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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:

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

Showing 1-25 of 47 citing articles:

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
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: 62
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: 46
Bioactivity, cytotoxicity, and molecular modeling studies of novel sulfonamides as dual inhibitors of carbonic anhydrases and acetylcholinesterase
Özcan Güleç, Cüneyt Türkeş, Mustafa Arslan, et al.
Journal of Molecular Liquids (2024) Vol. 410, pp. 125558-125558
Closed Access | Times Cited: 17
Enzyme inhibition, molecular docking, and density functional theory studies of new thiosemicarbazones incorporating the 4‐hydroxy‐3,5‐dimethoxy benzaldehyde motif
Yeliz Demir, Cüneyt Türkeş, M. Serdar Çavuş, et al.
Archiv der Pharmazie (2022) Vol. 356, Iss. 4
Closed Access | Times Cited: 36
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: 34
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
Dynamics of small molecule-enzyme interactions: Novel benzenesulfonamides as multi-target agents endowed with inhibitory effects against some metabolic enzymes
Özcan Güleç, Cüneyt Türkeş, Mustafa Arslan, et al.
Archives of Biochemistry and Biophysics (2024) Vol. 759, pp. 110099-110099
Closed Access | Times Cited: 9
Antioxidant and anti-inflammatory activity through inhibition of NF-κB and sEH of some citrus peel and phytoconstituent characteristics
Yesi Desmiaty, Ni Made Dwi Sandhiutami, Esti Mulatsari, et al.
Saudi Pharmaceutical Journal (2024) Vol. 32, Iss. 2, pp. 101959-101959
Open Access | Times Cited: 5
Exploring the potency of diazo‐coumarin containing hybrid molecules: Selective inhibition of tumor‐associated carbonic anhydrase isoforms IX and XII
Gönül Yapar, Nebih Lolak, Alessandro Bonardi, et al.
ChemMedChem (2024) Vol. 19, Iss. 4
Closed Access | Times Cited: 4
New N -(1,3,4-thiadiazole-2-yl)acetamide derivatives as human carbonic anhydrase I and II and acetylcholinesterase inhibitors
Sam Dawbaa, Cüneyt Türkeş, Demokrat Nuha, et al.
Journal of Biomolecular Structure and Dynamics (2024), pp. 1-19
Closed Access | Times Cited: 4
In Vitro Inhibitory Activity and Molecular Docking Study of Selected Natural Phenolic Compounds as AR and SDH Inhibitors**
Cüneyt Türkeş, Yeliz Demir, Şükrü Beydemir
ChemistrySelect (2022) Vol. 7, Iss. 48
Open Access | Times Cited: 23
A new series of hydrazones as small‐molecule aldose reductase inhibitors
Mehlika Dilek Altıntop, Yeliz Demir, Cüneyt Türkeş, et al.
Archiv der Pharmazie (2023) Vol. 356, Iss. 4
Closed Access | Times Cited: 13
Benzimidazole-derived carbohydrazones as dual monoamine oxidases and acetylcholinesterase inhibitors: design, synthesis, and evaluation
Sandeep Kumar, Shivani Jaiswal, Sukesh Kumar Gupta, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 9, pp. 4710-4729
Closed Access | Times Cited: 11
Potent carbonic anhydrase I, II, IX and XII inhibition activity of novel primary benzenesulfonamides incorporating bis-ureido moieties
Tuba Tekeli, Süleyman Akocak, Andrea Petreni, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2023) Vol. 38, Iss. 1
Open Access | Times Cited: 10
Phenolic Content Analysis of Two Species Belonging to the Lamiaceae Family: Antioxidant, Anticholinergic, and Antibacterial Activities
A.R. Ndhlala, Mesut Işık, Arzu Kavaz Yüksel, et al.
Molecules (2024) Vol. 29, Iss. 2, pp. 480-480
Open Access | Times Cited: 2
Antioxidant Effects and Potential Molecular Mechanism of Action of Diplocyclos palmatus (L.) C. Jeffrey Fruits Based on Systematic Network Pharmacology with Experimental Validation
Mitesh Patel, Lamya Ahmed Al‐Keridis, Sarah Owdah Alomrani, et al.
Journal of Molecular Structure (2024) Vol. 1313, pp. 138638-138638
Closed Access | Times Cited: 2
Synthesis, Theoretical, in Silico and in Vitro Biological Evaluation Studies of New Thiosemicarbazones as Enzyme Inhibitors
Musa Erdoğan, M. Serdar Çavuş, Halit Muğlu, et al.
Chemistry & Biodiversity (2023) Vol. 20, Iss. 11
Closed Access | Times Cited: 6
Design, synthesis, and biological evaluation of novel tryptanthrin derivatives as selective acetylcholinesterase inhibitors for the treatment of Alzheimer's disease
Jucheng Xia, Shuanghong Dong, Lili Yang, et al.
Bioorganic Chemistry (2023) Vol. 143, pp. 106980-106980
Closed Access | Times Cited: 6
Design and Synthesis of Pyrazole Carboxamide Derivatives as Selective Cholinesterase and Carbonic Anhydrase Inhibitors: Molecular Docking and Biological Evaluation
Mustafa Durgun, Süleyman Akocak, Nebih Lolak, et al.
Chemistry & Biodiversity (2023) Vol. 21, Iss. 2
Closed Access | Times Cited: 6
Nature of Luminescence and Pharmacological Activity of Sulfaguanidine
O. N. Tchaikovskaya, E. N. Bocharnikova, О. К. Базыль, et al.
Molecules (2023) Vol. 28, Iss. 10, pp. 4159-4159
Open Access | Times Cited: 5
Chemistry of heterocycles as carbonic anhydrase inhibitors: A pathway to novel research in medicinal chemistry review
Anjaneyulu Bendi, Taruna, Rajni Rajni, et al.
Archiv der Pharmazie (2024) Vol. 357, Iss. 7
Closed Access | Times Cited: 1
Naphthoquinones and anthraquinones: Exploring their impact on acetylcholinesterase enzyme activity
Hatice Esra Duran, Şükrü Beydemir
Biotechnology and Applied Biochemistry (2024) Vol. 71, Iss. 5, pp. 1079-1093
Open Access | Times Cited: 1
Synthesis of N-substituted 4-phenyl-2-aminothiazole derivatives and investigation of their inhibition properties against hCA I, II, and AChE enzymes
Abdullah Biçer, Cüneyt Çağlayan, Yeliz Demir, et al.
Archives of Biochemistry and Biophysics (2024) Vol. 761, pp. 110159-110159
Closed Access | Times Cited: 1
Identification of dilated cardiomyopathy‐linked key genes by bioinformatics methods and evaluating the impact of tannic acid and monosodium glutamate in rats
Habibe Karadaş, Hilal Tosun, Hamid Ceylan
Biotechnology and Applied Biochemistry (2024)
Open Access | Times Cited: 1
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