali TE, Khan A, Al-Harrasi A. Bis-pharmacophore of cinnamaldehyde-clubbed thiosemicarbazones as potent carbonic anhydrase-II inhibitors. Sci Rep 2022;12:16095. [PMID: 36167735 DOI: 10.1038/s41598-022-19975-y] [Reference Citation Analysis]
20 Yiğit M, Demir Y, Barut Celepci D, Taskin-Tok T, Arınç A, Yiğit B, Aygün M, Özdemir İ, Gülçin İ. Phthalimide-tethered imidazolium salts: Synthesis, characterization, enzyme inhibitory properties, and in silico studies. Arch Pharm (Weinheim) 2022;:e2200348. [PMID: 36153848 DOI: 10.1002/ardp.202200348] [Reference Citation Analysis]
21 Lolak N, Akocak S, Durgun M, Duran HE, Necip A, Türkeş C, Işık M, Beydemir Ş. Novel bis-ureido-substituted sulfaguanidines and sulfisoxazoles as carbonic anhydrase and acetylcholinesterase inhibitors. Mol Divers 2022. [PMID: 36136229 DOI: 10.1007/s11030-022-10527-0] [Reference Citation Analysis]
22 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]
23 Muhammad Ghali U, Teralı K, Dalmızrak Ö, Özer N. Rethinking common solvents in butyrylcholinesterase activity assays. Inorganic Chemistry Communications 2022;143:109796. [DOI: 10.1016/j.inoche.2022.109796] [Reference Citation Analysis]
24 Durmaz Ş, Evren AE, Sağlık BN, Yurttaş L, Tay NF. Synthesis, anticholinesterase activity, molecular docking, and molecular dynamic simulation studies of 1,3,4-oxadiazole derivatives. Arch Pharm (Weinheim) 2022;:e2200294. [PMID: 35972839 DOI: 10.1002/ardp.202200294] [Reference Citation Analysis]
25 Korkmaz IN, Türkeş C, Demir Y, Öztekin A, Özdemir H, Beydemir Ş. Biological evaluation and in silico study of benzohydrazide derivatives as paraoxonase 1 inhibitors. J Biochem Mol Toxicol 2022;:e23180. [PMID: 35916346 DOI: 10.1002/jbt.23180] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
26 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]
27 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]
28 Akdağ M, Özçelik AB, Demir Y, Beydemir Ş. Design, synthesis, and aldose reductase inhibitory effect of some novel carboxylic acid derivatives bearing 2-substituted-6-aryloxo-pyridazinone moiety. Journal of Molecular Structure 2022;1258:132675. [DOI: 10.1016/j.molstruc.2022.132675] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
29 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]
30 Güleç Ö, Türkeş C, Arslan M, Demir Y, Yeni Y, Hacımüftüoğlu A, Ereminsoy E, Küfrevioğlu Öİ, Beydemir Ş. Cytotoxic effect, enzyme inhibition, and in silico studies of some novel N-substituted sulfonyl amides incorporating 1,3,4-oxadiazol structural motif. Mol Divers 2022. [PMID: 35397086 DOI: 10.1007/s11030-022-10422-8] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
31 Yushyn I, Holota S, Lesyk R. 2,2-Dichloro-N-[5-[2-[3-(4-methoxyphenyl)-5-phenyl-3,4-dihydro-2H-pyrazol-2-yl]-2-oxoethyl]sulfanyl-1,3,4-thiadiazol-2-yl]acetamide. Molbank 2022;2022:M1328. [DOI: 10.3390/m1328] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
32 Shehadi IA, Abdelrahman MT, Abdelraof M, Rashdan HRM. Solvent-Free Synthesis, In Vitro and In Silico Studies of Novel Potential 1,3,4-Thiadiazole-Based Molecules against Microbial Pathogens. Molecules 2022;27:342. [PMID: 35056655 DOI: 10.3390/molecules27020342] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
33 Türkeş C, Demir Y, Beydemir Ş. Infection Medications: Assessment In‐Vitro Glutathione S‐Transferase Inhibition and Molecular Docking Study. ChemistrySelect 2021;6:11915-24. [DOI: 10.1002/slct.202103197] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 6.0] [Reference Citation Analysis]
34 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]
35 Li XY, Wang DP, Li S, Xue WH, Qian XH, Liu KL, Li YH, Lin QQ, Dong G, Meng FH, Jian LY. Discovery of N-(1,3,4-thiadiazol-2-yl)benzamide derivatives containing a 6,7-methoxyquinoline structure as novel EGFR/HER-2 dual-target inhibitors against cancer growth and angiogenesis. Bioorg Chem 2021;119:105469. [PMID: 34915285 DOI: 10.1016/j.bioorg.2021.105469] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
36 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]
37 Erdogan M, Kiymaz K, Tahtaci H, Uysal S. Synthesis and characterization of the Co(II) and Ni(II) complexes of 1,3,4-thiadiazole-derived ketones and secondary alcohols: thermal and magnetic properties. Journal of Coordination Chemistry 2021;74:2508-33. [DOI: 10.1080/00958972.2021.1992401] [Reference Citation Analysis]
38 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]
39 Sever B, Türkeş C, Altıntop MD, Demir Y, Akalın Çiftçi G, Beydemir Ş. Novel metabolic enzyme inhibitors designed through the molecular hybridization of thiazole and pyrazoline scaffolds. Arch Pharm (Weinheim) 2021;:e2100294. [PMID: 34569655 DOI: 10.1002/ardp.202100294] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 7.0] [Reference Citation Analysis]
40 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]
41 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]
42 Yaşar Ü, Gönül İ, Türkeş C, Demir Y, Beydemir Ş. Transition‐Metal Complexes of Bidentate Schiff‐Base Ligands: In Vitro and In Silico Evaluation as Non‐Classical Carbonic Anhydrase and Potential Acetylcholinesterase Inhibitors. ChemistrySelect 2021;6:7278-84. [DOI: 10.1002/slct.202102082] [Cited by in Crossref: 25] [Cited by in F6Publishing: 25] [Article Influence: 12.5] [Reference Citation Analysis]
43 Nural Y, Ozdemir S, Yalcin MS, Demir B, Atabey H, Ece A, Seferoglu Z. Synthesis, Biological Evaluation, Molecular Docking, and Acid Dissociation Constant of New Bis‐1,2,3‐triazole Compounds. ChemistrySelect 2021;6:6994-7001. [DOI: 10.1002/slct.202101148] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
44 Sever B, Altıntop MD, Demir Y, Yılmaz N, Akalın Çiftçi G, Beydemir Ş, Özdemir A. Identification of a new class of potent aldose reductase inhibitors: Design, microwave-assisted synthesis, in vitro and in silico evaluation of 2-pyrazolines. Chem Biol Interact 2021;345:109576. [PMID: 34252406 DOI: 10.1016/j.cbi.2021.109576] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 6.0] [Reference Citation Analysis]