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OpenAlex Citation Counts

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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:

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

Showing 1-25 of 79 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
Synthesis and biological studies of pyrimidine derivatives targeting metabolic enzymes
Elif Korkusuz, Yusuf Sert, Seher Arslan, et al.
Archiv der Pharmazie (2024) Vol. 357, Iss. 8
Open Access | Times Cited: 17
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
Using deep learning and molecular dynamics simulations to unravel the regulation mechanism of peptides as noncompetitive inhibitor of xanthine oxidase
Yi He, Kaifeng Liu, Fuyan Cao, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 12
Insights into Manganese Superoxide Dismutase and Human Diseases
Mengfan Liu, Xueyang Sun, Boya Chen, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 24, pp. 15893-15893
Open Access | Times Cited: 58
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
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
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
N‐substituted phthalazine sulfonamide derivatives as non‐classical aldose reductase inhibitors
Cüneyt Türkeş, Mustafa Arslan, Yeliz Demir, et al.
Journal of Molecular Recognition (2022) Vol. 35, Iss. 12
Closed Access | Times Cited: 30
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
Methyl benzoate derivatives: in vitro Paraoxonase 1 inhibition and in silico studies
Işıl Nihan Korkmaz, Cüneyt Türkeş, Yeliz Demir, et al.
Journal of Biochemical and Molecular Toxicology (2022) Vol. 36, Iss. 10
Closed Access | Times Cited: 21
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
“Challenges and toxicity assessment of inorganic nanomaterials in biomedical applications: Current status and future roadmaps”
Pranjali Mahamuni‐Badiger, Maruti J. Dhanavade
Journal of Drug Delivery Science and Technology (2023) Vol. 87, pp. 104806-104806
Closed Access | Times Cited: 12
Neuroprotective activity of novel phenanthrene derivative from Grewia tiliaefolia by in vitro and in silico studies
Ankita Rajput, Palvi Sharma, Nitish Kumar, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 11
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
Identification of 1,3,4-oxadiazoles as tubulin-targeted anticancer agents: a combined field-based 3D-QSAR, pharmacophore model-based virtual screening, molecular docking, molecular dynamics simulation, and density functional theory calculation approach
Agnidipta Das, Manaswini Sarangi, Kailash Jangid, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 19, pp. 10323-10341
Closed Access | Times Cited: 11
Synthesis, biological evaluation and molecular docking of novel pyrazole derivatives as multitarget acetylcholinesterase and carbonic anhydrase inhibitors
Samet Mert, Yeliz Demir, Yusuf Sert, et al.
Journal of Molecular Structure (2024) Vol. 1319, pp. 139472-139472
Closed Access | Times Cited: 3
Establishing a link between the chemical composition and biological activities of Gladiolus italicus Mill. from the Turkish flora utilizing in vitro , in silico and network pharmacological methodologies
Gökhan Zengin, Mehmet Veysi Çetiz, Nurgül Abul, et al.
Toxicology Mechanisms and Methods (2024), pp. 1-21
Closed Access | Times Cited: 3
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