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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

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
Sercan Askin, Hakan Tahtacı, Cüneyt Türkeş, et al.
Bioorganic Chemistry (2021) Vol. 113, pp. 105009-105009
Closed Access | Times Cited: 92

Showing 1-25 of 92 citing articles:

Cytotoxic effect, enzyme inhibition, and in silico studies of some novel N-substituted sulfonyl amides incorporating 1,3,4-oxadiazol structural motif
Özcan Güleç, Cüneyt Türkeş, Mustafa Arslan, et al.
Molecular Diversity (2022) Vol. 26, Iss. 5, pp. 2825-2845
Open Access | Times Cited: 79
Exploration of 1,2,3-triazole linked benzenesulfonamide derivatives as isoform selective inhibitors of human carbonic anhydrase
Chnar Kakakhan, Cüneyt Türkeş, Özcan Güleç, et al.
Bioorganic & Medicinal Chemistry (2022) Vol. 77, pp. 117111-117111
Closed Access | Times Cited: 75
Design, synthesis, biological evaluation and molecular docking studies of novel 1H-1,2,3-Triazole derivatives as potent inhibitors of carbonic anhydrase, acetylcholinesterase and aldose reductase
Derya Aktaş Anıl, Busra Ozturk Aydin, Yeliz Demir, et al.
Journal of Molecular Structure (2022) Vol. 1257, pp. 132613-132613
Closed Access | Times Cited: 72
Design, synthesis, and biological activity of novel dithiocarbamate‐methylsulfonyl hybrids as carbonic anhydrase inhibitors
Derya Osmani̇ye, Cüneyt Türkeş, Yeliz Demir, et al.
Archiv der Pharmazie (2022) Vol. 355, Iss. 8
Closed Access | Times Cited: 65
Discovery of novel benzenesulfonamides incorporating 1,2,3-triazole scaffold as carbonic anhydrase I, II, IX, and XII inhibitors
Aida Buza, Cüneyt Türkeş, Mustafa Arslan, et al.
International Journal of Biological Macromolecules (2023) Vol. 239, pp. 124232-124232
Closed Access | Times Cited: 60
Novel beta-lactam substituted benzenesulfonamides: in vitro enzyme inhibition, cytotoxic activity and in silico interactions
Özcan Güleç, Cüneyt Türkeş, Mustafa Arslan, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 12, pp. 6359-6377
Closed Access | Times Cited: 44
Molecular docking and inhibition studies of vulpinic, carnosic and usnic acids on polyol pathway enzymes
Yeliz Demir, Hamid Ceylan, Cüneyt Türkeş, et al.
Journal of Biomolecular Structure and Dynamics (2021) Vol. 40, Iss. 22, pp. 12008-12021
Closed Access | Times Cited: 77
Novel metabolic enzyme inhibitors designed through the molecular hybridization of thiazole and pyrazoline scaffolds
Belgin Sever, Cüneyt Türkeş, Mehlika Dilek Altıntop, et al.
Archiv der Pharmazie (2021) Vol. 354, Iss. 12
Closed Access | Times Cited: 70
Transition‐Metal Complexes of Bidentate Schiff‐Base Ligands: In Vitro and In Silico Evaluation as Non‐Classical Carbonic Anhydrase and Potential Acetylcholinesterase Inhibitors
Ümit Yaşar, İlyas Gönül, Cüneyt Türkeş, et al.
ChemistrySelect (2021) Vol. 6, Iss. 29, pp. 7278-7284
Closed Access | Times Cited: 68
Biological effects of bis-hydrazone compounds bearing isovanillin moiety on the aldose reductase
Gönül Yapar, Hatice Esra Duran, Nebih Lolak, et al.
Bioorganic Chemistry (2021) Vol. 117, pp. 105473-105473
Closed Access | Times Cited: 59
An Overview of the Biological Evaluation of Selected Nitrogen-Containing Heterocycle Medicinal Chemistry Compounds
Oluwakemi Ebenezer, Maryam Amra. Jordaan, Gea Carena, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 15, pp. 8117-8117
Open Access | Times Cited: 51
Novel bis-ureido-substituted sulfaguanidines and sulfisoxazoles as carbonic anhydrase and acetylcholinesterase inhibitors
Nebih Lolak, Süleyman Akocak, Mustafa Durgun, et al.
Molecular Diversity (2022) Vol. 27, Iss. 4, pp. 1735-1749
Closed Access | Times Cited: 47
Synthesis and characterization of novel acyl hydrazones derived from vanillin as potential aldose reductase inhibitors
Yeliz Demir, Feyzi Sinan Tokalı, Erbay Kalay, et al.
Molecular Diversity (2022) Vol. 27, Iss. 4, pp. 1713-1733
Closed Access | Times Cited: 46
Isolation of Some Phenolic Compounds from Plantago subulata L. and Determination of Their Antidiabetic, Anticholinesterase, Antiepileptic and Antioxidant Activity
Muhammet Serhat Özaslan, Rüya Sağlamtaş, Yeliz Demir, et al.
Chemistry & Biodiversity (2022) Vol. 19, Iss. 8
Closed Access | Times Cited: 45
Synthesis, carbonic anhydrase inhibitory activity, anticancer activity and molecular docking studies of new imidazolyl hydrazone derivatives
Michael Tapera, Hüseyin Kekeçmuhammed, Burak Tüzün, et al.
Journal of Molecular Structure (2022) Vol. 1269, pp. 133816-133816
Closed Access | Times Cited: 42
Novel acetic acid derivatives containing quinazolin‐4(3H)‐one ring: Synthesis, in vitro, and in silico evaluation of potent aldose reductase inhibitors
Feyzi Sinan Tokalı, Yeliz Demir, Cüneyt Türkeş, et al.
Drug Development Research (2023) Vol. 84, Iss. 2, pp. 275-295
Closed Access | Times Cited: 33
A novel series of thiosemicarbazone hybrid scaffolds: Design, synthesis, DFT studies, metabolic enzyme inhibition properties, and molecular docking calculations
Hasan Yakan, Halit Muğlu, Cüneyt Türkeş, et al.
Journal of Molecular Structure (2023) Vol. 1280, pp. 135077-135077
Closed Access | Times Cited: 27
Exploration of Some Bis‐Sulfide and Bis‐Sulfone Derivatives as Non‐Classical Aldose Reductase İnhibitors
Cüneyt Türkeş, Yeliz Demir, Abdullah Biçer, et al.
ChemistrySelect (2023) Vol. 8, Iss. 5
Closed Access | Times Cited: 19
Structural characterization and biological evaluation of uracil-appended benzylic amines as acetylcholinesterase and carbonic anhydrase I and II inhibitors
Zafer Bulut, Nurgül Abul, Ayşe Halıç Poslu, et al.
Journal of Molecular Structure (2023) Vol. 1280, pp. 135047-135047
Closed Access | Times Cited: 19
Discovery of Potential Rosin-Based Triazole Antifungal Candidates to Control Valsa mali for Sustainable Crop Protection
Renle Xu, Han Xu, Yuhang Lou, et al.
Journal of Agricultural and Food Chemistry (2024) Vol. 72, Iss. 9, pp. 4630-4638
Closed Access | Times Cited: 7
Design, synthesis and in silico insights of novel 1,2,3-triazole benzenesulfonamide derivatives as potential carbonic anhydrase IX and XII inhibitors with promising anticancer activity
Marwa M. Abdelhakeem, Martha M. Morcoss, Dina Hanna, et al.
Bioorganic Chemistry (2024) Vol. 144, pp. 107154-107154
Closed Access | Times Cited: 6
Identification of a new class of potent aldose reductase inhibitors: Design, microwave-assisted synthesis, in vitro and in silico evaluation of 2-pyrazolines
Belgin Sever, Mehlika Dilek Altıntop, Yeliz Demir, et al.
Chemico-Biological Interactions (2021) Vol. 345, pp. 109576-109576
Closed Access | Times Cited: 49
Synthesis, biological evaluation, and in silico study of novel library sulfonates containing quinazolin‐4(3H)‐one derivatives as potential aldose reductase inhibitors
Feyzi Sinan Tokalı, Yeliz Demir, İbrahim Hakkı Demircioğlu, et al.
Drug Development Research (2021)
Closed Access | Times Cited: 48
Infection Medications: Assessment In‐Vitro Glutathione S‐Transferase Inhibition and Molecular Docking Study
Cüneyt Türkeş, Yeliz Demir, Şükrü Beydemir
ChemistrySelect (2021) Vol. 6, Iss. 43, pp. 11915-11924
Closed Access | Times Cited: 48
Calcium Channel Blockers: The Effect of Glutathione S‐Transferase Enzyme Activity and Molecular Docking Studies
Cüneyt Türkeş, Arzu Öztürk Kesebir, Yeliz Demir, et al.
ChemistrySelect (2021) Vol. 6, Iss. 40, pp. 11137-11143
Closed Access | Times Cited: 39
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